21 Jobs für Clinical Research Writer
Stellenangebote Clinical Research Writer Jobs
Job vor 10 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
[. .. ] Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Description The HTA Writer is responsible for providing clinical EUHTA document support to the JCA core team, ensuring successful preparation of high-quality submission-ready documents and effective implementation of the clinical writing process. Provides HTA writing expertise for multiple compounds and/or projects, expertise in HTA, oncology is a plus within a therapeutic area. Interfaces with JCA core [. .. ] skills, with a comprehensive knowledge of medical and scientific terminology across multiple therapeutic areas. Proficient in assimilating and analyzing complex data. Advanced understanding of HTA dossiers and HTA requirements, clinical research, study designs, biostatistics. Good understanding of regulatory requirements, and medical terminology cross functional teams and multiple contributors. Excellent English writing skills, effectively communicate and influence complex scientific and medical information to various stakeholders. Ability to collaborate with cross-functional teams. Strong organizational, time management, and problem-solving skills. Additional Information [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Principal Medical Writer
• München
[. .. ] projects Encourage and enable the continuous pursuit of quality service, creative ideas, and business success Support building a cohesive junior team through sound mentoring Essential Requirements: Degree [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] educated Demonstrate thorough research an understanding of the therapeutic area and scientific/ market environment Develop and deliver scientifically high quality content Strong understanding of the pharmaceutical drug development and approval process Desired Requirements: Ideally has relevant work experience and interest in healthcare industry Science Degree Experience of working on a digitally focused client account. [. .. ] generation agency group that offers the perfect combination of global size and unprecedented capabilities with European and local expertise. As a part of Syneos Health, a global biopharmaceutical accelerator integrating clinical development, real-world, late-stage and full commercialisation, we serve the complex European healthcare market with tailored communications solutions for our customers clinical and commercial success. W o r k H e r e M a t t e r s E v e r y w h e r [. .. ]
Job vor 11 Tagen bei Jooble gefunden
Biontech
• Mainz
Führungs-/ Leitungspositionen
[. .. ] make a meaningful difference in science and medicine. Your Contribution: With limited supervision/ guidance:-Write, edit, and format a wide range of documents (of low to high complexity) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] required for research, non-clinical, clinical development, and post-approval life cycle management largely according to standard procedures. Coordinate the document preparation, review, and approval. Check and revise documents with regard to scientific content, completeness, consistency, and standards compliance. Manage outsourced tasks: Plan, support So W set up, coordinate, and manage external writers providing medical writing [. .. ] knowledge in immunology and oncology. 5 years (hands-on) experience:-working in drug development in a therapeutically relevant field, preferably in oncology and/or immunology. as a scientific or medical writer in the pharmaceutical/ biotech industry. Prior experience:-drafting documents for multiple indications, preferably in Bio NTech-relevant indications. drafting alone new or updated CTPs and CSRs required for Phase I-III trials. drafting low to medium complexity variants of the following (new or updated variants) : IBs, clinical CTD modules, DSURs/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Principal Medical Writer
• München
[. .. ] projects Encourage and enable the continuous pursuit of quality service, creative ideas, and business success Support building a cohesive junior team through sound mentoring Essential Requirements: Degree [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] educated Demonstrate thorough research an understanding of the therapeutic area and scientific/ market environment Develop and deliver scientifically high quality content Strong understanding of the pharmaceutical drug development and approval process Desired Requirements: Ideally has relevant work experience and interest in healthcare industry Science Degree Experience of working on a digitally focused client account. [. .. ] generation agency group that offers the perfect combination of global size and unprecedented capabilities with European and local expertise. As a part of Syneos Health, a global biopharmaceutical accelerator integrating clinical development, real-world, late-stage and full commercialisation, we serve the complex European healthcare market with tailored communications solutions for our customers clinical and commercial success. W o r k H e r e M a t t e r s E v e r y w h e r [. .. ]
Neu Job vor 5 Std. bei Jobleads gefunden
• Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] problems related to the development and implementation of new service offerings and deliverables working independently to find effective solutions. Write or provide guidance to other writers on [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] all types of clinical regulatory and safety documents taking a proactive lead in content and scientific strategy with complete independence. Represent the MW department with decision-making authority in the R D organization leading discussions with senior cross-functional colleagues and external partners to enhance coordination between departments. Directly lead or set objectives for [. .. ] within the Medical Writing (MW) team in close consultation and accordance with the Delivery Unit (DU) Head and in line with R D priorities and TA objectives. Recognized expert medical writer for any document within and across TAs. Accountable for MW resource management and allocation within their portfolio (s) . Can represent MW DU Head or department at high-level and cross-functional TA meetings and has significant independent decision-making authority. Can step in for DU Head in case of [. .. ] for staff members. Shows openness to new ideas and fosters organizational learning. Required Skills Preferred Skills Required Experience Director Key Skills EMR Systems Post Residency Experience Occupational Health Experience Clinical Research Managed Care Primary Care Experience Medical Management Utilization Management Clinical Development Clinical Trials Leadership Experience Medicare Employment Type Full-Time Experience years Vacancy 1 #J-18808-Ljbffr 79877887 [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Manager, Strategic HTA Writer
• Wiesbaden, Hessen
Join to apply for the Strategic Medical
Writer role at Abb Vie. 3 days ago Be among the first 25 applicants. Company Description Abb Vies mission is to discover and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives [. .. ] eye care and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at Job Description The HTA Writer is responsible for providing clinical EUHTA document support to the JCA core team, ensuring successful preparation of highquality submissionready documents and effective implementation of the clinical writing process. Provides HTA writing expertise for multiple compounds and/or projects, expertise in HTA, oncology is a plus within a therapeutic area. Interfaces with JCA core and extended [. .. ] skills, with a comprehensive knowledge of medical and scientific terminology across multiple therapeutic areas. Proficient in assimilating and analyzing complex data. Advanced understanding of HTA dossiers and HTA requirements, clinical research, study designs, biostatistics. Good understanding of regulatory requirements, and medical terminology cross functional teams and multiple contributors. Excellent English writing skills, effectively communicate and influence complex scientific and medical information to various stakeholders. Ability to collaborate with crossfunctional teams. Strong organizational, time management, and problemsolving skills. Abb Vie is an [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Associate Director Scientific/ Medical Writing
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] make a meaningful difference in science and medicine. Your Contribution With limited supervision/ guidance: Write, edit, and format a wide range of documents (of low to high [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complexity) required for research, non-clinical, clinical development, and post-approval life cycle management largely according to standard procedures. Coordinate the document preparation, review, and approval. Check and revise documents with regard to scientific content, completeness, consistency, and standards compliance. Manage outsourced tasks: Plan, support So W set up, coordinate, and manage external writers providing medical writing [. .. ] knowledge in immunology and oncology. 5 years (hands-on) experience: working in drug development in a therapeutically relevant field, preferably in oncology and/or immunology. as a scientific or medical writer in the pharmaceutical/ biotech industry. Prior experience: drafting documents for multiple indications, preferably in Bio NTech-relevant indications. drafting alone new or updated CTPs and CSRs required for Phase I-III trials. drafting low to medium complexity variants of the following (new or updated variants) : IBs, clinical CTD modules, DSURs/ [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Global Clinical Trial Lead-Austria-Remote-FSP
Global
Clinical Trial Lead FSP Remote Parexel is actively recruiting for a Global Trial Manager/ Study Manager to join us in either Austria or Germany. In this role you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] will provide leadership and direction to the trial team and be accountable for the overall success and delivery of your assigned clinical trial [. .. ] implement amendments of core documents and training material updates/ retraining as needed. Support authority/ ethics responses as applicable. Ensure timely cleaning and delivery of clinical trial data, coordinating trial medical writer for CTR. Respond to timely, complete and compliant archiving of all relevant global documents in the TMF. Support results/ documents disclosure of global registries. Qualifications Bachelors degree and minimum 6 years of relevant global trial management experience. Technical proficiency in trial management systems and MS applications (Teams, MS Office, Project, [. .. ] understand and implement strategic direction and guidance for respective clinical studies. Effective communication skills via verbal, written, and presentation abilities. Seniority level Mid Senior level Employment type Fulltime Job functions Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing, Biotechnology Research, Hospitals and Health Care #J-18808-Ljbffr 78342375 [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• Hamburg
Homeoffice möglich
Flexible Arbeitszeiten Betriebliche Altersvorsorge Jobticket Work-Life-Balance
[. .. ] und flexible Arbeitszeiten gehören bei uns dazu Zuschuss zum HVV-Profi Ticket/ Deutschlandticket und zur betrieblichen Altersvorsorge Mitarbeiter Rabatte Tischtennisplatte und Billardtisch Remote Work Yes Employment Type Fulltime [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Key Skills Clinical Research, Adobe Acrobat, FDA Regulations, Technical Writing, Biotechnology, Clinical Development, Clinical Trials, Microsoft Powerpoint, Research Experience, Document Management Systems, Word Processing, Writing Skills Experience years Vacancy 1 #J-18808-Ljbffr 78130437 [. .. ]
Job am 24.01.2026 bei Jobleads gefunden
Patient Support Specialist, Germany
• Berlin
[. .. ] Juniper, one of the worlds largest weightmanagement programs that combines GLP1 medication with personalised nutrition, movement support, and clinicianled care from prescribers, nurses, health coaches, pharmacists, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] dietitians. Our published clinical research shows that our combined clinical and behavioural approach helps patients lose significantly more weight during their treatment with Juniper by four times. Growth Story 130 Yo Y revenue growth and a 90 reduction in cash burn, with 100M+ raised from investors including BOND, New View, Blackbird and Airtree. Scaled to over [. .. ] for a passionate and caring patient support specialist to communicate with patients, doctors, and manage consultation flows via our platform. You will be a bilingual German and English speaker and writer, triaging, managing and resolving patient support interactions. Onboard new patients, proactively resolve patient tickets, and make outbound calls to ensure we consistently deliver products and services above patient expectations. Work closely with our pharmacy, nurses and prescribers to ensure patients are informed and receive their orders in a timely and [. .. ]
Job am 23.01.2026 bei Jobleads gefunden
• Wien
[. .. ] edge AI-powered data analysis Services, that make it possible to standardize the process of skin imaging, objectify disease and treatment assessment, and to accelerate data collection and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analysis in clinical trials and medical routine. We are growing and seeking new, experienced and hands-on team members who think outside of the box, deliver unique ideas and like to work in a fast-paced digital health and medical research environment. You are reliable, ambitious, your heart beats for clinical trials, digital health and artificial intelligence. You like to prove yourself and like to work in an international team and highly collaborative job environment. Job Brief We are looking for an experiences Software Device Quality Engineer who is who develops [. .. ] Services Referrals increase your chances of interviewing at SCARLETRED Holding Gmb H by 2x Get notified about new Software Quality Engineer jobs in Vienna, Vienna, Austria. Senior Software Test Engineer Documentation Writer (w/m/d) Software Development Engineer in Test II Software Development Engineer in Test III (All Genders) JAVA Software Engineer-Test Automation (f/m/d) Full Stack Software Engineer-Med Tech Vienna or Remote (EU) Lead Golang Software Engineer, Commercial Systems Were unlocking community knowledge in a new way. Experts [. .. ]
Job am 23.01.2026 bei Jobleads gefunden
Principal Medical Writer
• Frankfurt, Hesse
Work-Life-Balance
ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our mission to shape the future of clinical development. We are currently seeking a Principal Medical Writer to join our diverse and dynamic team. As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. Your expertise in medical writing will be crucial in supporting our clients submissions to [. .. ]
Job am 18.01.2026 bei Jobleads gefunden
• Berlin
[. .. ] of the worlds largest weight-management programs combining GLP-1 medication with personalised nutrition, movement support, and clinician-led care from prescribers, nurses, health coaches, pharmacists, and dietitians. Our published [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical research shows that our combined clinical and behavioural approach helps patients lose significantly more weight during their treatment with Juniper by four times. Our Growth Story: 130 Yo Y revenue growth and a 90 reduction in cash burn, with 100M+ raised from investors including BOND, New View, Blackbird and Airtree. Scaled to [. .. ] a passionate and caring patient support specialist to communicate with patients, doctors and manage consultation flows via our platform. We are seeking a bi-lingual German and English speaker and writer to help triage, manage and resolve patient support interactions. Since our German market is still in its infant shoes with exciting growth plans over the next year, you will play an important role in shaping the team, culture and patient offering. Responsible for onboarding new patients, proactively resolving patient tickets [. .. ]
Job am 11.01.2026 bei Jobleads gefunden
Senior Grant Writer and Research Funding Lead
• Lausanne, Waadt
Führungs-/ Leitungspositionen
[. .. ] dynamic university campuses in Europe and ranks among the top 20 universities worldwide. The EPFL employs more than 6, 500 people supporting the three main missions of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the institution: education, research and innovation. The EPFL campus offers an exceptional working environment at the heart of a community of more than 17, 000 people, including over 12, 500 students and 4, 000 researchers from more than 120 different countries. Senior Grant Writer and Research Funding Lead The Laboratory for Intelligent Global Health and Humanitarian Response Technologies (Li GHT) at EPFL is seeking an experienced Senior Grant Writer and Research Funding Lead to support a rigorous, impactdriven research portfolio at the intersection of AI, medicine, and global health. This role is embedded in the scientific life of the lab. It focuses on strengthening research quality and coherence, supporting clinical and global health research, and enabling impact to scale through research itself. The position also includes scientific communication, translating complex research into clear written and visual narratives for funders and broader audiences. Mission The Laboratory for Intelligent Global Health and Humanitarian Response Technologies (Li GHT) is an impactdriven research group creating [. .. ]
Job am 11.01.2026 bei Jobleads gefunden
• Hannover, Niedersachsen
Medical
Writer (m/w/d) Market Access-Hannover, Germany (Hybride) Location: Hybrid (Office location: Hannover, Germany) Salary: Competitive, based on experience We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC) , [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a pan-European specialist consultancy that partners with ambitious health technology developers through the complex journey to achieve successful market [. .. ] (for further information: benefit assessment of pharmaceuticals) as well as EU Health Technology Assessments (HTA) in collaboration with our Clients Scientific and statistical analysis, interpretation, gap analysis, and presentation of clinical study results Independent review of scientific literature and preparation and documentation of qualitative and quantitative analyses Collaboration in interdisciplinary, agile teams composed of clients and colleagues Application of state-of-the-art, AI-supported technological solutions and New Work methods (e. g. , Design Thinking, SCRUM, Kanban) Active contribution to [. .. ] both languages Knowledge of the German healthcare system, the pharmaceutical market, and the relevant legal framework Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research Advanced skills in MS-Office CRM, project management, and data tools (preferred) , knowledge of La Te X is an advantage Strategic structured mindset, analytical thinking, numerical understanding and problem-solving ability Reliability and a meticulous client-oriented approach with a strong commitment to delivering highquality results Excellent organizational, agile and [. .. ]
Job am 19.12.2025 bei Jobleads gefunden
Medical Writer (m/w/d)
• Hannover, Niedersachsen
Beratungs-/ Consultingtätigkeiten
Are you looking for a fulltime position in a global strategic consultancy as a Medical
Writer to streamline patient access to lifechanging treatments through expert guidance, innovative tools, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] impeccable delivery? We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC) , a pan European specialist consultancy that partners with ambitious health technology developers through the complex journey to achieve successful market access across Europe, with [. .. ] (for further information: benefit assessment of pharmaceuticals) as well as EU Health Technology Assessments (HTA) in collaboration with our clients Scientific and statistical analysis, interpretation, gap analysis, and presentation of clinical study results Independent review of scientific literature and preparation and documentation of qualitative and quantitative analyses Collaboration in interdisciplinary, agile teams composed of clients and colleagues Application of stateoftheart, AIsupported technological solutions and New Work methods (e. g. , Design Thinking, SCRUM, Kanban) Active contribution to the continuous development of [. .. ] both languages Knowledge of the German healthcare system, the pharmaceutical market, and the relevant legal framework Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research Advanced skills in MS Office CRM, project management, and data tools (preferred) , knowledge of La Te X is an advantage Strategic structured mindset, analytical thinking, numerical understanding and problemsolving ability Reliability and a meticulous clientoriented approach with a strong commitment to delivering highquality results Excellent organizational, agile and classic project [. .. ]
Job am 13.12.2025 bei Jobleads gefunden
• Hannover, Niedersachsen
[. .. ] Become part of a supportive, dynamic team that thrives on innovation, lifelong learning, and making a meaningful impact in healthcare and life sciences. WHAT WERE LOOKING FOR [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As a Medical Writer, you will play a key role in supporting the preparation and submission of AMNOG and JCA dossiers while contributing to G-BA consultations and Joint Scientific Consultations (JSCs) . In this position, you will provide scientific expertise and assist with strategic planning to ensure high-quality deliverables. Your responsibilities include [. .. ] (for further information: benefit assessment of pharmaceuticals) as well as EU Health Technology Assessments (HTA) in collaboration with our clients Scientific and statistical analysis, interpretation, gap analysis, and presentation of clinical study results Independent review of scientific literature and preparation and documentation of qualitative and quantitative analyses Collaboration in interdisciplinary, agile teams composed of clients and colleagues Application of state-of-the-art, AI-supported technological solutions and New Work methods (e. g. , Design Thinking, SCRUM, Kanban) Active contribution to [. .. ] both languages Knowledge of the German healthcare system, the pharmaceutical market, and the relevant legal framework Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research Advanced skills in MS-Office CRM, project management, and data tools (preferred) , knowledge of La Te X is an advantage Strategic structured mindset, analytical thinking, numerical understanding and problem-solving ability Reliability and a meticulous client-oriented approach with a strong commitment to delivering high-quality results Excellent organizational, agile [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
Director, Medical Writing, Oncology (1 of 2)
• Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] problems related to the development and implementation of new service offerings and deliverables, working independently to find effective solutions. Write or provide guidance to other writers on [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] all types of clinical, regulatory and safety documents, taking a proactive lead in content and scientific strategy with complete independence. Represent the MW department with decisionmaking authority in the R D organization, leading discussions with senior crossfunctional colleagues and external partners to enhance coordination between departments. Directly lead or set objectives for team projects [. .. ] within the Medical Writing (MW) team in close consultation and accordance with the Delivery Unit (DU) . Head in line with R D priorities and TA objectives. Recognized expert medical writer for any document within and across TAs. Accountable for MW resource management and allocation within their portfolio (s) . Can represent MW DU Head or department at highlevel and crossfunctional TA meetings and has significant independent decisionmaking authority. Can step in for DU Head in case of absence. Is a [. .. ] business partners and customers. Creates a positive Credobased work environment for staff members. Shows openness to new ideas and fosters organizational learning. Required Skills : Preferred Skills Business Writing Clinical Research and Regulations Clinical Trials Operations Copy Editing Cross Functional Collaboration Developing Others Inclusive Leadership Industry Analysis Leadership Medical Affairs Medical Communications Performance Measurement Quality Validation Standard Operating Procedure (SOP) Succession Planning Tactical Planning Required Experience Director Key Skills Crisis Management, Marketing, Public Relations, Fundraising, Media Relations, Constant Contact, Strategic Planning, [. .. ]
Job am 28.10.2025 bei Jobleads gefunden
Director, Medical Writing, Oncology
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] problems related to the development and implementation of new service offerings and deliverables, working independently to find effective solutions. Write or provide guidance to other writers on [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] all types of clinical, regulatory, and safety documents, taking a proactive lead in content and scientific strategy with complete independence. Represent the MW department with decision-making authority in the R D organization, leading discussions with senior cross-functional colleagues and external partners to enhance coordination between departments. Directly lead or set objectives for [. .. ] within the Medical Writing (MW) team, in close consultation and accordance with the Delivery Unit (DU) Head and in line with R D priorities and TA objectives. Recognized expert medical writer for any document within and across TAs. Accountable for MW resource management and allocation within their portfolio (s) . Can represent MW DU Head or department at high-level and cross-functional TA meetings and has significant independent decision-making authority. Can step in for DU Head in case of [. .. ] business partners and customers. Creates a positive Credo-based work environment for staff members. Shows openness to new ideas and fosters organizational learning. Required Skills: Preferred Skills: Business Writing Clinical Research and Regulations Clinical Trials Operations Copy Editing Cross-Functional Collaboration Developing Others Inclusive Leadership Industry Analysis Leadership Medical Affairs Medical Communications Performance Measurement Quality Validation Standard Operating Procedure (SOP) Succession Planning Tactical Planning #J-18808-Ljbffr 67367925 [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Medical Science Liaison Hematology/ Oncology (m/f/d) - Rheinland-Pfalz, Saarland, Süd-Hessen, . . .
[. .. ] Oncology (m/f/d) Territory: Rheinland-Pfalz, Saarland, Süd-Hessen, Nordwest-Baden-Würtemberg Job Summary Medical Science Liaisons (MSLs) are a team of field-based, highly trained professionals with strong
clinical and/or scientific [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] backgrounds and excellent communication skills. They represent the Medical Affairs organization to the broad medical/ scientific community. Essential Functions Of The Job (Key Responsibilities) Represent the company and lead medical scientific exchanges within the respective community Develop and lead Key External Experts and investigators engagement plans-identify, [. .. ] you have any questions or concerns or would like to exercise your rights. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Incyte by 2x Get notified about new Medical Science Liaison jobs in Germany. Medical Science Liaison Oncology North Germany (Senior) Medical Affairs Scientist (m/w/d) Field Specialty Care: Inflammation Immunology, Gebiet: Bayern Medical Affairs Clinician-Southern Germany Austria Head of MSL Innovative Oncology DACH (m/w/d) Associate Director, Field Medical Advisor (m/w/d) Associate Director, Field Medical Advisor (m/w/d) Medical Writer/ Medical Content Manager (m/w/d) Principal Biostatistician (Medical Affairs/ HEOR-EMEA and NA Based) ) Medical Science Liaison-Germany (South) Cologne, North Rhine-Westphalia, Germany 5 days ago Medical Science Liaison Manager-NRW (m/f/d) Medical Science Liaison Oncology South West Germany Medical Science Liaison, Oncology, Germany (m/[. .. ]
Job am 13.01.2026 bei Neuvoo gefunden
ICON
Principal Medical Writer
• Frankfurt, Hessen
Work-Life-Balance
Principal Medical
Writer ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to join us on our mission to shape the future of clinical development. We are currently seeking a Principal Medical Writer to join our diverse and dynamic team. As a Principal Medical Writer at [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Research Writer pro Jahr?
Als Clinical Research Writer verdient man zwischen EUR 40.000,- bis EUR 65.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Research Writer Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 21 offene Stellenanzeigen für Clinical Research Writer Jobs.
In welchen Bundesländern werden die meisten Clinical Research Writer Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Research Writer Jobs werden derzeit in Niedersachsen (5 Jobs), Hessen (3 Jobs) und Sachsen-Anhalt (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Research Writer Jobs?
Clinical Research Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
