16 Jobs für Clinical Writer
Stellenangebote Clinical Writer Jobs
Job am 22.08.2026 bei StepStone gefunden
Unora GmbH
• Berlin
Beratungs-/ Consultingtätigkeiten Teilzeit Homeoffice möglich
Betriebliche Altersvorsorge
[. .. ] Benannten Stellen, Bevollmächtigten und internationalen Partnern Unterstützung bei Audits, Inspektionen und internen Qualitätsprojekten Profil Abgeschlossenes naturwissenschaftliches, technisches oder regulatorisches Studium (z. B. Medizintechnik, Biowissenschaften, Regulatory Affairs) Nachweisbare [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Erfahrung als Medical Writer im Bereich Medical Devices-praktische Erfahrung beim Erstellen von Clinical Evaluation Plans (CEP) und Clinical Evaluation Reports (CER) Berufserfahrung im Bereich Regulatory Affairs oder Produktzulassung für Medizinprodukte Gute Kenntnisse der regulatorischen Anforderungen für Medizinprodukte der Klasse I gemäß MDR (EU 2017/ 745) Erfahrung in der Erstellung und Pflege von Technischen Dokumentationen und Konformitätserklärungen Kenntnisse in PMS, Vigilanz und idealerweise in [. .. ]
Job am 22.08.2026 bei Stellen-Online.de gefunden
Ideals
• Deutschland, 99986
Führungs-/ Leitungspositionen
[. .. ] 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, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] corporate reporting, licensing, clinical trials, and other complex transactions. Ideals Board: Board and leadership collaboration platform for faster, safer, and more compliant decision-making. The role Ideals has grown 2x in the past four years to a team of 500+ people across 30+ countries. The next stage is more ambitious: scaling toward unicorn status, [. .. ] 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 for your physical and mental health Funding for sports competitions Paid health-related time-off Extra perks Budget for local gatherings in global locations Generous internal referral program Our culture Commitment, Excellence, Collaboration, Trust and Care are core values to the [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Parexel International
• AT- 9 Wien
Führungs-/ Leitungspositionen
About Parexel Parexel is a leading global
clinical development partner delivering insightsdriven clinical and consulting solutions to the life sciences industry. With 22, 000+ employees worldwide, we partner with biopharmaceutical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] companies and research sites to design and deliver patientfocused clinical trials that broaden access and make research a care option for anyone, anywhere. We work with focus, agility, [. .. ] of vendor services (including Central Lab) in conjunction with other functions. In collaboration with other functions, ensures timely cleaning and delivery of clinical trial data. Coordinates and supports trial medical writer in providing the CTR. Responding for timely, complete and compliant archiving of all relevant global documents in the TMF, including all required documents from vendors. Support results/ documents disclosure of global registries. May support publication of trial data. Candidate Profile Youll thrive in this role if you bring: Extensive experience [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
IBSA Institut Biochimique SA
• AT- 2 Schweiz
Absolventen, Einsteiger, Trainees
IBSA Institut Biochimique SA cerca un professionista con esperienza in redazione scientifica e pubblicazioni, per trasporre risultati clinici in articoli e documenti regolatori. Si richiede esperienza diretta di medical writing, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] preferibilmente almeno due anni, nonch conoscenza di metodologia di ricerca clinica e GCP/ GLP. Collaborer con gruppi pre [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
[. .. ] of the Development Sciences department and organizational goals. Filling this need with a regular full-time employee will enable Bio Marin to reduce writing-related CRO and contractor costs, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] increase Clinical Medical Writing productivity to meet development needs, and realize efficiencies and consistent documentation quality across programs through repeatable processes and continuity of knowledge of programs, investigational products, and indications. The Principal Clinical Medical Writer has functional oversight responsibilities for medical writing staff and for the medical writing requirements for clinical development programs, including authoring/ editing documents. RESPONSIBILITIES: Oversight responsibilities for Medical Writing staff Works with the Head of Medical Writing to establish and maintain timelines for program planning. Drafts and edits documents used in [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
Führungs-/ Leitungspositionen
Serve as medical
writer and subject matter expert preparing
clinical regulatory documents through all phases of clinical research Execute the clinical trial transparency and disclosure book of work and provide [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] vendor oversight Collaborate with regulatory affairs, clinical development, clinical operations, biostatistics, pharmacology, translational research, manufacturing, and other crossfunctional teams Manage document review processes and resolve conflicting or ambiguous comments Establish [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
Lead the clear and accurate completion of medical writing deliverables Manage medical writing activities for individual studies across departments with minimal supervision Lead resolution of client comments Complete
clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] study protocols, protocol amendments, clinical study reports, patient narratives, annual reports, investigator brochures, informed consents, plain language summaries, periodic safety update reports, clinical development plans, IND submissions, integrated summary reports, NDA and e CTD submissions, journal manuscripts, abstracts, posters, and presentations Apply regulatory standards, company SOPs, client standards, approved templates, authorship [. .. ]
Job gestern bei Jobleads gefunden
[. .. ] team players, forward thinkers, and game changers. Are you looking for an inspiring career? You just found it. Job Overview Responsible for the generation and development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] documents relating to clinical evaluations and clinical investigations. This position is hybrid or fully remote in the US preferably on EST zone. This is a fixed term position with direct hire with Getinge with a high potential to convert to regular hire. Job Responsibilities and Essential Duties Serves as a clinical evaluation lead and [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• Hamburg
[. .. ] work proactively and think longterm-in operations, quality management, process optimization, product development and distribution. We are innovation drivers, possibility makers and a reliable partner, all in one. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (Senior) Manager Clinical Development (m/f/d) Date: Feb10, 2026 Location: Hamburg, DE, 20097 Business Unit: Pharma Job Function: Product Development/ Launch Management Level of Experience: Mid Career 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 [. .. ] 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 modules2.4 and2.5. In doing so, you respond to deficiency letters during registration procedures [. .. ]
Job am 02.09.2026 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 [. .. ]
Job am 30.08.2026 bei Jobleads gefunden
Patient Support Specialist, Germany
• Berlin
[. .. ] Juniper, one of the worlds largest weightmanagement programs combining GLP-1 medication with personalised nutrition, movement support, and clinicianled care from prescribers, nurses, health coaches, pharmacists, and dietitians. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. Our Growth Story: Supporting patients living with obesity across our 5 markets Received selective NICE endorsement to provide services to the NHS Tailored our offering to thousands [. .. ] and caring Patient support specialist (f/m/d) to communicate with patients, doctors and manage consultation flows via our platform. We are seeking a bilingual 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. This role may involve working on Saturdays as part [. .. ]
Job am 21.08.2026 bei Jobleads gefunden
Europe Regulatory Medical Writing Lead
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Revolution Medicines is seeking an experienced Principal Regulatory Medical
Writer to lead the preparation of regulatory documentation for
clinical development and marketing authorization across Europe. You will collaborate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with Regulatory Affairs, Clinical Development, and cross-functional teams to author, coordinate and finalize submissions. The role reports to the VP, Regulatory Affairs, Europe. You will serve as lead author for complex regulatory documents, ensuring scientific accuracy, #J-18808-Ljbffr [. .. ]
Job am 21.08.2026 bei Jobleads gefunden
Director, Principal Medical Writer, Europe
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Revolution Medicines is a late-stage
clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The companys R D pipeline comprises RAS (ON) inhibitors designed to suppress [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] diverse oncogenic variants of RAS proteins. The companys RAS (ON) inhibitors daraxonrasib (RMC-6236) , a RAS (ON) multi-selective inhibitor; elironrasib (RMC-6291) , a [. .. ] tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: As part of our expanding European organization, we are seeking an experienced Principal Regulatory Medical Writer to support the preparation of high-quality regulatory documentation for clinical development and marketing authorization activities across Europe. Working closely with Regulatory Affairs, Clinical Development, Clinical Operations, Biometrics, Pharmacovigilance, CMC, and other cross-functional teams, the successful candidate will author, coordinate and finalize regulatory documents supporting interactions with European and [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Lead Technical Writer for Medical Devices
• Bonaduz, Graubünden
Führungs-/ Leitungspositionen
[. .. ] Bonaduz, Switzerland, seeks a dedicated Team Lead for our information developers delivering end-user documentation for our devices and related products. You will lead a small team, collaborate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with engineering, clinical input, and regulatory bodies, ensuring on-time, high-quality documentation. Requirements include proven end-user documentation experience, ability to absorb complex procedures, and fluency in English with German willingness. #J-18808-Ljbffr 01428265 [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Junior Medical Writer: Clinical Publications Research
• Schweiz, Kärnten
Absolventen, Einsteiger, Trainees
IBSA Institut Biochimique SA cerca un professionista con esperienza in redazione scientifica e pubblicazioni, per trasporre risultati clinici in articoli e documenti regolatori. Si richiede esperienza diretta di medical writing, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] preferibilmente almeno due anni, nonch conoscenza di metodologia di ricerca clinica e GCP/ GLP. Collaborer con gruppi pre [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Medical Writer
• Hannover, Niedersachsen
[. .. ] assessment dossiers for pharmaceuticals within the AMNOG process and for EU Health Technology Assessments (HTA) in collaboration with clients. Perform scientific and statistical analysis, interpretation, gap analysis, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and presentation of clinical study results. Independently review scientific literature and prepare and document qualitative and quantitative analyses. Collaborate in interdisciplinary, agile teams composed of clients and colleagues. Apply stateoftheart, AIsupported technological solutions and New Work methods (e. g. , Design Thinking, SCRUM, Kanban) . Actively contribute to the continuous development of Kintiga. Receive [. .. ]
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 16 offene Stellenanzeigen für Clinical Writer Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Writer Jobs?
Aktuell suchen 5 Unternehmen nach Bewerbern für Clinical Writer Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Writer Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Writer Stellenangebote:
- Unora GmbH (1 Job)
- Ideals (1 Job)
- Parexel International (1 Job)
- IBSA Institut Biochimique SA (1 Job)
In welchen Bundesländern werden die meisten Clinical Writer Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Writer Jobs werden derzeit in Niedersachsen (2 Jobs), Berlin (2 Jobs) und Hamburg (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Writer Jobs?
Clinical Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
