7 Jobs für Clinical Research Writer
Stellenangebote Clinical Research Writer Jobs
Job vor 4 Tagen bei Aktuelle TopJobs gefunden
Deutsche Rentenversicherung Baden- Württemberg
Sachbearbeiter/in Projektbüro (m/w/d)
• Karlsruhe oder Stuttgart
Sachbearbeiter/in Projektbüro (m/w/d) Deutsche Rentenversicherung Baden-Württemberg Karlsruhe oder Stuttgart Die Deutsche Rentenversicherung (DRV) Baden Württemberg ist einer der größten Regionalträger der gesetzlichen Rentenversicherung mit rund 3.600 Mitarbeitenden. Unsere Digitalisierungsabteilung stellt [...]
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[...] Anwenderinnen und Anwendern ein breit [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Frankfurt, Hesse
ICON Beijing/ Shanghai Sr. Medical
Writer ICON plc is a worldleading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we [...]
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[...] welcome you to join us on our mission to shape the future of clinical development. As a Senior Medical Writer at ICON, you will lead the development and execution of medical writing strategies for clinical research [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
FSP Principal Medical
Writer-Germany (m/f/d) Work Schedule: Standard (Mon-Fri) Environment: Office Job Summary We are expanding our Medical Writing FSP Team in Germany. This remote role will work from any [...]
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[...] location in Germany. The Principal Medical Writer will lead writing for a client in the FSP space, providing highquality medical and scientific documentation from planning and coordination through final drafts. The role includes reviewing documents, training junior writers, and advising on document strategy, regulations, and industry best practices. Key Responsibilities Research, write, and edit clinical study reports, study protocols, and data summaries. Serve as primary author for complex clinical and scientific documents (IBs, INDs, MAAs) and provide senior level review of routine and complex documents. Provide training and mentorship for writers and program managers on document preparation, software use, regulatory requirements, and therapeutic area knowledge. [. .. ]
Job am 27.03.2026 bei Jobleads gefunden
• 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 [...]
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[...] complexity) required for research, nonclinical, clinical development, and postapproval 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 services. Foster [. .. ] background knowledge in immunology and oncology. 5 years (handson) experience: working in drug development in a therapeutically relevant field, preferably in oncology and/or immunology. as a scientific and medical writer in the pharmaceutical/ biotech industry. Prior experience: drafting documents for multiple indications, preferably in Bio NTechrelevant indications. drafting alone new or updated CTPs and CSRs required for Phase IIII trials. drafting low to medium complexity variants of the following (new or updated variants) : IBs, clinical CTD modules, DSURs/ Annual Reports, [. .. ]
Job am 17.03.2026 bei Jobleads gefunden
• Frankfurt, Hesse
We are seeking a Principal Medical
Writer to support full
Clinical Study Report (CSR) writing for Phase 1, protocol development, and preparation of regulatory modules (2.7. 1/ 2.7. 2) . [...]
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[...] This role requires strong writing skills and attention to detail to ensure high-quality, inspectionready deliverables. Key Responsibilities Ensure all deliverables are inspectionready and compliant with regulatory and internal [. .. ] Proficient with Word templates and document formatting. Experience authoring Health Authority responses is required. Excellent communication skills (oral and written) in English. 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 https:/ / jobs. iqvia. com IQVIA is committed to integrity in [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] Canada Requisition Number: R-062453 Remote work options may be considered on a case-by-case basis and if approved by the Company. Purpose Able to function as a lead [...]
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[...] writer on any compound independently. Leads in setting functional tactics/ strategy. Leads project-level strategy (eg, submission team, global program team, clinical team) . May represent therapeutic area (TA) head at high-level and cross-functional TA meetings and has some independent decision-making authority. Able to write and coordinate complex documents within and across TAs independently. Contributes to and champions internal standards, regulatory, and publishing guidelines. Contributes to and champions the [. .. ] like to request an accommodation, please contact us via https:/ / or contact Ask GS to be directed to your accommodation resource. Required Skills Preferred Skills Analytics Insights 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 Team Management #J-18808-Ljbffr 83904548 [. .. ]
Job am 02.02.2026 bei Jobleads gefunden
• Wiesbaden, Hessen
[. .. ] areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at 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 [. .. ]
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 7 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 (1 Jobs), Rheinland-Pfalz (1 Jobs) und Hessen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Research Writer Jobs?
Clinical Research Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
