9 Jobs für Clinical Research Writer
Stellenangebote Clinical Research Writer Jobs
Neu Job vor 4 Std. bei Jobleads gefunden
• 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 [. .. ] business partners and customers. Creates a positive Credobased work environment for staff members. Shows openness to new ideas and fosters organizational learning. Required Skills : Preferred Skills Business Writing Clinical Research and Regulations Clinical Trials Operations Copy Editing Cross Functional Collaboration Developing Others Inclusive Leadership Industry Analysis Leadership Medical Affairs Medical Communications Performance Measurement Quality Validation Standard Operating Procedure (SOP) Succession Planning Tactical Planning Required Experience Director Key Skills Crisis Management, Marketing, Public Relations, Fundraising, Media Relations, Constant Contact, Strategic Planning, [. .. ]
Job am 06.11.2025 bei Jobleads gefunden
• 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 [. .. ]
Job am 04.11.2025 bei Jobleads gefunden
Director Scientific/ Medical Writing
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] apply for the Director Scientific/ Medical Writing role at Bio NTech SE. Mainz, Germany; London, United Kingdom Full time Job ID: 9928 Seniority Level Director Employment Type [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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 [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
[. .. ] 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 backgrounds [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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, [. .. ] you have any questions or concerns or would like to exercise your rights. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Incyte by 2x Get notified about new Medical Science Liaison jobs in Germany. Medical Science Liaison Oncology North Germany (Senior) Medical Affairs Scientist (m/w/d) Field Specialty Care: Inflammation Immunology, Gebiet: Bayern Medical Affairs 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/[. .. ]
Job am 09.10.2025 bei Jobleads gefunden
• 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 us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
Job am 16.09.2025 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] and/or 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) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] 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, [. .. ]
Job am 05.07.2025 bei Jobleads gefunden
• 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 health and artificial intelligence. You like to prove yourself and like to work in an international team and highly collaborative job environment. Job Brief We are looking for an experiences Software Device Quality Engineer who is who develops [. .. ] 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 [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
Translational Research in Oncology
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to 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, [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
IQVIA
• 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 required Minimum of 3 years experience in Pharmacokinetics or Pharmacology for Clinical Research Organization or pharmaceutical environment Minimum of 2 years in applying model-based methods in pre-clinical and clinical drug development Expert knowledge of pharmacometric concepts, including compartmental and noncompartmental analysis, population PK modeling, current therapeutic environment, and drug development trends. Scientific skills demonstrated in facilitating the (early/ full) clinical development [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Research Writer pro Jahr?
Als Clinical Research Writer verdient man zwischen EUR 40.000,- bis EUR 65.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Research Writer Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 9 offene Stellenanzeigen für Clinical Research Writer Jobs.
In welchen Bundesländern werden die meisten Clinical Research Writer Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Research Writer Jobs werden derzeit in Niedersachsen (3 Jobs), Rheinland-Pfalz (3 Jobs) und Hessen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Research Writer Jobs?
Clinical Research Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
