11 Jobs für Clinical Research Writer
Stellenangebote Clinical Research Writer Jobs
Job vor 9 Tagen 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 vor 10 Tagen bei Jobleads gefunden
Principal Medical Writer Clinical Pharmacology (m/w/d)
• Frankfurt, Hesse
Principal Medical
Writer Clinical Pharmacology (m/w/d) page is loaded # # Principal Medical Writer Clinical Pharmacology (m/w/d) locations: Frankfurt, Hesse, Germany: Dublin, Ireland: Paris, France: Madrid, Spaintime type: Full timeposted [...]
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[...] on: Posted Todaytime left to apply: End Date: June 5, 2026 (30+ days left to apply) job requisition id: R1521061 [. .. ] authoring Health Authority responses is required. + Proficient in Word templates and document formatting + 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 IQVIA is committed to integrity in our hiring process and maintains a [. .. ]
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 09.03.2026 bei Jobleads gefunden
• Freiburg im Breisgau, Baden- Württemberg
[. .. ] well as patient health and well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Global [...]
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[...] Medical Scientific Writer-70 part-time (m/f/d) . Dr. Falk Pharma is a research-based pharmaceutical company committed to bringing innovative new medicines to patients with gastroenterological and hepatic diseases. To bridge the divide from clinical research to clinical practice, we are looking for a qualified and motivated individual to translate clinical science for healthcare professionals, regulatory authorities, and other internal and external stakeholders. You are a healthcare enthusiast who is capable of adeptly assimilating and interpreting clinical efficacy and safety data or other scientific content [. .. ]
Job am 08.03.2026 bei Jobleads gefunden
Associate Director, Regulatory Medical Writing, Oncology
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] considered as a single submission. Remote work options may be considered on a case-by-case basis and if approved by the Company. Purpose Able to function as a [...]
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[...] lead 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 [. .. ] teach CREDO behaviors. Ability to act as change agent and adapt to rapidly changing organizational business challenges. Strong people management skills. 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 83335849 [. .. ]
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 [. .. ]
Neu Job vor 3 Std. bei Neuvoo gefunden
Excelya
Freiberuflich
[. .. ] step into a career-defining role in Medical Affairs. Ready to make an impact that travels the globe? Lets talk. About the Job We are seeking a Freelancer [...]
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[...] Senior Medical Writer, experienced with medical devices, for a part-time fully remote role, to provide medical and scientific expertise required for the successful completion of Excelyas projects. Your Mission: Lead the preparation and review of key medical device documentation, including PMCF plans/ reports, PSURs, CERs, and PMS reports for class IIA, IIB and III medical devices. Conduct comprehensive literature searches and critically appraise scientific data to support regulatory and clinical documentation. Provide expert medical and scientific input across projects, ensuring compliance with MDR requirements and supporting transitions from MDD to MDR. Respond to regulatory authority queries with clear, evidencebased medical justifications. Collaborate with crossfunctional teams to support studyrelated documentation (protocols, study reports) for medical device projects. Participate in scientific meetings [. .. ] medical devices. Proven experience with medical writing for various classes of medical devices, including preparation of PMCF, PSUR, CER, and PMS documentation. Ability to interpret, evaluate, and translate complex medical research findings into clear, structured content. Experience with literature search methodologies and critical appraisal of scientific evidence. Excellent written and verbal communication skills, with the ability to convey complex information effectively. Additional experience in IVD regulatory writing is considered an asset. Fluent in English. Knowledge of French language is a plus. [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
Abb Vie
Manager, Strategic HTA Writer
• Wiesbaden, Hesse
Job 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 11 Tagen bei Neuvoo gefunden
IQVIA
Principal Medical Writer Clinical Pharmacology (m/w/d)
• Frankfurt, Hessen
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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 2) . This role requires strong writing skills and attention to detail to ensure high-quality, inspection-ready deliverables. Key Responsibilities: Ensure all deliverables are inspection-ready and compliant with regulatory [. .. ] Experience authoring Health Authority responses is required. Proficient in Word templates and document formatting 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 IQVIA is committed to integrity in our hiring process and maintains [. .. ]
Job am 07.03.2026 bei Neuvoo gefunden
Dr. Falk Pharma GmbH
Global Medical Scientific Writer-70 part-time (m/f/d)
• Freiburg im Breisgau, Baden- Württemberg
[. .. ] and well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Dr. Falk Pharma [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] is a research-based pharmaceutical company committed to bringing innovative new medicines to patients with gastroenterological and hepatic diseases. To bridge the divide from clinical research to clinical practice, we are looking for a qualified and motivated individual to translate clinical science for healthcare professionals, regulatory authorities, and other internal and external stakeholders. You are a healthcare enthusiast who is capable of adeptly assimilating and interpreting clinical efficacy and safety data or other scientific content [. .. ]
Job am 27.02.2026 bei Neuvoo gefunden
HELM AG
(Senior) Clinical Trial Manager (m/f/d)
• Hamburg
At HELM Pharmaceuticals, based in the Headquarter in Hamburg, we develop generic pharmaceuticals. To strengthen our team in the Finished Dosage Form Programs we are looking for a Manager
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[...] class=highlight_text>Clinical Development (m/f/d) with a clinical life science background. In this position, you combine scientific expertise with strategic thinking, you help shape a highquality development pipeline and contribute to strong regulatory outcomes. You will work closely with interdisciplinary teams and external partners to drive projects forward efficiently. This role [. .. ] This also includes consultation and design of trial concepts with competent authorities and the preparation of scientific advice packages. Part of your role will also include tasks as a Medical
Writer, where you prepare and review scientific documentation on the efficacy and safety of our products. Here, you ensure the timely preparation of nonclinical and clinical documentation for regulatory submissions, including the commissioning and review of modules 2.4 and 2.5. In doing so, you respond to deficiency letters during [. .. ] due-diligence processes and evaluate dossiers as part of inlicensing activities. Your profile: You hold a university degree in a lifescience discipline. Moreover, you have a solid understanding of clinical
research with more than 3 years of experience. You combine scientific rigor with a handson mentality and a structured, solutionoriented way of working. You communicate effectively with interdisciplinary teams and external partners and feel comfortable managing several projects simultaneously. You are familiar with common IT applications within the framework of project [. .. ]
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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 11 offene Stellenanzeigen für Clinical Research Writer Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Research Writer Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Research Writer Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Research Writer Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Research Writer Stellenangebote:
- Excelya (1 Job)
- Abb Vie (1 Job)
- IQVIA (1 Job)
- Dr. Falk Pharma GmbH (1 Job)
- HELM AG (1 Job)
In welchen Bundesländern werden die meisten Clinical Research Writer Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Research Writer Jobs werden derzeit in Hessen (3 Jobs), Sachsen-Anhalt (2 Jobs) und Niedersachsen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Research Writer Jobs?
Clinical Research Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
