Clinical/Medical Scientist
(m/f/d)
Freelance/temporary employment for a project Basel Stadt Start date: asap Reference number: 871198/1
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Responsibilities
1. Draft and review key clinical trial and program-level documents in close collaboration with Clinical Operations, Biostatistics, Medical Writing, and CRO partners
2. Oversee clinical aspects of study start-up, execution, and close-out, working closely with Clinical Operations, Data Management, and CROs
3. Support medical monitoring of efficacy and safety data, contributing to timely issue identification and resolution
4. Serve as a direct clinical contact for investigational sites, ensuring smooth trial conduct across start-up, execution, and close-out phases
5. Own the clinical components of the Data Review Plan and Trial Master File (TMF), ensuring completeness, quality, and inspection readiness
6. Support analysis, interpretation, and dissemination of clinical trial data, including scientific publications, investigator meetings, and clinical development team operations
Profile
7. Bachelor’s degree or advanced degree in a scientific discipline or Medical Degree
8. Experience in the pharmaceutical industry, including multiple years in Clinical Development, with responsibility for multiple clinical trials
9. Proven experience working in fully outsourced CRO models and leading multidisciplinary trial teams
10. Strong medical and scientific expertise relevant to the clinical program, with the ability to build effective partnerships with investigators
11. Thorough knowledge of GCP, clinical trial design, statistics, regulatory requirements, and the overall clinical development process
12. Excellent scientific writing and communication skills, with the ability to interpret data, identify trends, and clearly present trial- or program-level results
Benefits
13. Challenging and varied assignments in a promising and innovative industry
14. Longterm project