17 Jobs für Clinical Writer
Stellenangebote Clinical 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 [. .. ]
Job vor 3 Tagen bei StepStone gefunden
iDeals Solutions Germany GmbH
• Frankfurt
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] and make important decisions with less stress, higher quality, and shorter hours. Ideals Virtual Data Room (VDR) : Secure document sharing and collaboration for due diligence, fundraising, [...]
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[...] corporate reporting, licensing, clinical trials, and other complex transactions. The role Ideals has been in the Virtual Data Room space since 2008 and has built a trusted reputation with clients across multiple industries in Europe, including Orcan Energy, E-Group, Deloitte, and EY. We are looking for a Regional Head of Sales, to drive [. .. ] Academy with numerous courses Investment in external learning and development activities Guidance in Personal Development Plan creation Professional literature and subscriptions coverage Support of your passion as a speaker or writer Internal talent mobility opportunities For your well-being Tailored Wellness Package to support your physical and mental health Urban Sports membership Funding for sports competitions 30 business days of paid time off per year Paid health-related time off Extra perks Budget for local gatherings in global locations Generous internal [. .. ]
Job am 21.04.2026 bei Mindmatch.ai gefunden
Croma- Pharma
• AT- 3 Gemeinde Leobendorf
An international pharmaceutical company in Leobendorf is looking for an experienced regulatory
writer. The role involves writing
clinical and regulatory documents, ensuring compliance with EU regulations, and supporting global submissions. [...]
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[...] Required qualifications include a Masters degree in life sciences, at least 3 years of relevant experience, and strong English skills. The position offers flexible working hours, a competitive salary based on qualifications, and various employee benefits including professional [. .. ]
Job am 20.04.2026 bei Mindmatch.ai gefunden
Croma- Pharma
• AT- 3 Gemeinde Leobendorf
Homeoffice möglich
[. .. ] At CROMA Pharma, we are committed to developing and marketing innovative products that help our customers improve their wellbeing. Join us and grow with us. Responsibilities Write, [...]
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[...] review and maintain clinical and regulatory documents across the product lifecycle (e. g. Clinical Evaluation Plans and Reports, PMCF Plans and Reports, PSURs, Investigators Brochures) . Ensure compliance with applicable regulations and guidelines (EU MDR 2017/ 745, ICH-GCP, ISO 14155, FDA 21CFR) . Coordinate document review and approval processes, including comment reconciliation with [. .. ]
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 [. .. ]
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 [. .. ] 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 20.04.2026 bei Jobleads gefunden
Medical Writer (m/f/d)
• Gemeinde Leobendorf, Niederösterreich
Homeoffice möglich
[. .. ] At CROMA Pharma, we are committed to developing and marketing innovative products that help our customers improve their wellbeing. Join us and grow with us. Responsibilities Write, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] review and maintain clinical and regulatory documents across the product lifecycle (e. g. Clinical Evaluation Plans and Reports, PMCF Plans and Reports, PSURs, Investigators Brochures) . Ensure compliance with applicable regulations and guidelines (EU MDR 2017/ 745, ICH-GCP, ISO 14155, FDA 21CFR) . Coordinate document review and approval processes, including comment reconciliation with [. .. ]
Job am 20.04.2026 bei Jobleads gefunden
Regulatory Medical Writer Clinical Submissions (Hybrid)
• Gemeinde Leobendorf, Niederösterreich
An international pharmaceutical company in Leobendorf is looking for an experienced regulatory
writer. The role involves writing
clinical and regulatory documents, ensuring compliance with EU regulations, and supporting global [...]
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[...] submissions. Required qualifications include a Masters degree in life sciences, at least 3 years of relevant experience, and strong English skills. The position offers flexible working hours, a competitive salary based on qualifications, and various employee benefits including professional [. .. ]
Job am 03.04.2026 bei Jobleads gefunden
• München, Bayern
[. .. ] and make important decisions with less stress, higher quality, and shorter hours. Ideals Virtual Data Room (VDR) : Secure document sharing and collaboration for due diligence, fundraising, [...]
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[...] corporate reporting, licensing, clinical trials, and other complex transactions. The role Ideals is among the Top-5 of all companies on Rep Vue, as rated by Sales professionals. The Sales team has been a driving force behind our steady 30+ Yo Y growth, consistently generating millions in revenue. To support further expansion of the Ideals [. .. ] Academy with numerous courses Investment in external learning and development activities Guidance in Personal Development Plan creation Professional literature and subscriptions coverage Support of your passion as a speaker or writer Internal talent mobility opportunities For your well-being Tailored Wellness Package to support your physical and mental health Urban Sports membership Funding for sports competitions 30 business days of paid time off per year Paid health-related time off Extra perks Budget for local gatherings in global locations Generous internal [. .. ]
Job am 27.03.2026 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] 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) required [...]
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[...] 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
Principal Medical Writer Clinical Pharmacology (m/w/d)
• 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. [...]
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[...] 2) . 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 [. .. ]
Job am 14.03.2026 bei Jobleads gefunden
Sales Team Lead (Frankfurt, Germany)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] Room : A webbased cloud platform used by companies in a wide range of industries to ensure secure confidential document sharing for online due diligence, fundraising transactions, [...]
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[...] corporate reporting, licensing, clinical trials, and other business goals. The role We are looking for an Associate Director, Corporate Sales, to accelerate our growth as the firstchoice VDR provider in Germany. Based in Frankfurt and reporting to the Director of Business Development, Jens Hohnwald, youll lead a highperforming team to win new clients, expand [. .. ] Academy with numerous courses Investment in external learning and development activities Guidance in Personal Development Plan creation Professional literature and subscriptions coverage Support of your passion as a speaker or writer Internal talent mobility opportunities For your wellbeing Tailored Wellness Package to support your physical and mental health Urban Sports membership Funding for sports competitions 30 business days of paid time off per year Paid healthrelated time off Extra perks Teambuilding offline and online events Budget for local gatherings in global [. .. ]
Job am 13.03.2026 bei Jobleads gefunden
Business Development Account Executive (Frankfurt)
• Frankfurt, Hesse
[. .. ] Room : A webbased cloud platform used by companies in a wide range of industries to ensure secure confidential document sharing for online due diligence, fundraising transactions, [...]
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[...] corporate reporting, licensing, clinical trials, and other business goals. Ideals Board : A cloud platform with web and mobile applications used by board members, CEOs, executives, and corporate secretaries, to streamline governance and improve highstake decisions in a fast, secure, and compliant way. The role Ideals is among the Top5 of all companies on [. .. ] Academy with numerous courses. Investment in external learning and development activities. Guidance in Personal Development Plan creation. Professional literature and subscriptions coverage. Support of your passion as a speaker or writer. Internal talent mobility opportunities. For your wellbeing Tailored Wellness Package to support your physical and mental health. Urban Sports membership. Funding for sports competitions. 30 business days of paid time off per year. Paid healthrelated time off. Extra perks Teambuilding offline and online events. Budget for local gatherings in global [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Associate Director, Regulatory Medical Writing, Oncology
• 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 [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Business Development Account Executive (Frankfurt)
• München, Bayern
[. .. ] : A web-based cloud platform used by companies in a wide range of industries to ensure secure confidential document sharing for online due diligence, fundraising transactions, corporate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reporting, licensing, clinical trials, and other business goals. Ideals Board : A cloud platform with web and mobile applications used by board members, CEOs, executives, and corporate secretaries, to streamline governance and improve high-stake decisions in a fast, secure, and compliant way. The role Ideals is among the Top-5 of all [. .. ] Academy with numerous courses Investment in external learning and development activities Guidance in Personal Development Plan creation Professional literature and subscriptions coverage Support of your passion as a speaker or writer Internal talent mobility opportunities For your well-being Tailored Wellness Package to support your physical and mental health Urban Sports membership Funding for sports competitions 30 business days of paid time off per year Paid health-related time off Extra perks Team-building offline and online events Budget for local [. .. ]
Job am 02.02.2026 bei Jobleads gefunden
Manager, Strategic HTA Writer
• 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 [. .. ]
Job am 21.12.2025 bei Jobleads gefunden
Freelance Technical Writer (m/f/d) Medical Technology/ Regulatory Documentation
Freiberuflich
Freelance Technical
Writer (m/f/d) Medical Technology/ Regulatory Documentation Germany Freelance Technical Writer (m/f/d) Medical Technology/ Regulatory Documentation Remote Start: immediately Project-based/by arrangement About us We are an innovative Med [...]
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[...] Tech start-up (Cor Lector Gmb H) based in Nuremberg that develops software solutions for cardiology. Our products are [. .. ] create and maintain regulatory documents. Your tasks Creating, revising and maintaining technical documentation for MDR and FDA approvals. Structuring and editing documents such as instructions for use, risk management documents, clinical evaluations and software documentation. Working closely with the development, regulatory affairs and quality management departments. Ensuring compliance with applicable standards and regulatory requirements (e. g. ISO 13485, IEC 62304, ISO 14971) . Supporting the optimization of our documentation processes and structures. Your profile Several years of experience in technical writing, [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Writer pro Jahr?
Als Clinical Writer verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Writer Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 17 offene Stellenanzeigen für Clinical Writer Jobs.
In welchen Bundesländern werden die meisten Clinical Writer Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Writer Jobs werden derzeit in Bayern (2 Jobs), Niedersachsen (1 Jobs) und Rheinland-Pfalz (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Writer Jobs?
Clinical Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
