14 Jobs für Clinical Research Writer
Stellenangebote Clinical Research Writer Jobs
Job vor 5 Tagen bei Jobleads gefunden
• 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 impeccable [...]
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[...] 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 vor 11 Tagen bei Jobleads gefunden
Medical Writer (m/w/d)
• 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 [...]
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[...] As a Medical Writer, you will play a key role in supporting the preparation and submission of AMNOG and JCA dossiers while contributing to GBA consultations and Joint Scientific Consultations (JSCs) . In this position, you will provide scientific expertise and assist with strategic planning to ensure highquality deliverables. Your responsibilities include contributing to [. .. ] (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 [. .. ] 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 09.12.2025 bei Jobleads gefunden
• Wiesbaden, Hessen
[. .. ] 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 [...]
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[...] 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 07.12.2025 bei Jobleads gefunden
• Berlin
Homeoffice möglich
Work-Life-Balance
Translational
Research in Oncology (TRIO) is a global academic
clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to bringing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the cancer treatments of the future to the patients of today. TRIO is seeking a Medical Writer to join our Medical Writing and Training team. This position reports to the Medical Writing Manager and is home-based in Germany. This position is a fixed-term role starting on March 2, 2026, and ending at the end of August 2026. Responsibilities Prepare, edit, and finalize trial-related documents, [. .. ]
Job am 05.12.2025 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 [...]
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[...] 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 22.11.2025 bei Jobleads gefunden
Director, Medical Writing, Oncology (1 of 2)
• 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 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 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 highlevel and crossfunctional TA meetings and has significant independent decisionmaking authority. Can step in for DU Head in case of absence. Is a [. .. ] key 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 #J-18808-Ljbffr 70303695 [. .. ]
Job am 06.11.2025 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] concentrates on delivering added value. This includes recruitment, supervision, and development of reports, as well as goal setting, performance assessment, task assignment, and budget. Key responsibilities Responsibilities [...]
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[...] as scientific medical writer including: Write, edit, and format a wide range of documents (of low to high 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 [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Work-Life-Balance
Overview 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 [...]
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[...] 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 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 09.10.2025 bei Jobleads gefunden
[. .. ] 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 [...]
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[...] 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 06.10.2025 bei Jobleads gefunden
Medical Writer
• Berlin
Abgeschlossenes Studium
Translational
Research in Oncology (TRIO) is a global academic
clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to bringing the cancer treatments of the future to the patients of today. TRIO is seeking a Medical Writer to join our Medical Writing and Training team. This position reports to the Medical Writing Manager and is home-based in Germany. This position is a fixed-term role starting on March 2, 2026, and ending at the end of August 2026. Responsibilities Prepare, edit, and finalize trial-related documents, [. .. ]
Job am 16.09.2025 bei Jobleads gefunden
Associate Director Scientific/ Medical Writing
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] and/or new definition of procedures is required. Key Responsibilities 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 [. .. ] and oncology. 5 years (handson) experience working in drug development in a therapeutically relevant field, preferably in oncology and/or immunology. 5 years (handson) experience as a scientific or medical writer in the pharmaceutical/ biotech industry. Prior experience drafting documents for multiple indications, preferably in Bio NTechrelevant indications. Prior experience drafting alone new or updated CTPs and CSRs required for Phase IIII trials. Prior experience drafting low to medium complexity variants of the following (new or updated variants) : IBs, clinical CTD modules, [. .. ]
Job am 05.07.2025 bei Jobleads gefunden
Software Medical Device Quality Engineer
• 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 [...]
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[...] 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 06.12.2025 bei Neuvoo gefunden
Abb Vie
Senior HTA Writer
• Wiesbaden, Hesse
Stellenbeschreibung 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. Zusätzliche Informationen [. .. ]
Job am 05.12.2025 bei Neuvoo gefunden
Translational Research in Oncology
Medical Writer
• Berlin
Homeoffice möglich
Work-Life-Balance
Translational
Research in Oncology (TRIO) is a global academic
clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to bringing the cancer treatments of the future to the patients of today. TRIO is seeking a Medical Writer to join our Medical Writing and Training team. This position reports to the Medical Writing Manager and is home-based in Germany. This position is a fixed-term role starting on March 2, 2026, and ending at the end of August 2026. Responsibilities: Prepare, edit, and finalize trial-related documents, [. .. ]
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 14 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 (4 Jobs), Rheinland-Pfalz (3 Jobs) und Hessen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Research Writer Jobs?
Clinical Research Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
