17 Jobs für Scientific WRITER
Stellenangebote Scientific WRITER Jobs
Job vor 2 Tagen bei StepStone gefunden
Kintiga
• Hannover
Homeoffice möglich
Are you looking for a full-time position in a pan-European strategic consultancy as a Senior Medical
Writer to streamline patient access to life-changing treatments through expert guidance, innovative tools, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] impeccable delivery? Location: Hybrid with office in Hannover regular in-person presence Salary: Competitive, based on experience We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC) , a pan-European specialist consultancy that partners with [. .. ] functional workstreams Develop and execute medical and market access strategies, including HTA dossier strategy, market access risk assessments, and strategic positioning for price negotiations Lead G-BA advice meetings, Joint Scientific Consultations (JSC) , and the development, preparation, and submission of AMNOG and JCA dossiers in close collaboration with clients Collaborate in and promote interdisciplinary, agile teams, applying modern working methods and driving continuous improvement Support business development activities, including proposal development and opportunity identification Actively contribute to knowledge sharing, internal [. .. ]
Job am 03.06.2026 bei XING gefunden
Cactus Life Sciences
• 6000 Luzern
30+ Urlaubstage
[. .. ] Poster, Materialien für Kongresse und Tagungen sowie Literaturrecherchen und -reviews entsprechend den Anforderungen des Kunden und der Zielgruppe mit ausgeprägter Detailgenauigkeit Aktive Mitwirkung bei der Überprüfung von [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Materialien, die von Scientific Writern entwickelt wurden, um die strategische Ausrichtung und wissenschaftliche Genauigkeit sicherzustellen. Bereitstellung von klarem, konstruktivem Feedback Aufbau eines tiefgehenden Verständnisses der betreuten Produkte und Accounts zur Ermöglichung sinnvoller Interaktionen mit Kund:innen und externen Autor:innen, einschließlich beratender Tätigkeiten bei Bedarf Aufbau und Pflege langjähriger Beziehungen zu internationalen Pharmakunden, medizinischen Fachkräften und [. .. ] auf muttersprachlichem oder nahezu muttersprachlichem Niveau, sowie ausgeprägte wissenschaftliche Schreibkompetenz. Promotion in Medizin, Life Sciences, Gesundheitswissenschaften oder Pharmazie oder Master-Abschluss in Life Sciences. Mindestens 3 Jahre Erfahrung als Medical Writer in der pharmazeutischen Industrie, idealerweise in einer Agentur für medizinische Kommunikation. Klarer, prägnanter, wissenschaftlicher Schreibstil mit einem hohen Maß an Detailgenauigkeit und ausgezeichneten Sprachkenntnissen. Erfahrung in Literaturrecherche und -bewertung. Fähigkeit, den Schreibstil flexibel an unterschiedliche Materialien und Zielgruppen anzupassen. Grundkenntnisse in Biostatistik. Fähigkeit zu Multitasking und zur Arbeit unter Zeitdruck. [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Basel- Stadt
[. .. ] quality systems and supply chain distribution knowledge to provide guidance and maintain oversight over complex Gx P processes. The perfect candidate An exceptional candidate holds a Bachelors [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] degree in a relevant scientific or technical field and brings a minimum of three years of comprehensive Quality Assurance experience deeply rooted in a regulated GMP/ GDP environment. They are completely fluent in English (with German being a strong asset) , allowing them to confidently author Master Quality Agreements, manage clinical trial complaint systems, and [. .. ] . 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
[. .. ] Chain Management Distribution (PTDS-L) . They drive continuous improvement and ensure adherence to international GMP/ GDP standards. Perfect Candidate An exceptional candidate holds a Bachelors degree in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a relevant scientific or technical field and brings a minimum of three years of comprehensive Quality Assurance experience deeply rooted in a regulated GMP/ GDP environment. They are completely fluent in English (with German being a strong asset) , allowing them to confidently author Master Quality Agreements, manage clinical trial complaint systems, and [. .. ] 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
[. .. ] quality systems and supply chain distribution knowledge to provide guidance and maintain oversight over complex Gx P processes. The perfect candidate: An exceptional candidate holds a Bachelors [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] degree in a relevant scientific or technical field and brings a minimum of three years of comprehensive Quality Assurance experience deeply rooted in a regulated GMP/ GDP environment. They are completely fluent in English (with German being a strong asset) , allowing them to confidently author Master Quality Agreements, manage clinical trial complaint systems, and [. .. ] . 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 vor 13 Tagen bei Jobleads gefunden
• 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 02.06.2026 bei Jobleads gefunden
• 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 [. .. ]
Job am 24.05.2026 bei Jobleads gefunden
• Berlin
Teilzeit
[. .. ] 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, every financial model, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 pioneered tabular foundation models and are [. .. ]
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 lifecycle: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Evaluation Reports (CERs) , Clinical Evaluation Plans (CEPs) , PMCF plans and reports, State of the Art (SOTA) reports, and PSURs. This is [. .. ] be successful: Strong clinical writing foundation: Handson experience authoring CERs, CEPs, PMCFs, or SOTAs under MDR/ IVDR. Comfortable moving across device categories and therapeutic areas rather than specialising in one. Scientific rigour: You read clinical literature critically, appraise study quality, and can defend your conclusions with evidence, both on the page and in conversation. Customer orientation: You communicate complex clinical content clearly and confidently to diverse audiences, from QA managers to Clevel stakeholders. You take ownership of customer relationships and follow [. .. ]
Job am 12.05.2026 bei Jobleads gefunden
• Baden- Württemberg
[. .. ] and aligned with EU MDR and FDA requirements. The position works closely with Regulatory Affairs, Quality Management, Clinical Affairs, and Development teams and will support activities including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] IFUs, technical files, scientific documentation, audits, and regulatory projects such as MDR transitions and change control activities. Key requirements Experience in writing technical documentation within medical devices or regulated healthcare environments Knowledge of MDR, IVDR, ISO 13485, and/or FDA regulatory requirements Experience preparing technical documentation, IFUs, or regulatory product documentation Ability to communicate [. .. ]
Job am 12.05.2026 bei Jobleads gefunden
Senior Medical Writer
• Hannover, Niedersachsen
[. .. ] health technology developers through the complex journey to achieve successful market access across Europe, with our tailored approach, global perspective and local expertise. WHAT WERE LOOKING FOR [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As Senior Medical Writer at Kintiga, you will take on a leading role in the content and organizational delivery of market access projects. You will act as a key contact for clients, manage timelines and resources, and contribute to the strategic direction and quality of projects. In addition, you will support team development through [. .. ] and crossfunctional workstreams Develop and execute medical and market access strategies, including HTA dossier strategy, market access risk assessments, and strategic positioning for price negotiations Lead GBA advice meetings, Joint Scientific Consultations (JSC) , and the development, preparation, and submission of AMNOG and JCA dossiers in close collaboration with clients Collaborate in and promote interdisciplinary, agile teams, applying modern working methods and driving continuous improvement Support business development activities, including proposal development and opportunity identification Actively contribute to knowledge sharing, internal [. .. ]
Job am 27.03.2026 bei Jobleads gefunden
Associate Director Scientific/ Medical Writing
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Mainz, Germany full time Job ID: 11231 About the Role As an Associate Director
Scientific/ Medical Writing, you will play a pivotal role in advancing Bio NTechs mission to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] revolutionize medicine by ensuring the timely creation of highquality scientific and regulatory documents. Your contributions will directly impact the development and approval of novel therapeutic agents, supporting Bio NTechs efforts to address diseases with high medical needs. Collaborating [. .. ] 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 04.03.2026 bei Jobleads gefunden
Medical Writer
[. .. ] 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 [. .. ]
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 [. .. ]
Job vor 2 Tagen bei Neuvoo.com gefunden
Cactus Life Sciences
Senior Medical Writer
• Berlin
[. .. ] Poster, Materialien für Kongresse und Tagungen sowie Literaturrecherchen und -reviews entsprechend den Anforderungen des Kunden und der Zielgruppe mit ausgeprägter Detailgenauigkeit. Aktive Mitwirkung bei der Überprüfung von [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Materialien, die von Scientific Writern entwickelt wurden, um die strategische Ausrichtung und wissenschaftliche Genauigkeit sicherzustellen. Bereitstellung von klarem, konstruktivem Feedback. Aufbau eines tiefgehenden Verständnisses der betreuten Produkte und Accounts zur Ermöglichung sinnvoller Interaktionen mit Kund:innen und externen Autor:innen, einschließlich beratender Tätigkeiten bei Bedarf. Aufbau und Pflege langjähriger Beziehungen zu internationalen Pharmakunden, medizinischen Fachkräften und [. .. ] auf muttersprachlichem oder nahezu muttersprachlichem Niveau, sowie ausgeprägte wissenschaftliche Schreibkompetenz. Promotion in Medizin, Life Sciences, Gesundheitswissenschaften oder Pharmazie oder Master-Abschluss in Life Sciences. Mindestens 3 Jahre Erfahrung als Medical Writer in der pharmazeutischen Industrie, idealerweise in einer Agentur für medizinische Kommunikation. Klarer, prägnanter, wissenschaftlicher Schreibstil mit einem hohen Maß an Detailgenauigkeit und ausgezeichneten Sprachkenntnissen. Erfahrung in Literaturrecherche und -bewertung. Fähigkeit, den Schreibstil flexibel an unterschiedliche Materialien und Zielgruppen anzupassen. Grundkenntnisse in Biostatistik. Fähigkeit zu Multitasking und zur Arbeit unter Zeitdruck. [. .. ]
Job am 15.04.2026 bei Neuvoo gefunden
Ashfield
Scientific Manager/ Medical Writer
• Mannheim, Baden- Württemberg
Fürunseren Standortin Mannheim suchenwirqualifizierte Mitarbeiter Innenals
Scientific Manager/ Medical
Writer Medizinische Fortbildung ++ Wissenschaftliche Kommunikation ++ Strategische Beratung IHRE AUFGABEN Mitwirkung an der Entwicklung medizinischwissenschaftlicher Inhalte für Projekte, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] von begutachteter Fachliteratur bis hin zu medizinischwissenschaftlichen Fortbildungsveranstaltungen in einem dynamischen Team Durchführung hochwertiger wissenschaftlicher Analysen, schriftlicher Arbeiten, kreativer Präsentationen und strategischer Beratungsleistungen, die Ziele und Zeitvorgaben von Kunden erfüllen Unterstützung bei [. .. ]
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 [. .. ]
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 17 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:
- Cactus Life Sciences (2 Jobs)
- Kintiga (1 Job)
- Excelya (1 Job)
- Ashfield (1 Job)
- HELM AG (1 Job)
In welchen Bundesländern werden die meisten Scientific WRITER Jobs angeboten?
Die meisten Stellenanzeigen für Scientific WRITER Jobs werden derzeit in Niedersachsen (4 Jobs), Berlin (4 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Scientific WRITER Jobs?
Scientific WRITER Jobs gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.
