Clinical Writer Stellenangebote


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17 Jobs für Clinical Writer


Stellenangebote Clinical Writer Jobs


Job am 11.11.2025 bei JobMESH gefunden CGM Clinical Europe GmbH

Technical Writer (m/w/d)

• Bayern Sankt Wolfgang Abgeschlossenes Studium Deine Aufgabe bei CGM: Als führendes Unternehmen im Bereich Softwarelösungen für das Gesundheitswesen sind wir in 19 Ländern tätig und beschäftigen über 9.000 engagierte Mitarbeitende. Du wirst in einem dynamischen [...]
MEHR INFOS ZUM STELLENANGEBOT[...] und innovativen Umfeld arbeiten, das voller Möglichkeiten steckt. Mit Deinem Einsatz und Deiner Leidenschaft hast Du die Gelegenheit, [. .. ]

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Job am 11.11.2025 bei JobMESH gefunden CGM Clinical Europe GmbH Technical Writer (m/w/d) • Bayern Erding Abgeschlossenes Studium Deine Aufgabe bei CGM: Als führendes Unternehmen im Bereich Softwarelösungen für das Gesundheitswesen sind wir in 19 Ländern tätig und beschäftigen über 9.000 engagierte Mitarbeitende. Du wirst in einem dynamischen [...]
MEHR INFOS ZUM STELLENANGEBOT[...] und innovativen Umfeld arbeiten, das voller Möglichkeiten steckt. Mit Deinem Einsatz und Deiner Leidenschaft hast Du die Gelegenheit, [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden

Director, Medical Writing, Oncology (1 of 2)

• Basel- Landschaft Führungs-/ Leitungspositionen [. .. ] problems related to the development and implementation of new service offerings and deliverables, working independently to find effective solutions. Write or provide guidance to other writers on [...]
MEHR INFOS ZUM STELLENANGEBOT[...] all types of clinical, regulatory and safety documents, taking a proactive lead in content and scientific strategy with complete independence. Represent the MW department with decisionmaking authority in the R D organization, leading discussions with senior crossfunctional colleagues and external partners to enhance coordination between departments. Directly lead or set objectives for team projects [. .. ] within the Medical Writing (MW) team in close consultation and accordance with the Delivery Unit (DU) . Head in line with R D priorities and TA objectives. Recognized expert medical writer for any document within and across TAs. Accountable for MW resource management and allocation within their portfolio (s) . Can represent MW DU Head or department at highlevel and crossfunctional TA meetings and has significant independent decisionmaking authority. Can step in for DU Head in case of absence. Is a [. .. ]

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Job vor 6 Tagen bei Jobleads gefunden

Global Product Manager Imaging

• Zürich Zuerich [. .. ] value to veterinary customers. This role emphasizes commercial program development, sales training, and portfolio coordination as well as life cycle management. You will be a central link [...]
MEHR INFOS ZUM STELLENANGEBOT[...] between Marketing, Sales, Clinical Education, and Product Development, ensuring consistent execution and growth in this new business segment. Essential Duties And Responsibilities Drive Portfolio Strategy Define clear positioning, messaging, and differentiation for Movoras imaging solutions. Build and maintain a healthy product roadmap that balances commercial needs with technical development (hardware and software) . Enable [. .. ] future needs, and plans accordingly. Execution focus delivers results, keeps projects on track, and ensures teams are aligned. Collaboration works effectively across functions, cultures, and geographies. Communication confident presenter, clear writer, and strong interpersonal skills. Adaptability thrives in a dynamic, fast-growing environment where not everything is predefined. About Movora Movora is the place for leaders with the ambition to shape the future in our field of veterinary Med Tech. With decades of expertise in the advancement of animal health, we [. .. ]

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Job am 06.11.2025 bei Jobleads gefunden

Director Scientific/ Medical Writing

• Mainz, Rheinland- Pfalz Führungs-/ Leitungspositionen [. .. ] concentrates on delivering added value. This includes recruitment, supervision, and development of reports, as well as goal setting, performance assessment, task assignment, and budget. Key responsibilities Responsibilities [...]
MEHR INFOS ZUM STELLENANGEBOT[...] as scientific medical writer including: Write, edit, and format a wide range of documents (of low to high complexity) required for research, non-clinical, clinical development, and post-approval 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 [. .. ]

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Job am 04.11.2025 bei Jobleads gefunden Director Scientific/ Medical Writing • Frankfurt, Hesse Führungs-/ Leitungspositionen [. .. ] Type Full-time Job Function Research, Analyst, and Information Technology Key Responsibilities Write, edit, and format a wide range of documents (of low to high complexity) required for [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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. Coordinate [. .. ] Professional Experience 10 years (handson) experience working in drug development in a therapeutically relevant field, preferably in oncology and/or immunology. 10 years (handson) experience as a scientific or medical writer in the pharmaceutical/ biotech industry. Prior experience drafting documents for multiple indications, preferably in Bio NTechrelevant indications. Prior experience drafting new or updated CTPs and CSRs required for Phase IIII trials. Prior experience drafting highcomplexity variants of IBs, clinical CTDCTAIMPd/IND modules, and clinical CTDBLA/ MAA modules. Prior experience as lead [. .. ]

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Job am 01.11.2025 bei Jobleads gefunden

Medical Writer-Promotional Review

• Hannover, Niedersachsen Senior Scientific Communications Specialist English (Medical Writer/ Promo Review) Location: Fully Remote Europe Essentials Degree: Advanced degree in Pharmacy (Pharm D preferred) , advanced healthcare degree, or equivalent clinical experience. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Experience: 24 years in scientific content creation within the pharmaceutical industry, medical education, or academia. Languages: Fluent in English and German (C1/ C2) . Position Summary The Senior Scientific Communications Specialist provides scientific and medical writing support across multiple therapeutic areas. This role ensures the delivery of accurate, balanced, [. .. ]

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Job am 31.10.2025 bei Jobleads gefunden

Business Development Account Executive (Munich or 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, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job am 09.10.2025 bei Jobleads gefunden

Medical Science Liaison Hematology/ Oncology (m/f/d) - Rheinland-Pfalz, Saarland, Süd-Hessen, . . .

[. .. ] Oncology (m/f/d) Territory: Rheinland-Pfalz, Saarland, Süd-Hessen, Nordwest-Baden-Würtemberg Job Summary Medical Science Liaisons (MSLs) are a team of field-based, highly trained professionals with strong clinical and/or scientific [...]
MEHR INFOS ZUM STELLENANGEBOT[...] backgrounds and excellent communication skills. They represent the Medical Affairs organization to the broad medical/ scientific community. Essential Functions Of The Job (Key Responsibilities) Represent the company and lead medical scientific exchanges within the respective community Develop and lead Key External Experts and investigators engagement plans-identify, [. .. ] Clinician-Southern Germany Austria Head of MSL Innovative Oncology DACH (m/w/d) Associate Director, Field Medical Advisor (m/w/d) Associate Director, Field Medical Advisor (m/w/d) Medical Writer/ Medical Content Manager (m/w/d) Principal Biostatistician (Medical Affairs/ HEOR-EMEA and NA Based) ) Medical Science Liaison-Germany (South) Cologne, North Rhine-Westphalia, Germany 5 days ago Medical Science Liaison Manager-NRW (m/f/d) Medical Science Liaison Oncology South West Germany Medical Science Liaison, Oncology, Germany (m/[. .. ]

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Job am 09.10.2025 bei Jobleads gefunden

Senior Principal Medical Writer-Regulatory-Oncology-Single Sponsor

• Zürich Overview Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address [...]
MEHR INFOS ZUM STELLENANGEBOT[...] modern market realities. Our Clinical Development model centers the customer and the patient, with a focus on simplifying and streamlining work. We collaborate across Functional Service Provider or Full-Service environments to accelerate the delivery of therapies and change lives. WORK [. .. ] considered. This description does not create a contract of employment. The Company complies with applicable equal employment opportunity laws and disability accommodations where required. Headlines and Notes Senior Principal Medical Writer-Regulatory-Oncology-Single Sponsor is the role described. This listing may include additional context from the posting. If you are viewing this externally, verify the posting details with the employer. #J-18808-Ljbffr 65367998 [. .. ]

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Job am 09.10.2025 bei Jobleads gefunden Principal Medical Writer 1, Associate Director • Frankfurt, Hesse Führungs-/ Leitungspositionen Work-Life-Balance Overview ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join [...]
MEHR INFOS ZUM STELLENANGEBOT[...] us on our mission to shape the future of clinical development. We are currently seeking a Principal Medical Writer to join our diverse and dynamic team. As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. Your expertise in medical writing will be crucial in supporting our clients submissions to [. .. ]

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Job am 29.09.2025 bei Jobleads gefunden Lead Medical Writer (m f d) • Bergisch Gladbach, Nordrhein- Westfalen Führungs-/ Leitungspositionen Overview Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for
MEHR INFOS ZUM STELLENANGEBOT[...] class=highlight_text>clinical professionals and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to the market. Job Description As a Medical Writer you are part of our Miltenyi biomedicine business and within the Clinical Development team. You will be responsible for the development and oversight of clinical and regulatory documents that support global drug development programs, including preparation, development, review, revision and finalization of clinical documents for submission to regulatory authorities. Responsibilities [. .. ]

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Job am 16.09.2025 bei Jobleads gefunden Associate Director Scientific/ Medical Writing • Mainz, Rheinland- Pfalz Führungs-/ Leitungspositionen [. .. ] new definition of procedures is required. Key Responsibilities 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, non-clinical, clinical development, and post-approval 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 [. .. ] and oncology. 5 years (handson) experience working in drug development in a therapeutically relevant field, preferably in oncology and/or immunology. 5 years (handson) experience as a scientific or medical writer in the pharmaceutical/ biotech industry. Prior experience drafting documents for multiple indications, preferably in Bio NTechrelevant indications. Prior experience drafting alone new or updated CTPs and CSRs required for Phase IIII trials. Prior experience drafting low to medium complexity variants of the following (new or updated variants) : IBs, clinical CTD modules, [. .. ]

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Job am 05.07.2025 bei Jobleads gefunden Software Medical Device Quality Engineer • Wien [. .. ] edge AI-powered data analysis Services, that make it possible to standardize the process of skin imaging, objectify disease and treatment assessment, and to accelerate data collection and [...]
MEHR INFOS ZUM STELLENANGEBOT[...] analysis in clinical trials and medical routine. We are growing and seeking new, experienced and hands-on team members who think outside of the box, deliver unique ideas and like to work in a fast-paced digital health and medical research environment. You are reliable, ambitious, your heart beats for clinical trials, digital [. .. ] Services Referrals increase your chances of interviewing at SCARLETRED Holding Gmb H by 2x Get notified about new Software Quality Engineer jobs in Vienna, Vienna, Austria. Senior Software Test Engineer Documentation Writer (w/m/d) Software Development Engineer in Test II Software Development Engineer in Test III (All Genders) JAVA Software Engineer-Test Automation (f/m/d) Full Stack Software Engineer-Med Tech Vienna or Remote (EU) Lead Golang Software Engineer, Commercial Systems Were unlocking community knowledge in a new way. Experts [. .. ]

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Neu Job vor 4 Std. bei Neuvoo gefunden Translational Research in Oncology Medical Writer • Berlin Homeoffice möglich Work-Life-Balance Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] bringing the cancer treatments of the future to the patients of today. TRIO is seeking a Medical Writer to join our Medical Writing and Training team. This position reports to the Medical Writing Manager and is home-based in Germany. This position is a fixed-term role starting on March 2, 2026, and ending at the end of August 2026. Responsibilities: Prepare, edit, and finalize trial-related documents, [. .. ]

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Neu Job vor 4 Std. bei Neuvoo gefunden IQVIA Principal Pharmacometrician, FSP • Frankfurt, Hessen [. .. ] and, study phases. Job stability; long-term engagements and development opportunities. Career advancement opportunities. Responsibilities: Contribute to development of protocols, analysis plans, PK/ PD analysis, and pharmacometric reports [...]
MEHR INFOS ZUM STELLENANGEBOT[...] for pre-clinical or Phase I-IV clinical studies. Consult with Clinical Pharmacology staff on study design, analyses, clinical development plans. Plan and execute a wide range of pharmacometric analyses to inform clinical pharmacology and drug development decisions Prepare or review PK/ PD sections of dossiers for product registration and communicate with regulatory [. .. ] and development decisions. Ensure quality and timely delivery of project PK/ PD deliverables. Collaborate in cross functional teams that include Project Manager, CRA, Data Manager, Biostatistician, Programmer, and/or Medical Writer. Maintain awareness of overall developments in the field of pharmacometrics and clinical pharmacology, based on current literature, application of new technology, attendance at professional meetings, etc. Qualifications: Pharm D, Ph. D. (or equivalent) in pharmacology, pharmacy, pharmacometrics, pharmaceutics, biology, mathematics, statistics, engineering, or a field with significant modeling-related content/ training [. .. ]

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Job am 12.11.2025 bei Neuvoo.com gefunden CGM Clinical Europe GmbH Technical Writer (m/w/d) • Sankt Wolfgang Abgeschlossenes Studium Deine Aufgabe bei CGM: Als führendes Unternehmen im Bereich Softwarelösungen für das Gesundheitswesen sind wir in 19 Ländern tätig und beschäftigen über 9.000 engagierte Mitarbeitende. Wir empfehlen allen potenziellen Bewerbern, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] vor der Bewerbung die vollständige Stellenbeschreibung zu lesen. Du wirst in einem dynamischen und innovativen Umfeld ar [. .. ]

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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 Niedersachsen (4 Jobs), Rheinland-Pfalz (3 Jobs) und Bayern (2 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Writer Jobs?

Clinical Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.


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Dauer: 0.0345 s., Vers. V.2025-d-2007-Ind-141