Clinical/Medical Scientist
Clinical/Medical Scientist
Clinical/Medical Scientist
Clinical/Medical Scientist
headcount
Pharma, Medizintechnik
Basel
- Art der Beschäftigung: Vollzeit
- Vor Ort
- Zu den Ersten gehören

Clinical/Medical Scientist
Über diesen Job
Start: ASAP
We are supporting a pharma company in Basel that is looking for a Clinical / Medical Scientist to join their team on a 12 month contract. This role will focus on supporting clinical trial execution, medical monitoring, and cross-functional collaboration across ongoing clinical programs.
This position is ideal for someone with strong clinical development experience who enjoys working in a collaborative, outsourced CRO model and can contribute both scientifically and operationally.
Responsibilities
- Draft key clinical trial and program-level documents in collaboration with Clinical Operations, Biostatistics, Medical Writing and CRO partners
- Support clinical aspects of study startup, execution and close-out in close collaboration with Clinical Operations, Data Management and CROs
- Contribute to medical monitoring of efficacy and safety data from clinical trials
- Act as a point of contact for investigational sites to ensure smooth study conduct
- Support the development and execution of the Data Review Plan
- Contribute to the analysis and drafting of clinical trial reports and scientific publications
- Support planning, conduct and follow-up of external clinical development and study-related meetings
- Maintain clinical aspects of the Trial Master File
- Provide operational support to the Clinical Development team including meeting coordination, inspection readiness and general organization
Requirements
- Bachelor’s or advanced degree in a scientific discipline, or Medical Degree
- 5+ years of experience in the pharmaceutical industry, including at least 3 years within Clinical Development teams
- Experience managing clinical trials within multidisciplinary teams
- Experience working in fully outsourced CRO models
- Strong medical and scientific expertise relevant to clinical programs
- Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes and clinical development
- Excellent scientific writing skills
- Strong understanding of statistical analysis methods with the ability to interpret and communicate data clearly
- In-depth knowledge of drug development processes
Unternehmens-Details

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Personaldienstleistungen und -beratung