14 Jobs für Clinical Writer
Stellenangebote Clinical Writer Jobs
Job vor 3 Tagen bei Jobleads gefunden
• Berlin
Betriebliche Altersvorsorge
[. .. ] Stellen, Bevollmächtigten und internationalen Partnern Unterstützung bei Audits, Inspektionen und internen Qualitätsprojekten Dein 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 (EU2017/ 745) Erfahrung in der Erstellung und Pflege von Technischen Dokumentationen und Konformitätserklärungen Kenntnisse in PMS, Vigilanz und idealerweise in der Erstellung [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Basel- Stadt
[. .. ] About the Organization: Join IMP Quality Distribution, a critical function within Global Quality Assurance. We are responsible for maintaining the quality and compliance of Investigational Medicinal Products [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (IMP) throughout the clinical supply chain. Our team acts as the appointed Delegate of the Swiss Responsible Person (Fv P) and holds Global QA oversight over the entire IMP Distribution Network (Depots) and our key business counterpart, Global Clinical Supply Chain Management Distribution (PTDS-L) . We drive continuous improvement and ensure adherence to international [. .. ] . Proven and comprehensive experience (min. 3 years) in Quality Assurance with a strong focus on compliance. Deep knowledge of a regulated Gx P environment (GMP/ GDP) . Fluent speaker and writer in English (German is a plus) . Fluency is essential for managing critical regulatory documentation, providing authoritative guidance to European sites, and ensuring successful support during Health Authority Inspections. Nice to Haves Familiarity with Veeva vault QMS. Roche experience. PTQ experience. Experience in supplier management especially depots. Reference Nr. : [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Global Quality Manager
• Basel, Basel- Stadt
Homeoffice möglich
[. .. ] IMP Quality Distribution (PTQEAB) Team: 7 people Working Hours: Standard About the job The team is responsible for maintaining the quality and compliance of Investigational Medicinal Products [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (IMP) throughout the clinical supply chain and acts as the appointed Delegate of the Swiss Responsible Person (Fv P) and holds Global QA oversight over the entire IMP Distribution Network (Depots) and our key business counterparter, Global Clinical Supply Chain Management Distribution (PTDS-L) . They drive continuous improvement and ensure adherence to international GMP/ [. .. ] Biology, Engineering) Proven and comprehensive experience (min. 3 years) in Quality Assurance with a strong focus on compliance Deep knowledge of a regulated Gx P environment (GMP/ GDP) Fluent speaker and writer in English (German is a plus) . Fluency is essential for managing critical regulatory documentation, providing authoritative guidance to European sites, and ensuring successful support during Health Authority Inspections. Nice to Haves Familiarity with Veeva vault QMS PTQ experience Experience in supplier management especially depots Application Submission Deadline: 23.06. [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
[. .. ] d) . Background: Join IMP Quality Distribution, a critical function within Global Quality Assurance. We are responsible for maintaining the quality and compliance of Investigational Medicinal Products [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (IMP) throughout the clinical supply chain. Our team acts as the appointed Delegate of the Swiss Responsible Person (Fv P) and holds Global QA oversight over the entire IMP Distribution Network (Depots) and our key business counterpart Global Clinical Supply Chain Management Distribution (PTDS-L) . We drive continuous improvement and ensure adherence to international [. .. ] . Proven and comprehensive experience (minimum 3 years) in Quality Assurance with a strong focus on compliance. Deep knowledge of a regulated Gx P environment (GMP/ GDP) . Fluent speaker and writer in English (German is a plus) . Fluency is essential for managing critical regulatory documentation, providing authoritative guidance to European sites, and ensuring successful support during Health Authority Inspections. Nice to Haves Familiarity with Veeva vault QMS. Roche experience. PTQ experience. Experience in supplier management especially depots. Job Details Location: [. .. ]
Job am 05.06.2026 bei Jobleads gefunden
• Berlin
[. .. ] diabetes, and mental health. Founded in Australia in 2019, we have now helped over 500K patients globally by combining technology, design and operational excellence to help patients [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] access the best clinical support when they need it-wherever they are. Our 4 digital Clinics (Juniper, Pilot, Kin Software) focus heavily on personalising the experience for different demographics and are powered by a growing team across 5 countries (Australia, UK, Germany, Japan, and the Philippines) . Weve raised over AUD150M in funding from [. .. ] a passionate and caring patient support specialist to communicate with patients, doctors and manage consultation flows via our platform. We are seeking a bi-lingual 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. Responsible for onboarding new patients, proactively resolving patient tickets [. .. ]
Job am 24.05.2026 bei Jobleads gefunden
• Berlin
Teilzeit
Who we are Foundation models have transformed text and images, but structured data-the largest and most consequential data modality in the world-has remained untouched. Tables power every
clinical trial, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] every financial model, every scientific experiment, every business decision. No one has built a foundation model that truly understands them. Until now. What LLMs did for language, were doing for tables. The next modality shift in AI is happening-and were hiring the team that makes it. Momentum: We [. .. ]
Job am 16.05.2026 bei Jobleads gefunden
• Berlin
As a Medical
Writer, you are Flinns in-house
clinical documentation expert. You produce high quality clinical deliverables directly for our Med Tech customers across the full MDR/ IVDR [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lifecycle: Clinical Evaluation Reports (CERs) , Clinical Evaluation Plans (CEPs) , PMCF plans and reports, State of the Art (SOTA) reports, and PSURs. This is a generalist role by design: you [. .. ]
Job am 12.05.2026 bei Jobleads gefunden
• Baden- Württemberg
A well-established international medical device manufacturer with a strong reputation in diagnostic and
clinical solutions used across healthcare environments globally. The company operates within a highly regulated environment with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a strong quality culture and collaborative cross-functional structure across Regulatory Affairs, Quality, R D, and Clinical teams. The role opportunity This role reports to the Head of QA/ RA and is responsible for the [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 14.03.2026 bei Jobleads gefunden
• 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, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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 [. .. ]
Neu Job vor 3 Std. bei Neuvoo gefunden
Excelya
Senior Medical Writer (Europe)
• Freiburg, Baden- Wurttemberg
[. .. ] to 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Senior Medical Writer, based in Greece or France or Germany or Poland or Hungary or Belgium or Bulgaria for a full-time role, to provide medical and scientific expertise required for the successful completion of Excelyas projects. Your Mission: To write and edit complex medical writing deliverables (including informed consent forms, clinical study reports, clinical evaluation reports, CTD submissions) in accordance with sponsors and Excelyas SOPs, guidelines and applicable legislation. To coordinate cross-functional stakeholders and departments (including Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, PV) to ensure the timely collection, review, alignment, and integration of scientific and clinical content required for [. .. ]
Job vor 5 Tagen bei Neuvoo gefunden
Unora GmbH
Regulatory Affairs Manager (m/w/d) , Elternzeitvertretung für ca. 2 Jahre
• Berlin
Betriebliche Altersvorsorge
[. .. ] Stellen, Bevollmächtigten und internationalen Partnern Unterstützung bei Audits, Inspektionen und internen Qualitätsprojekten Dein 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 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
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
▶ Zur Stellenanzeige
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 14 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 Berlin (5 Jobs), Niedersachsen (2 Jobs) und Hamburg (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Writer Jobs?
Clinical Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
