19 Jobs für Scientific WRITER
Stellenangebote Scientific WRITER Jobs
Job am 09.03.2026 bei Jobleads gefunden
• Freiburg im Breisgau, Baden- Württemberg
[. .. ] as 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: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Global 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 [. .. ]
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
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] data or other scientific content into a logical, scientifically balanced compelling medical narrative for the appropriate audience. Your tasks: Planning, writing, reviewing and submitting manuscripts on clinical drug trials in humans for peer-reviewed journals and abstracts for scientific conferences Data visualization of data from clinical drug trials Supporting preparation of posters and conference [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen Homeoffice möglich
Head of Communications (all genders) 80 SLSP AG-Zurich Join us in shaping the future of
scientific information in Switzerland The Swiss Library Service Platform (SLSP) headquartered in Zurich is a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service provider for libraries and collaborates with them to run the national library platform swisscovery that gathers scientific information from 500 libraries in Switzerland and makes it easily accessible and simple to find. At SLSP, you [. .. ] ideally in a similar environment. You are familiar with the Swiss library and/or university landscape or you are willing to quickly familiarise yourself with it. You are a confident writer with excellent editorial skills and the ability to tailor your writing to specific target groups. You can navigate digital communication channels with ease and understand reach, positioning and marketing logic. You have an affinity for digitalisation, AIbased tools and modern communication formats. You have proven experience in managing multilayered stakeholder [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Halle (Saale) , Sachsen- Anhalt
Abgeschlossenes Studium
Vertragsart: Unbefristete Direktanstellung Wir unterstützen ein international tätiges Unternehmen aus den Bereichen Life Sciences, personalisierter Medizin und molekularer Diagnostik bei der Besetzung einer Position als Medical
Writer (m/w/d) . Das [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Unternehmen entwickelt und vertreibt innovative diagnostische Lösungen mit starkem wissenschaftlichem Fokus, insbesondere in der Onkologie und der molekularen Medizin. Ihre Aufgaben Erstellung hochwertiger medizinischer und wissenschaftlicher Inhalte (Medical Scientific Writing) für digitale und gedruckte Medien Verfassen von Scientific Content in Deutsch und Englisch Entwicklung von Fachartikeln, Whitepapers, Präsentationen und edukativen Materialien Übersetzung komplexer wissenschaftlicher, laborbasierter und diagnostischer Daten in verständliche Inhalte für unterschiedliche Zielgruppen Unterstützung der Medical Communication sowie marketingnaher Inhalte mit wissenschaftlichem Anspruch Sicherstellung der Einhaltung regulatorischer, wissenschaftlicher [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] Writing (MW) process working groups or Communities of Practice. Writes or coordinates all types of clinical and regulatory documents, taking a proactive or lead role in terms of content and scientific strategy. Establishes and drives document timelines and strategies independently. Guides or trains cross-functional team members on processes and best practices; coaches or mentors more junior writers. Proactively identifies and champions departmental process improvements. May develop and present best practices or innovations to internal or external audiences. May lead cross-[. .. ]
Job am 09.03.2026 bei Jobleads gefunden
A leading healthcare consultancy is seeking an Experienced Medical
Writer for the Regulatory Affairs team in Austria. The successful candidate will develop and review high-quality regulatory documents, ensuring
scientific accuracy [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and strategic alignment. Required qualifications include a Ph D in Life Sciences or MD and at least 3 years of related experience. This role offers the chance to engage with clients and contribute to important healthcare projects while working in a flexible and dynamic environment. #J-18808-Ljbffr 83447542 [. .. ]
Job am 09.03.2026 bei Jobleads gefunden
Experienced Medical
Writer Regulatory Affairs Austria Location: Austria We are looking for a highly motivated and experienced Medical Writer to join a dynamic Regulatory Affairs team. In this role, you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] will lead the development and review of high-quality, evidence-based regulatory documents supporting a wide range of projects. You will work closely with clients and internal teams to ensure scientific accuracy, clarity, and strategic alignment of content for submissions such as CTDs, briefing books, and other regulatory materials. Key Responsibilities Lead preparation and review of regulatory and scientific documents across multiple projects Collaborate and communicate with clients on assigned deliverables Write and refine compelling, evidence-based regulatory and medical 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] Writing (MW) process working groups or Communities of Practice. Writes or coordinates all types of clinical and regulatory documents, taking a proactive or lead role in terms of content and scientific strategy. Establishes and drives document timelines and strategies independently. Guides or trains cross-functional team members on processes and best practices; coaches or mentors more junior writers. Proactively identifies and champions departmental process improvements. May develop and present best practices or innovations to internal or external audiences. May lead cross-[. .. ]
Job am 04.03.2026 bei Jobleads gefunden
[. .. ] drive traffic (keyword research) , with compelling copy, encouraging a desired action, is a distinct advantage. Passion for networking and stakeholder engagement. Being up to date with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the latest technical/ scientific developments and relating them to various projects. Client-oriented attitude with focus on creating strong long-term relationships with clients and encouraging others to work toward this goal. Ability to assure timely completion of assignments. Skilled in problem identification and problem solving. Detail oriented, well organized and timeline driven with [. .. ]
Job am 22.02.2026 bei Jobleads gefunden
Senior Medical Writer
• Berlin
[. .. ] empowered to find creative solutions and make a meaningful impact on clinical development across rare disease, oncology, neurology, immunology and inflammation. About the Role We are seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Medical Writer to join our Medical Writing and Pharmacovigilance Team and take ownership of clinical, regulatory and safety writing projects. This is a fulltime, hybrid role reporting to the Head of Medical Writing and Pharmacovigilance, with one to two days per week based in our Berlin office. Key Responsibilities Prepare a wide [. .. ] safety reports and Risk Management Plans. Collaborate closely with crossfunctional teams, including pharmacovigilance, regulatory affairs and clinical development, to ensure documents are accurate and submissionready. Review complex documents for consistency, scientific accuracy and alignment with client standards and regulatory requirements (e. g. , ICH, GVP, MDR) . Manage review cycles and project timelines in coordination with clients and internal stakeholders to meet delivery milestones. Act as a subject matter advisor on medical writing and regulatory documentation for clients and internal teams. [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] delivering medicines/ therapies to a broad market across various therapeutic areas. Extensive experience in writing HTA dossiers, eg AMNOG, HAS, NICE, CDA dossier preferred. Bachelors Degree or higher in a scientific discipline. Outstanding written and oral communication 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 [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
Senior Project Education Manager
• Berlin
Abgeschlossenes Studium
[. .. ] wissenschaftlicher Themen in effektive Lernkonzepte und Curricula Beratung zu didaktischer Struktur, Lernzielen und Umsetzung in digitalen Formaten Sicherstellung von Qualität, Konsistenz und Relevanz der Inhalte Enge Abstimmung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] mit Ärzt:innen, Medical Writer:innen und Designer:innen Prozessmanagement Optimierung Weiterentwicklung und Standardisierung unserer Abläufe im Projekt- und Content-Management Einführung effizienter Tools und Workflows (z. B. KI-basierte Prozesse) Monitoring von Timelines, Budgets und Qualitätskennzahlen Strategische Weiterentwicklung Identifikation neuer Themen und Formate in Zusammenarbeit mit Partnern Unterstützung bei der Angebotsentwicklung und strategischen Planung neuer Medical [. .. ] Beobachtung medizinischer Trends und regulatorischer Entwicklungen Ihr Profil Abgeschlossenes Studium in Medizin, Pharmazie, Biologie, Public Health, Medical Education oder einem verwandten Bereich Mehrjährige Erfahrung im Projektmanagement im Bereich Medical Education, Scientific Communication oder Healthcare-Agentur Fähigkeit, medizinische Inhalte und Lernziele zu verstehen und didaktisch sinnvoll zu strukturieren Erfahrung in der Zusammenarbeit mit Pharmaunternehmen und medizinischen Expert:innen Strukturierte, lösungsorientierte Arbeitsweise und Freude an Organisation und Abstimmung Sicherer Umgang mit Projektmanagement-Tools (Asana) Interesse an digitalen Lernformaten und KI-gestützten Workflows Sehr gute [. .. ]
Job am 12.11.2025 bei Jobleads gefunden
MEDICAL WRITER (f/m/d)
• München, Bayern
[. .. ] media posts, etc. ) - Strategic idea development storytelling at the interface of medical and marketing-Target group-oriented preparation of content (HCPs vs. patients) Quality control referencing: Ensuring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the scientific accuracy of medical content, documentation in release systems (e. g. Veeva) Familiarization with various indications: Research analysis of medical studies Mediation of medical content: Internal training clear explanation of complex medical topics for our project management and creative team This is what we want from you Professional experience in science [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
Excelya
Freelancer Senior Medical Writer (medical devices)
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
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 of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the clinical writing process. Provides HTA writing expertise for multiple compounds and/or projects, expertise in HTA, oncology is a plus within a therapeutic [. .. ] delivering medicines/ therapies to a broad market across various therapeutic areas. Extensive experience in writing HTA dossiers, eg AMNOG, HAS, NICE, CDA dossier preferred. Bachelors Degree or higher in a scientific discipline. Outstanding written and oral communication 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 [. .. ]
Job vor 14 Tagen bei Neuvoo gefunden
Veristat
Principal Medical Writer
Job Description : Principal Medical
Writer The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory guidelines, and individual company document standards. The Principal Medical Writer works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams. Make an Impact at Veristat Join a [. .. ]
Job am 27.02.2026 bei Neuvoo gefunden
HELM AG
(Senior) Clinical Trial Manager (m/f/d)
• Hamburg
[. .. ] our team in the Finished Dosage Form Programs we are looking for a Manager Clinical Development (m/f/d) with a clinical life science background. In this position, you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 offers you the opportunity to actively influence clinical development decisions and create real value for customers. [. .. ] 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 [. .. ]
Job am 26.02.2026 bei Neuvoo gefunden
Veristat
Senior Medical Writer
Job Description : Senior Medical
Writer The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory guidelines, and individual company document standards. The Senior Medical Writer works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams. Make an Impact at Veristat Join a [. .. ]
Job am 12.02.2026 bei Neuvoo gefunden
HELM AG
(Senior) Manager Clinical Development (m/w/d)
• Hamburg
[. .. ] klinische und/oder präklinische Studien gemäß regulatorischen Vorgaben und verantworten das Qualitätsmanagement des gesamten Studienprogramms. Dazu gehört auch die Beratung sowie Konzeption von Studieninhalten mit Behörden sowie die [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Erstellung von Scientific-Advice-Unterlagen. Ein weiterer Bestandteil Ihrer Rolle umfasst Tätigkeiten als Medical Writer : Sie erstellen und prüfen wissenschaftliche Dokumente zur Wirksamkeit und Sicherheit unserer Produkte. Dabei stellen Sie die fristgerechte Erstellung nichtklinischer und klinischer Dokumentationen für Zulassungseinreichungen sicher, einschließlich der Beauftragung und Prüfung der Module 2.4 und 2.5. Hierbei bearbeiten Sie außerdem Mängelschreiben im Rahmen von Registrierungsverfahren und managen entsprechende [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Scientific WRITER pro Jahr?
Als Scientific WRITER verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Scientific WRITER Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 19 offene Stellenanzeigen für Scientific WRITER Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Scientific WRITER Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Scientific WRITER Jobs.
Welche Unternehmen suchen nach Bewerbern für Scientific WRITER Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Scientific WRITER Stellenangebote:
- Veristat (2 Jobs)
- HELM AG (2 Jobs)
- Excelya (1 Job)
- Abb Vie (1 Job)
- Dr. Falk Pharma GmbH (1 Job)
In welchen Bundesländern werden die meisten Scientific WRITER Jobs angeboten?
Die meisten Stellenanzeigen für Scientific WRITER Jobs werden derzeit in Niedersachsen (3 Jobs), Berlin (2 Jobs) und Hessen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Scientific WRITER Jobs?
Scientific WRITER Jobs gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.
