25 Jobs für Scientific WRITER
Stellenangebote Scientific WRITER Jobs
Job gestern bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] advanced degree in scientific, medical, or clinical discipline (e. g. , Ph D, Pharm D, or equivalent) is required; Ph D preferred Minimum of 810 years of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relevant industry experience as a regulatory/ scientific writer in a pharmaceutical, biotech, or CRO environment CTD experience; vendor oversight a plus Experience authoring clinical study reports, protocols, protocol amendments, and Investigators Brochures Experience authoring briefing books and Module 2 clinical summaries is a plus Solid understanding of drug development, clinical research, data analysis, CTD, ICH guidelines, Gx P, regulatory [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
K- Recruiting Life Sciences
Freelance CMC Regulatory Writer
• Stuttgart, BW
Freiberuflich
Freelance CMC Regulatory
Writer (m/w/D) Aufgaben: Erstellung und Pflege von CMC-relevanten Abschnitten in IMPDs und IND Applications Erstellung regulatorischer Dokumente für klinische Entwicklungsprogramme Phase 13 Vorbereitung von Unterlagen für FDA [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Type B/ C und Pre-IND Meetings Unterstützung bei EMA Scientific Advice Procedures Erstellung von Briefing Books, Meeting Packages, Q A- und Background Documents Aufbereitung komplexer CMC-Inhalte für Behördeninteraktionen Zusammenarbeit mit CMC- und Regulatory-Stakeholdern Qualifikation: Mehrjährige Erfahrung im CMC Regulatory Writing Fundierte Erfahrung mit IMPDs und/oder IND Applications Erfahrung mit FDA- und EMA-Behördeninteraktionen Kenntnisse im Bereich CMC, [. .. ]
Job vor 13 Tagen bei Neuvoo.com gefunden
K- Recruiting Life Sciences
• Baden- Württemberg
Freiberuflich
Freelance CMC Regulatory
Writer (m/w/D) Aufgaben: Erstellung und Pflege von CMC-relevanten Abschnitten in IMPDs und IND Applications Erstellung regulatorischer Dokumente für klinische Entwicklungsprogramme Phase 13 Vorbereitung von Unterlagen für FDA [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Type B/ C und Pre-IND Meetings Unterstützung bei EMA Scientific Advice Procedures Erstellung von Briefing Books, Meeting Packages, Q A- und Background Documents Aufbereitung komplexer CMC-Inhalte für Behördeninteraktionen Zusammenarbeit mit CMC- und Regulatory-Stakeholdern Qualifikation: Mehrjährige Erfahrung im CMC Regulatory Writing Fundierte Erfahrung mit IMPDs und/oder IND Applications Erfahrung mit FDA- und EMA-Behördeninteraktionen Kenntnisse im Bereich CMC, [. .. ]
Job gestern bei Jobleads gefunden
Senior Medical Writer
[. .. ] guidelines Ability to work with company/ client SOPs, standards, templates, authorship requirements, and style/ formatting guides Experience coordinating quality and editorial reviews and managing source documentation Ability [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to peer review scientific content for clarity, consistency, and format Ability to review statistical analysis plans and table/ figure/ listing specifications Clinical literature search skills and knowledge of copyright requirements Ability to provide technical support, training, and consultation Ability to mentor less experienced medical writers Knowledge of industry topics and regulatory requirements affecting medical [. .. ]
Job gestern bei Jobleads gefunden
Technical
Writer Editor II Fully Remote United States Job Type Full-time Description Overview Tanaq Management Services (TMS) delivers professional,
scientific, and technical services and information technology (IT) solutions to federal [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] agencies in the health, agriculture, technology, and other government services. TMS is a subsidiary of the St. George Tanaq Corporation, an Alaskan Native Corporation (ANC) committed to serving Federal customers while also giving back to the Tanaq native community and [. .. ]
Job gestern bei Jobleads gefunden
Medical Writer Oncology Publications
Responsibilities Design, develop, and edit materials for varied audiences, including slide decks, digital materials, manuscripts, congress publications, and meeting materials Deliver high-quality, client-ready first drafts for
scientific review Research content, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure technical accuracy, and critically review and amend work Incorporate feedback accurately and consistently Complete written materials within allocated project timelines Perform data checking in line with BOLD processes Keep abreast of scientific developments and share relevant knowledge with internal teams and clients Work flexibly across client [. .. ]
Job gestern bei Jobleads gefunden
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] process (discovery to market) , biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets. Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection. Advanced applied knowledge of: Documentation required for the conduct of clinical studies Protocol design (including objectives, efficacy and safety endpoints, and procedures for collecting and reporting AEs and SAEs) Study results reporting Integrated results reporting Management Experience: Prior administrative [. .. ]
Job gestern bei Jobleads gefunden
Technical Writer, Editor II
[. .. ] Establish, track, and communicate project milestones from report initiation through final dissemination Monitor workflow using approved job tracking systems and file retention procedures Perform substantive and technical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] editing of complex scientific reports using Microsoft Word, Adobe Acrobat, and Adobe In Copy Provide expertise in style guides and ensure compliance with style guides and plain language standards Review and correct medical and scientific terminology Edit and format narrative text, tables, figures, references, graphics, and supplementary materials Serve as primary liaison between authors [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
[. .. ] and data integrity. Contributes to the development and optimization of Clinical Affairs SOPs. Performs other non-routine duties as assigned. Required Knowledge, Skills and Abilities Bachelors Degree in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a relevant scientific discipline, or equivalent combination of education and experience. A minimum of 3 years medical writing experience. Direct experience working on clinical evaluations within the Medical Device industry a plus. Medical writing certification a plus. A high level attention to detail and the ability to own and drive accuracy. Strong interpersonal [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Scientific Director-Medical Communications
Führungs-/ Leitungspositionen
[. .. ] disability, long term health condition, or are neurodiverse. If youd like to apply and need adjustments made, you can let us know in your application. About the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role As a Scientific Director you will be a scientific expert, providing insights and knowledge to projects, clients and new business efforts. You will review projects for strategic alignment and scientific accuracy, and when needed, act as the medical writer for more scientifically complex projects. Acting as a client relationship manager, you will build scientific credibility and partnerships, ensuring a high level of service with each client. You will provide scientific and strategic expertise to new business development activities, researching and developing content for pitches, as well as being part [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• München, Bayern
Medical
Writer/ Senior Medical Writer (German/ English Medical Affairs Marketing) At Real Chemistry, making the world a healthier place isnt just an aspirationits our everyday reality. Our drive to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] transform healthcare is informed by our blend of deep scientific expertise, human-centred creativity, and AI-driven insights, fostering a unique environment where innovation thrives and our people are impact-obsessed. As a global agency, we provide a full suite of services across healthcare communications and marketing to our clients, including top players in the pharmaceutical and biotech industries. Our [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Technical Writer-Editor
[. .. ] and Plant Health Inspection Service (APHIS) ; Plant Protection and Quarantine (PPQ) . You will design, develop, produce and maintain operational and policy manuals, job aids, training [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] materials, and other scientific and technical communication. Major Duties The duties described are for the full-performance level. At developmental grade levels, assignments will be of more limited scope, performed with less independence and limited complexity. The duties may include, but are not limited to: Identifies and develops technical, policy, scientific, and procedural manuals [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
• 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 modules2.4 and2.5. In doing so, you respond to deficiency letters during registration procedures [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Senior Medical Writer Promotional Medical Writing
[. .. ] experience in the medical communication, pharmaceutical and/or healthcare industry Command of American Medical Association (AMA) style Strong proficiency in Microsoft Word, Microsoft Power Point, and Adobe Acrobat [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Familiarity with scientific search engines including Pub Med and Google Scholar Strong written and verbal communication High analytical ability Ability to prioritize deadline-sensitive projects and juggle competing client priorities Team-and detail-oriented Core Competencies Demonstrates expertise in developing high-quality, medically accurate content for medical communication resources, with a strong command [. .. ]
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 contributing to dossier strategies and writing the dossier modules, preparing submissions using tools such as our proprieteary EPRI, and actively participating in strategic projects, risk assessments, [. .. ]
Job am 01.09.2026 bei Jobleads gefunden
Medical Writer/ Senior Medical Writer (German/ English Medical Affairs Marketing)
At Real Chemistry, making the world a healthier place isnt just an aspirationits our everyday reality. Our drive to transform healthcare is informed by our blend of deep
scientific [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise, human-centred creativity, and AI-driven insights, fostering a unique environment where innovation thrives and our people are impact-obsessed. As a global agency, we provide a full suite of services across healthcare communications and marketing to our clients, including top players in the pharmaceutical and biotech industries. Our [. .. ] for healthcare and connection, we invite you to explore our opportunities. Discover your purpose. Embrace innovation. Experience #Lifeat Real Chem. What is the role? Were looking for a Medical Writer/ Senior Medical Writer to join our team at Real Chemistry Germany. You will be the first hire in our German-based content team, and will be responsible for developing materials across medical affairs and marketing projects in a range of therapy areas for top pharma clients. As this role will [. .. ]
Job am 31.08.2026 bei Jobleads gefunden
• München, Bayern
Medical
Writer/ Senior Medical Writer (German/ English Medical Affairs Marketing) At Real Chemistry, making the world a healthier place isnt just an aspirationits our everyday reality. Our drive to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] transform healthcare is informed by our blend of deep scientific expertise, human-centred creativity, and AI-driven insights, fostering a unique environment where innovation thrives and our people are impact-obsessed. As a global agency, we provide a full suite of services across healthcare communications and marketing to our clients, including top players in the pharmaceutical and biotech industries. Our [. .. ]
Job am 21.08.2026 bei Jobleads gefunden
Director, Principal Medical Writer, Europe
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] will report to the VP, Regulatory Affairs, Europe. Primary Responsibilities: Author, edit and coordinate high-quality clinical regulatory documents, including: Responses to Health Authority questions (EMA, MHRA, Swissmedic, etc) . Scientific Advice briefing books and meeting packages. Risk Management Plan (RMP) . Periodic safety documents (as applicable) . As needed, serve as a medical writing lead for complex clinical regulatory documents, supporting clinical development including protocols, IBs, CSRs, and CTA modules. Other regulatory documents supporting lifecycle management, variations and renewals. Coordinate [. .. ]
Job am 21.08.2026 bei Jobleads gefunden
• 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 with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 01751623 [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Medical Writer
[. .. ] powered advice on this job and more exclusive features. Direct message the job poster from Life Sciences Recruitment Senior Consultant Experienced Traveller Ex Professional Golfer Average Footballer [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Job Title: Medical Writer Promotional Materials (Remote, Germany) Are you a talented Medical Writer with a passion for crafting compelling, scientifically accurate promotional content? Join a leading Medical Communications agency and help shape impactful materials for top healthcare and pharmaceutical clients. About the Role As a Medical Writer, youll focus on developing high-quality [. .. ] therapeutic area trends and medical advancements About You Experience in Medical Writing, preferably within Med Comms or Pharma Strong knowledge of promotional materials and regulatory requirements Ability to translate complex scientific data into clear, compelling narratives Excellent attention to detail and ability to work in a fast-paced environment Fluent in English and German Whats in it for You? Fully remote role work from anywhere in Germany Competitive salary benefits package Opportunity to work with leading global pharma brands Career development [. .. ]
Job am 18.08.2026 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 [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Medical Writer
• Hannover, Niedersachsen
[. .. ] participating in oral hearings with relevant authorities. Independently prepare benefit assessment dossiers for pharmaceuticals within the AMNOG process and for EU Health Technology Assessments (HTA) in collaboration [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with clients. Perform scientific and statistical analysis, interpretation, gap analysis, 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) [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Senior Frontend Engineer-React
• Berlin
[. .. ] about the power of millions of scientists working together to tackle them. We provide scientists with the help and support they need by connecting them to the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] worlds most active scientific community. Weve built a platform that gives the worlds scientists the tools and services they need to connect, collaborate, and advance their research. Over 25 million members from 193 countries use Research Gate to share, discover, and discuss research. Objective of the role Were looking for an enthusiastic frontend engineer [. .. ] to connect with existing and future authors. Your immediate colleagues will consist of Java Script and PHP engineers, an Engineering Manager, a Product Manager, a UX Designer, and a UX Writer. Our team places great value on our collaborative and communicative work culture and we eagerly anticipate integrating a new Engineer into this environment. Responsibilites Create web interfaces using Type Script and React for new products and features. Seamlessly integrate our front-end with our back-end world using Graph QL and [. .. ]
Job am 18.08.2026 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 vor 13 Tagen bei Neuvoo.com gefunden
K- Recruiting Life Sciences
Freelance CMC Regulatory Writer
Freiberuflich
Freelance CMC Regulatory
Writer (m/w/D) Aufgaben: Erstellung und Pflege von CMC-relevanten Abschnitten in IMPDs und IND Applications Erstellung regulatorischer Dokumente für klinische Entwicklungsprogramme Phase 13 Vorbereitung von Unterlagen für [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] FDA Type B/ C und Pre-IND Meetings Unterstützung bei EMA Scientific Advice Procedures Erstellung von Briefing Books, Meeting Packages, Q A- und Background Documents Aufbereitung komplexer CMC-Inhalte für Behördeninteraktionen Zusammenarbeit mit CMC- und Regulatory-Stakeholdern Qualifikation: Mehrjährige Erfahrung im CMC Regulatory Writing Fundierte Erfahrung mit IMPDs und/oder IND Applications Erfahrung mit FDA- und EMA-Behördeninteraktionen Kenntnisse im Bereich CMC, [. .. ]
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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 25 offene Stellenanzeigen für Scientific WRITER Jobs.
In welchen Bundesländern werden die meisten Scientific WRITER Jobs angeboten?
Die meisten Stellenanzeigen für Scientific WRITER Jobs werden derzeit in Niedersachsen (3 Jobs), Bayern (3 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Scientific WRITER Jobs?
Scientific WRITER Jobs gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.
