4 Ofertas de Redacción de Contenidos Atractivos en España
Administrativo/a de Calidad y Documentación Regulatoria
Publicado hace 2 días
Trabajo visto
Descripción Del Trabajo
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
**Creemos que la diversidad aporta valor a nuestro negocio, a nuestros equipos y a nuestra cultura. Estamos comprometidos con la igualdad de oportunidades y nuestra misión es ofrecer un entorno inclusivo donde las diferencias sumen a nuestra compañía.**
Ayúdanos a liderar una de las mayores empresas farmacéuticas del mundo. Somos un líder mundial en medicamentos derivados del plasma con presencia en más de 100 países y un equipo global en crecimiento de más de 20.000 personas. Por eso, necesitamos un/a **Administrativo/a** , **de Calidad y Asuntos Regulatorios** como tú.
**Misión del Rol**
Apoyar en la gestión administrativa del departamento de Calidad y Asuntos Regulatorios, asegurando el control y registro adecuado de las operaciones del área, contribuyendo al cumplimiento de las normativas internas y externas.
**Tus responsabilidades serán**
+ Realizarás la gestión administrativa de las reclamaciones y desviaciones recibidas que pudieran ser tanto de clientes internos de la empresa como de proveedores, así como puesta en mercado de lotes y trámites para la autorización de importación de medicamentos hemoderivados.
+ Proporcionarás ayuda en la revisión de la documentación regulatoria requerida para realizar el alta de materiales.
+ Te encargarás de la actualización y mantenimiento de los listados de control.
+ Realizarás tareas de organización y conservación del archivo de los documentos propios de la unidad organizativa.
+ Realizarás la gestión administrativa para la tramitación y seguimiento de la documentación requerida por clientes o concursos.
**Quién eres**
Para realizar este trabajo con éxito, una persona debe ser capaz de llevar a cabo las responsabilidades de manera satisfactoria. Los requisitos enumerados a continuación son representativos de los conocimientos, habilidades, formación y/o capacidad requeridos. Se pueden realizar adaptaciones del puesto para que las personas con diversidad funcional puedan realizar las tareas del puesto.
+ Posees un CFGM/CFGS en Análisis y Control de Calidad, Fabricación de Productos Farmacéuticos, Biotecnológicos y Afines, Química Industrial, Documentación y Administración Sanitarias o titulaciones equivalentes.
+ Se valorará formación complementaria en GMP, gestión documental, sistemas de calidad farmacéutica, asuntos regulatorios.
+ Posees un nivel de inglés intermedio B2.
+ Cuentas con 1 año de experiencia en posiciones similares. Se valorará experiencia en la gestión documental en industria farmacéutica; especialmente en áreas de asuntos regulatorio o de calidad.
+ Tienes un nivel intermedio de Excel (tablas dinámicas, macros, etc.) y de paquete Office.
+ Tienes experiencia y/o conocimientos de SAP (Valorable).
+ Eres una persona proactiva, organizada, detallista y con ganas en desarrollarte en un entorno farmacéutico documental.
**Lo que ofrecemos**
Formar parte de Grifols significa la oportunidad de trabajar en un entorno de proyección internacional dónde se promueve la igualdad de oportunidades.
Significa la oportunidad de desarrollarte profesionalmente, de disponer de formación continua y de integrarte en un equipo de profesionales en el que la aportación individual de cada uno cuenta. Nuestro compromiso es mantener un entorno que favorezca el desarrollo profesional de nuestros empleados en un buen ambiente de trabajo.
El capital humano de Grifols es clave tanto en el desarrollo de las actividades como en el proceso de expansión de la compañía.
Creemos en el talento diverso y queremos eliminar cualquier barrera que pueda impedir tu participación. Si necesitas algún ajuste en nuestro proceso de selección, por favor, no dudes en informarnos al aplicar. Estamos aquí para ayudarte.
**Horario flexible:** lunes - jueves 8:00h a 17:00h y viernes 8:00 a 15:00h.
**Paquete de beneficios**
**Contrato de trabajo:** Indefinido
**Flexibility for U Program:** 2 días de trabajo remoto
**Ubicación: Parets del Vallès**
more about Grifols
**Req ID:**
**Type:** Indefinido tiempo completo
**Job Category:** AREA TECNICA OPERACIONAL
**Creemos que la diversidad aporta valor a nuestro negocio, a nuestros equipos y a nuestra cultura. Estamos comprometidos con la igualdad de oportunidades y nuestra misión es ofrecer un entorno inclusivo donde las diferencias sumen a nuestra compañía.**
Ayúdanos a liderar una de las mayores empresas farmacéuticas del mundo. Somos un líder mundial en medicamentos derivados del plasma con presencia en más de 100 países y un equipo global en crecimiento de más de 20.000 personas. Por eso, necesitamos un/a **Administrativo/a** , **de Calidad y Asuntos Regulatorios** como tú.
**Misión del Rol**
Apoyar en la gestión administrativa del departamento de Calidad y Asuntos Regulatorios, asegurando el control y registro adecuado de las operaciones del área, contribuyendo al cumplimiento de las normativas internas y externas.
**Tus responsabilidades serán**
+ Realizarás la gestión administrativa de las reclamaciones y desviaciones recibidas que pudieran ser tanto de clientes internos de la empresa como de proveedores, así como puesta en mercado de lotes y trámites para la autorización de importación de medicamentos hemoderivados.
+ Proporcionarás ayuda en la revisión de la documentación regulatoria requerida para realizar el alta de materiales.
+ Te encargarás de la actualización y mantenimiento de los listados de control.
+ Realizarás tareas de organización y conservación del archivo de los documentos propios de la unidad organizativa.
+ Realizarás la gestión administrativa para la tramitación y seguimiento de la documentación requerida por clientes o concursos.
**Quién eres**
Para realizar este trabajo con éxito, una persona debe ser capaz de llevar a cabo las responsabilidades de manera satisfactoria. Los requisitos enumerados a continuación son representativos de los conocimientos, habilidades, formación y/o capacidad requeridos. Se pueden realizar adaptaciones del puesto para que las personas con diversidad funcional puedan realizar las tareas del puesto.
+ Posees un CFGM/CFGS en Análisis y Control de Calidad, Fabricación de Productos Farmacéuticos, Biotecnológicos y Afines, Química Industrial, Documentación y Administración Sanitarias o titulaciones equivalentes.
+ Se valorará formación complementaria en GMP, gestión documental, sistemas de calidad farmacéutica, asuntos regulatorios.
+ Posees un nivel de inglés intermedio B2.
+ Cuentas con 1 año de experiencia en posiciones similares. Se valorará experiencia en la gestión documental en industria farmacéutica; especialmente en áreas de asuntos regulatorio o de calidad.
+ Tienes un nivel intermedio de Excel (tablas dinámicas, macros, etc.) y de paquete Office.
+ Tienes experiencia y/o conocimientos de SAP (Valorable).
+ Eres una persona proactiva, organizada, detallista y con ganas en desarrollarte en un entorno farmacéutico documental.
**Lo que ofrecemos**
Formar parte de Grifols significa la oportunidad de trabajar en un entorno de proyección internacional dónde se promueve la igualdad de oportunidades.
Significa la oportunidad de desarrollarte profesionalmente, de disponer de formación continua y de integrarte en un equipo de profesionales en el que la aportación individual de cada uno cuenta. Nuestro compromiso es mantener un entorno que favorezca el desarrollo profesional de nuestros empleados en un buen ambiente de trabajo.
El capital humano de Grifols es clave tanto en el desarrollo de las actividades como en el proceso de expansión de la compañía.
Creemos en el talento diverso y queremos eliminar cualquier barrera que pueda impedir tu participación. Si necesitas algún ajuste en nuestro proceso de selección, por favor, no dudes en informarnos al aplicar. Estamos aquí para ayudarte.
**Horario flexible:** lunes - jueves 8:00h a 17:00h y viernes 8:00 a 15:00h.
**Paquete de beneficios**
**Contrato de trabajo:** Indefinido
**Flexibility for U Program:** 2 días de trabajo remoto
**Ubicación: Parets del Vallès**
more about Grifols
**Req ID:**
**Type:** Indefinido tiempo completo
**Job Category:** AREA TECNICA OPERACIONAL
¿Este trabajo es un acierto o un fracaso?
Postúlese Ahora
0
Descripción Del Trabajo
**Job Overview**
Performs quality control review of Medical Writing deliverables from internal and external authors to ensure accuracy, consistency, and compliance with format and style requirements. Provides leadership, training, and guidance to staff, and assists in resource management.
**Essential Functions**
+ Is a subject matter expert within the group and a source of advice and information to IQVIA staff on quality control processes;
+ Conduct quality control (QC) review of a wide range of Medical Writing deliverables for both internal and external customers, including complex and substantial documents, with limited guidance and consistent high quality and efficiency;
+ Document findings clearly, in accordance with defined procedures and checklists;
+ Liaise promptly with document authors in case of questions or missing sources;
+ Provide service metrics and scores, as required;
+ Develop quality tools such as checklists, quality guidelines, standards and scoring methodology to meet project specific needs;
+ May have responsibility for resourcing of QC tasks within the team;
+ Take a leading role in providing training, guidance, and mentoring within the QC group;
+ May take a formal supervisory role in managing QC staff and/or contract resources;
+ Take a leading role in proposing, developing, evaluating, and implementing process changes and tools and monitoring their adoption and benefits;
+ Take a leading role in QC team meetings and ensuring that lessons learned are shared and consistent approaches are applied;
+ Contribute to budget proposals for QC tasks and maintain a clear understanding of the time and resources needed for tasks within remit;
+ May take a leadership role for a stand-alone QC project, lead the team, and be the primary contact with the customer;
+ May participate in project team meetings and liaise directly with the customer on QC issues, as appropriate and with senior support as needed;
+ Take responsibility for on-time delivery of QC review comments;
+ Manage daily assignments, planning and directing work, and take responsibility for managing workload for assigned projects and tasks, in collaboration with senior staff;
+ Keep abreast of current data, trends, medical writing (MW)/regulatory knowledge, developments and advances in area of drug development/MW.
**Qualifications**
+ Bachelor's Degree Life sciences related discipline or related field Req
+ Master's Degree Life sciences related discipline or related field Pref
+ Ph.D. Life sciences related discipline or related field Pref
+ Typically, at least 8 years experience working with clinical trial documentation in a research environment, including significant experience of performing quality control (QC) review of clinical trial-related documents, defining and refining processes, and training and developing others.
**Experience**
+ Requires in-depth understanding of the structure, format, and purpose of a wide range of MW deliverables and the importance of consistency, clarity, and accuracy versus sources. Req
+ Careful attention to detail, accuracy, and consistency;
+ Impeccable English language skills and ability to detect and correct grammatical, spelling, and language errors;
+ Ability to understand scientific/medical documents and identify deficiencies, errors and inconsistencies;
+ Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents;
+ Proactivity and advanced organizational and time management skills and ability to prioritize workload effectively with commitment to deadlines;
+ Ability to communicate clearly, concisely, and effectively in English, both in writing and verbally, and confidence in using a range of communication methods to achieve results;
+ Good understanding of clinical drug development and the functions, steps, and processes involved;
+ Advanced understanding of the nature and purpose of Medical Writing deliverables;
+ Ability to provide clear and effective guidance and training in the form of written instructions, presentations, and one-to-one discussion;
+ Ability to provide thorough, appropriate, and sensitive feedback to less experienced colleagues;
+ Confident use of Microsoft Office and Adobe Acrobat;
+ Ability to quickly establish and maintain effective working relationships with co-workers, managers, and customers at a range of seniority levels.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Performs quality control review of Medical Writing deliverables from internal and external authors to ensure accuracy, consistency, and compliance with format and style requirements. Provides leadership, training, and guidance to staff, and assists in resource management.
**Essential Functions**
+ Is a subject matter expert within the group and a source of advice and information to IQVIA staff on quality control processes;
+ Conduct quality control (QC) review of a wide range of Medical Writing deliverables for both internal and external customers, including complex and substantial documents, with limited guidance and consistent high quality and efficiency;
+ Document findings clearly, in accordance with defined procedures and checklists;
+ Liaise promptly with document authors in case of questions or missing sources;
+ Provide service metrics and scores, as required;
+ Develop quality tools such as checklists, quality guidelines, standards and scoring methodology to meet project specific needs;
+ May have responsibility for resourcing of QC tasks within the team;
+ Take a leading role in providing training, guidance, and mentoring within the QC group;
+ May take a formal supervisory role in managing QC staff and/or contract resources;
+ Take a leading role in proposing, developing, evaluating, and implementing process changes and tools and monitoring their adoption and benefits;
+ Take a leading role in QC team meetings and ensuring that lessons learned are shared and consistent approaches are applied;
+ Contribute to budget proposals for QC tasks and maintain a clear understanding of the time and resources needed for tasks within remit;
+ May take a leadership role for a stand-alone QC project, lead the team, and be the primary contact with the customer;
+ May participate in project team meetings and liaise directly with the customer on QC issues, as appropriate and with senior support as needed;
+ Take responsibility for on-time delivery of QC review comments;
+ Manage daily assignments, planning and directing work, and take responsibility for managing workload for assigned projects and tasks, in collaboration with senior staff;
+ Keep abreast of current data, trends, medical writing (MW)/regulatory knowledge, developments and advances in area of drug development/MW.
**Qualifications**
+ Bachelor's Degree Life sciences related discipline or related field Req
+ Master's Degree Life sciences related discipline or related field Pref
+ Ph.D. Life sciences related discipline or related field Pref
+ Typically, at least 8 years experience working with clinical trial documentation in a research environment, including significant experience of performing quality control (QC) review of clinical trial-related documents, defining and refining processes, and training and developing others.
**Experience**
+ Requires in-depth understanding of the structure, format, and purpose of a wide range of MW deliverables and the importance of consistency, clarity, and accuracy versus sources. Req
+ Careful attention to detail, accuracy, and consistency;
+ Impeccable English language skills and ability to detect and correct grammatical, spelling, and language errors;
+ Ability to understand scientific/medical documents and identify deficiencies, errors and inconsistencies;
+ Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents;
+ Proactivity and advanced organizational and time management skills and ability to prioritize workload effectively with commitment to deadlines;
+ Ability to communicate clearly, concisely, and effectively in English, both in writing and verbally, and confidence in using a range of communication methods to achieve results;
+ Good understanding of clinical drug development and the functions, steps, and processes involved;
+ Advanced understanding of the nature and purpose of Medical Writing deliverables;
+ Ability to provide clear and effective guidance and training in the form of written instructions, presentations, and one-to-one discussion;
+ Ability to provide thorough, appropriate, and sensitive feedback to less experienced colleagues;
+ Confident use of Microsoft Office and Adobe Acrobat;
+ Ability to quickly establish and maintain effective working relationships with co-workers, managers, and customers at a range of seniority levels.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
¿Este trabajo es un acierto o un fracaso?
Postúlese Ahora
1
Descripción Del Trabajo
Senior Scientific Editor, Cell Genomics (Cell Press)
Do you have a minimum of 5 years editorial experience?
Do you have experience in editing scientific papers in genomics, genetics, or a related discipline, with a strong track record in publishing cutting‑edge genomic research and technologies?
Location: UK, Spain, Netherlands or China
About the Role
We are seeking an outstanding full-time Senior Scientific Editor to join the Cell Genomics team. We welcome applications from candidates with deep expertise in any area covered by the journal. Ideally, candidates will bring substantial editorial experience, a broad enthusiasm for science, and a strong interest in engaging with important advances across genetics and genomics. We are looking for someone who thrives in a fast-moving intellectual environment, can organize and prioritize across multiple responsibilities, and is excited by the opportunity to help shape research at the forefront of the field.
This is a full-time editorial position based in the United Kingdom, Spain, China or the Netherlands. Cell Genomics is a journal from Cell Press dedicated to publishing impactful studies across the breadth of genomics research, including work that advances understanding of genome function, the relationship between genotype and phenotype, computational and experimental methods, and related policy issues. As the journal continues to grow, this is an exceptional opportunity to join a dynamic editorial team and help define the scientific conversations that will shape the future of the field.
As a member of the Cell Genomics editorial team, you would play a central role in identifying and developing exciting science for publication. Responsibilities include recruiting strong submissions, evaluating research manuscripts, selecting expert referees, identifying timely emerging areas for commissioned content, and working closely with authors throughout the review process. The role also includes writing and editing content for the journal's website and social media channels, contributing to journal strategy, and representing genomics publishing across Cell Press.
This position offers the opportunity to engage closely with the global scientific community through travel and virtual visits to conferences and research institutions. You will meet leading researchers, learn about important new directions in the field, present the journal to diverse audiences, and bring those insights back to help inform editorial and strategic decisions. For a scientist who is energized by rigorous research, broad scientific engagement, and the chance to influence the field beyond a single laboratory, this role offers a uniquely rewarding next step.
Responsibilities
+ Evaluating submissions rigorously against the journals' requirements.
+ Support a culture of collaboration, creativity, and high standards. Your contribution will help a great team to reach new heights in serving the community.
+ Building global networks and commissioning exciting papers within the scope of the journal (including insightful front matter articles).
+ Working closely with the Cell Press editorial family, the production and operation team, as well as the business development and marketing team to support cross-journal initiatives and share best practices. Together, we serve the community better.
+ Representing Cell Genomics and Cell Press at conferences and public forums, showcasing the journal's impact and engaging with the broader scientific community. Your passion will inspire researchers and enable us to serve their needs.
+ Traveling to participate in domestic & international conferences and visiting research institutes to engage with researchers.
+ Collaborating with editorial teams of relevant Cell Press journals.
Requirements
+ A Ph.D. in any area related to the topics that Cell Genomics covers
+ At least 5 years of editorial experience
+ Ability to think critically about a wide range of scientific issues
+ Interest in engaging with the scientific community
+ Talent for distilling complex concepts and communicating them
+ Strong teamwork skills and a collaborative problem-solving mindset
+ Strong time management and organizational skills, with the ability to balance a range of priorities to achieve overall team goals
+ The ability to work well in diverse team settings
+ Have an interest in science communication and publishing trends
Your application must include a cover letter describing your interest in the position and how your skills and knowledge would further scientific communication and contribute to building the journal and advancing its mission. We will consider applications on a rolling basis until August 1st.
Work in a way that works for you
We promote a healthy work/life balance across the organisation. We offer an appealing working prospect for our people. With numerous wellbeing initiatives, shared parental leave, study assistance and sabbaticals, we will help you meet your immediate responsibilities and your long-term goals.
+ Working flexible hours - flexing the times when you work in the day to help you fit everything in and work when you are the most productive
Working for you
We know that your wellbeing and happiness are key to a long and successful career. These are some of the benefits we are delighted to offer:
+ Health Benefits: Comprehensive, multi-carrier program for medical, dental and vision benefits
+ Retirement Benefits: Access to a competitive contributory pension scheme
+ Wellbeing: Wellness platform with incentives, Headspace app subscription, Employee Assistance and Time-off Programs
+ Short-and-Long Term Disability, Life and Accidental Death Insurance, Critical Illness, and Hospital Indemnity
+ Family Benefits, including bonding and family care leaves, adoption and surrogacy benefits
+ Health Savings, Health Care, Dependent Care and Commuter Spending Accounts
+ Up to two days of paid leave each to participate in Employee Resource Groups and to volunteer with your charity of choice
About the Business
A global leader in information and analytics, we help researchers and healthcare professionals advance science and improve health outcomes for the benefit of society. Building on our publishing heritage, we combine quality information and vast data sets with analytics to support visionary science and research, health education and interactive learning, as well as exceptional healthcare and clinical practice. At Elsevier, your work contributes to the world's grand challenges and a more sustainable future. We harness innovative technologies to support science and healthcare to partner for a better world.
If performed in NLD Amsterdam (Radarweg), the base pay range is 68,670 - 114,450.
If performed in any of the following locations: Barcelona, Madrid, Home Based - Madrid, Home Based - Barcelona, the base pay range is 46,300 - 77,000.
This job may be subject to a collective labor agreement in Spain. Please consult with the hiring team for further details.
This job may be subject to a collective labor agreement in the Netherlands. Please consult with the hiring team for further details.
We know your well-being and happiness are key to a long and successful career. We are delighted to offer country specific benefits. Click here ( to access benefits specific to your location.
We are committed to providing a fair and accessible hiring process. If you have a disability or other need that requires accommodation or adjustment, please let us know by completing our Applicant Request Support Form or please contact .
Criminals may pose as recruiters asking for money or personal information. We never request money or banking details from job applicants. Learn more about spotting and avoiding scams here.
Please read our Candidate Privacy Policy.
We are an equal opportunity employer: qualified applicants are considered for and treated during employment without regard to race, color, creed, religion, sex, national origin, citizenship status, disability status, protected veteran status, age, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law.
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RELX is a global provider of information-based analytics and decision tools for professional and business customers, enabling them to make better decisions, get better results and be more productive.
Our purpose is to benefit society by developing products that help researchers advance scientific knowledge; doctors and nurses improve the lives of patients; lawyers promote the rule of law and achieve justice and fair results for their clients; businesses and governments prevent fraud; consumers access financial services and get fair prices on insurance; and customers learn about markets and complete transactions.
Our purpose guides our actions beyond the products that we develop. It defines us as a company. Every day across RELX our employees are inspired to undertake initiatives that make unique contributions to society and the communities in which we operate.
Do you have a minimum of 5 years editorial experience?
Do you have experience in editing scientific papers in genomics, genetics, or a related discipline, with a strong track record in publishing cutting‑edge genomic research and technologies?
Location: UK, Spain, Netherlands or China
About the Role
We are seeking an outstanding full-time Senior Scientific Editor to join the Cell Genomics team. We welcome applications from candidates with deep expertise in any area covered by the journal. Ideally, candidates will bring substantial editorial experience, a broad enthusiasm for science, and a strong interest in engaging with important advances across genetics and genomics. We are looking for someone who thrives in a fast-moving intellectual environment, can organize and prioritize across multiple responsibilities, and is excited by the opportunity to help shape research at the forefront of the field.
This is a full-time editorial position based in the United Kingdom, Spain, China or the Netherlands. Cell Genomics is a journal from Cell Press dedicated to publishing impactful studies across the breadth of genomics research, including work that advances understanding of genome function, the relationship between genotype and phenotype, computational and experimental methods, and related policy issues. As the journal continues to grow, this is an exceptional opportunity to join a dynamic editorial team and help define the scientific conversations that will shape the future of the field.
As a member of the Cell Genomics editorial team, you would play a central role in identifying and developing exciting science for publication. Responsibilities include recruiting strong submissions, evaluating research manuscripts, selecting expert referees, identifying timely emerging areas for commissioned content, and working closely with authors throughout the review process. The role also includes writing and editing content for the journal's website and social media channels, contributing to journal strategy, and representing genomics publishing across Cell Press.
This position offers the opportunity to engage closely with the global scientific community through travel and virtual visits to conferences and research institutions. You will meet leading researchers, learn about important new directions in the field, present the journal to diverse audiences, and bring those insights back to help inform editorial and strategic decisions. For a scientist who is energized by rigorous research, broad scientific engagement, and the chance to influence the field beyond a single laboratory, this role offers a uniquely rewarding next step.
Responsibilities
+ Evaluating submissions rigorously against the journals' requirements.
+ Support a culture of collaboration, creativity, and high standards. Your contribution will help a great team to reach new heights in serving the community.
+ Building global networks and commissioning exciting papers within the scope of the journal (including insightful front matter articles).
+ Working closely with the Cell Press editorial family, the production and operation team, as well as the business development and marketing team to support cross-journal initiatives and share best practices. Together, we serve the community better.
+ Representing Cell Genomics and Cell Press at conferences and public forums, showcasing the journal's impact and engaging with the broader scientific community. Your passion will inspire researchers and enable us to serve their needs.
+ Traveling to participate in domestic & international conferences and visiting research institutes to engage with researchers.
+ Collaborating with editorial teams of relevant Cell Press journals.
Requirements
+ A Ph.D. in any area related to the topics that Cell Genomics covers
+ At least 5 years of editorial experience
+ Ability to think critically about a wide range of scientific issues
+ Interest in engaging with the scientific community
+ Talent for distilling complex concepts and communicating them
+ Strong teamwork skills and a collaborative problem-solving mindset
+ Strong time management and organizational skills, with the ability to balance a range of priorities to achieve overall team goals
+ The ability to work well in diverse team settings
+ Have an interest in science communication and publishing trends
Your application must include a cover letter describing your interest in the position and how your skills and knowledge would further scientific communication and contribute to building the journal and advancing its mission. We will consider applications on a rolling basis until August 1st.
Work in a way that works for you
We promote a healthy work/life balance across the organisation. We offer an appealing working prospect for our people. With numerous wellbeing initiatives, shared parental leave, study assistance and sabbaticals, we will help you meet your immediate responsibilities and your long-term goals.
+ Working flexible hours - flexing the times when you work in the day to help you fit everything in and work when you are the most productive
Working for you
We know that your wellbeing and happiness are key to a long and successful career. These are some of the benefits we are delighted to offer:
+ Health Benefits: Comprehensive, multi-carrier program for medical, dental and vision benefits
+ Retirement Benefits: Access to a competitive contributory pension scheme
+ Wellbeing: Wellness platform with incentives, Headspace app subscription, Employee Assistance and Time-off Programs
+ Short-and-Long Term Disability, Life and Accidental Death Insurance, Critical Illness, and Hospital Indemnity
+ Family Benefits, including bonding and family care leaves, adoption and surrogacy benefits
+ Health Savings, Health Care, Dependent Care and Commuter Spending Accounts
+ Up to two days of paid leave each to participate in Employee Resource Groups and to volunteer with your charity of choice
About the Business
A global leader in information and analytics, we help researchers and healthcare professionals advance science and improve health outcomes for the benefit of society. Building on our publishing heritage, we combine quality information and vast data sets with analytics to support visionary science and research, health education and interactive learning, as well as exceptional healthcare and clinical practice. At Elsevier, your work contributes to the world's grand challenges and a more sustainable future. We harness innovative technologies to support science and healthcare to partner for a better world.
If performed in NLD Amsterdam (Radarweg), the base pay range is 68,670 - 114,450.
If performed in any of the following locations: Barcelona, Madrid, Home Based - Madrid, Home Based - Barcelona, the base pay range is 46,300 - 77,000.
This job may be subject to a collective labor agreement in Spain. Please consult with the hiring team for further details.
This job may be subject to a collective labor agreement in the Netherlands. Please consult with the hiring team for further details.
We know your well-being and happiness are key to a long and successful career. We are delighted to offer country specific benefits. Click here ( to access benefits specific to your location.
We are committed to providing a fair and accessible hiring process. If you have a disability or other need that requires accommodation or adjustment, please let us know by completing our Applicant Request Support Form or please contact .
Criminals may pose as recruiters asking for money or personal information. We never request money or banking details from job applicants. Learn more about spotting and avoiding scams here.
Please read our Candidate Privacy Policy.
We are an equal opportunity employer: qualified applicants are considered for and treated during employment without regard to race, color, creed, religion, sex, national origin, citizenship status, disability status, protected veteran status, age, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law.
USA Job Seekers:
EEO Know Your Rights.
RELX is a global provider of information-based analytics and decision tools for professional and business customers, enabling them to make better decisions, get better results and be more productive.
Our purpose is to benefit society by developing products that help researchers advance scientific knowledge; doctors and nurses improve the lives of patients; lawyers promote the rule of law and achieve justice and fair results for their clients; businesses and governments prevent fraud; consumers access financial services and get fair prices on insurance; and customers learn about markets and complete transactions.
Our purpose guides our actions beyond the products that we develop. It defines us as a company. Every day across RELX our employees are inspired to undertake initiatives that make unique contributions to society and the communities in which we operate.
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Descripción Del Trabajo
Senior Editor - The Lancet's eBioMedicine
Full time fixed term contract target end date: 31/05/2027
Location: Spain
Would you like to join the Lancet's family of world-renowned medical research journals?
Do you enjoy driving change with science?
About our Team
eBioMedicine is The Lancet's translational medicine journal and a leading open-access forum for basic and clinical biomedical research.
We are a collaborative, international team, handling high-quality research, review, and perspective submissions with a focus on rigorous peer review, ethics, and reproducibility. We seek to drive thought leadership in translational research by building solid relationships with research communities and ensuring we offer exciting, thought-provoking content.
At eBioMedicine, we are deeply committed to fostering a diverse, equitable, and inclusive environment. In our pursuit of excellence, we recognise the strength in varied perspectives, experiences, and backgrounds. As part of our ongoing efforts to enhance the diversity of our editorial team, we encourage applications from individuals who bring unique skills, backgrounds, and perspectives to the role.
About the Role
As an In-House Senior Editor for eBioMedicine, you will oversee the peer-review and publication of original content. You will identify experts to act as peer reviewers to ensure we publish high-quality content. Your attention to detail and ability to prioritise tasks will be critical in maintaining our standards. You will build global relationships with people and institutes in the translational research community to identify new material, authors, subject experts, and content opportunities.
Responsibilities
+ Arranging peer-review and commissioning content to ensure the successful and timely publication of high-quality translational research;
+ Staying up to date with the latest literature and research developments;
+ Engaging in conferences and academic meetings, along with site visits to develop and maintain links with the international research community;
+ Writing editorials, commissioning reviews and commentaries and publishing correspondence to build the journal's profile among the communities we serve;
+ Subediting material from all sections of our journal to improve clarity of expression and to conform to journal style.
Requirements
+ Higher degree in a relevant discipline with postdoctoral research experience or previous editorial experience;
+ Ability to communicate fairly and constructively with members of the translational research community;
+ Demonstrate broad knowledge of biological and medical sciences;
+ Have an exceptional command of the English language and the ability to write in an engaging manner;
+ Be able to travel internationally for meetings and conferences.
Work in a way that works for you
We promote a healthy work/life balance across the organisation. We offer an appealing working prospect for our people. With numerous wellbeing initiatives, shared parental leave, study assistance and sabbaticals, we will help you meet your immediate responsibilities and your long-term goals.
For this particular role, we do not expect daily attendance in the office. You will have a clearly defined schedule of work, and the way you use your weekly hours to complete it will be up to you.
About the Business
A global leader in information and analytics, we help researchers and healthcare professionals advance science and improve health outcomes for the benefit of society. Building on our publishing heritage, we combine quality information and vast data sets with analytics to support visionary science and research, health education and interactive learning, as well as exceptional healthcare and clinical practice. At Elsevier, your work contributes to the world's grand challenges and a more sustainable future. We harness innovative technologies to support science and healthcare to partner for a better world.
Primary Location Base Pay Range: Home Based - Spain 36,400 - 60,600.
If performed in any of the following locations: Barcelona, Madrid, Home Based - Madrid, Home Based - Barcelona, the base pay range is 38,300 - 63,600.
This role is covered by the Convenio Colectivo (Publishing sector convenio).
We know your well-being and happiness are key to a long and successful career. We are delighted to offer country specific benefits. Click here ( to access benefits specific to your location.
We are committed to providing a fair and accessible hiring process. If you have a disability or other need that requires accommodation or adjustment, please let us know by completing our Applicant Request Support Form or please contact .
Criminals may pose as recruiters asking for money or personal information. We never request money or banking details from job applicants. Learn more about spotting and avoiding scams here.
Please read our Candidate Privacy Policy.
We are an equal opportunity employer: qualified applicants are considered for and treated during employment without regard to race, color, creed, religion, sex, national origin, citizenship status, disability status, protected veteran status, age, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law.
USA Job Seekers:
EEO Know Your Rights.
RELX is a global provider of information-based analytics and decision tools for professional and business customers, enabling them to make better decisions, get better results and be more productive.
Our purpose is to benefit society by developing products that help researchers advance scientific knowledge; doctors and nurses improve the lives of patients; lawyers promote the rule of law and achieve justice and fair results for their clients; businesses and governments prevent fraud; consumers access financial services and get fair prices on insurance; and customers learn about markets and complete transactions.
Our purpose guides our actions beyond the products that we develop. It defines us as a company. Every day across RELX our employees are inspired to undertake initiatives that make unique contributions to society and the communities in which we operate.
Full time fixed term contract target end date: 31/05/2027
Location: Spain
Would you like to join the Lancet's family of world-renowned medical research journals?
Do you enjoy driving change with science?
About our Team
eBioMedicine is The Lancet's translational medicine journal and a leading open-access forum for basic and clinical biomedical research.
We are a collaborative, international team, handling high-quality research, review, and perspective submissions with a focus on rigorous peer review, ethics, and reproducibility. We seek to drive thought leadership in translational research by building solid relationships with research communities and ensuring we offer exciting, thought-provoking content.
At eBioMedicine, we are deeply committed to fostering a diverse, equitable, and inclusive environment. In our pursuit of excellence, we recognise the strength in varied perspectives, experiences, and backgrounds. As part of our ongoing efforts to enhance the diversity of our editorial team, we encourage applications from individuals who bring unique skills, backgrounds, and perspectives to the role.
About the Role
As an In-House Senior Editor for eBioMedicine, you will oversee the peer-review and publication of original content. You will identify experts to act as peer reviewers to ensure we publish high-quality content. Your attention to detail and ability to prioritise tasks will be critical in maintaining our standards. You will build global relationships with people and institutes in the translational research community to identify new material, authors, subject experts, and content opportunities.
Responsibilities
+ Arranging peer-review and commissioning content to ensure the successful and timely publication of high-quality translational research;
+ Staying up to date with the latest literature and research developments;
+ Engaging in conferences and academic meetings, along with site visits to develop and maintain links with the international research community;
+ Writing editorials, commissioning reviews and commentaries and publishing correspondence to build the journal's profile among the communities we serve;
+ Subediting material from all sections of our journal to improve clarity of expression and to conform to journal style.
Requirements
+ Higher degree in a relevant discipline with postdoctoral research experience or previous editorial experience;
+ Ability to communicate fairly and constructively with members of the translational research community;
+ Demonstrate broad knowledge of biological and medical sciences;
+ Have an exceptional command of the English language and the ability to write in an engaging manner;
+ Be able to travel internationally for meetings and conferences.
Work in a way that works for you
We promote a healthy work/life balance across the organisation. We offer an appealing working prospect for our people. With numerous wellbeing initiatives, shared parental leave, study assistance and sabbaticals, we will help you meet your immediate responsibilities and your long-term goals.
For this particular role, we do not expect daily attendance in the office. You will have a clearly defined schedule of work, and the way you use your weekly hours to complete it will be up to you.
About the Business
A global leader in information and analytics, we help researchers and healthcare professionals advance science and improve health outcomes for the benefit of society. Building on our publishing heritage, we combine quality information and vast data sets with analytics to support visionary science and research, health education and interactive learning, as well as exceptional healthcare and clinical practice. At Elsevier, your work contributes to the world's grand challenges and a more sustainable future. We harness innovative technologies to support science and healthcare to partner for a better world.
Primary Location Base Pay Range: Home Based - Spain 36,400 - 60,600.
If performed in any of the following locations: Barcelona, Madrid, Home Based - Madrid, Home Based - Barcelona, the base pay range is 38,300 - 63,600.
This role is covered by the Convenio Colectivo (Publishing sector convenio).
We know your well-being and happiness are key to a long and successful career. We are delighted to offer country specific benefits. Click here ( to access benefits specific to your location.
We are committed to providing a fair and accessible hiring process. If you have a disability or other need that requires accommodation or adjustment, please let us know by completing our Applicant Request Support Form or please contact .
Criminals may pose as recruiters asking for money or personal information. We never request money or banking details from job applicants. Learn more about spotting and avoiding scams here.
Please read our Candidate Privacy Policy.
We are an equal opportunity employer: qualified applicants are considered for and treated during employment without regard to race, color, creed, religion, sex, national origin, citizenship status, disability status, protected veteran status, age, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law.
USA Job Seekers:
EEO Know Your Rights.
RELX is a global provider of information-based analytics and decision tools for professional and business customers, enabling them to make better decisions, get better results and be more productive.
Our purpose is to benefit society by developing products that help researchers advance scientific knowledge; doctors and nurses improve the lives of patients; lawyers promote the rule of law and achieve justice and fair results for their clients; businesses and governments prevent fraud; consumers access financial services and get fair prices on insurance; and customers learn about markets and complete transactions.
Our purpose guides our actions beyond the products that we develop. It defines us as a company. Every day across RELX our employees are inspired to undertake initiatives that make unique contributions to society and the communities in which we operate.
¿Este trabajo es un acierto o un fracaso?
Postúlese Ahora
3