Clinical Scientist
Vor 3 Tagen
For our client in Basel, we are looking for a
**Clinical Scientist**
**Responsibilities**
- The Clinical Scientist will support the overall clinical and scientific activities regarding study planning, preparation, management, evaluation, monitoring, reporting, and documentation
- Gives clinical and scientific input to and reviews clinical regulatory documents (clinical study reports, investigator’s brochure, safety reports, submission to health authorities)
- Assists in and/or may lead part of the development and writing of study related documents
- Assists in the ongoing review of data during study conduct
- May contribute to response to questions from health authorities
- May provide clinical scientific input for final study reports and annual report documentation
- Assists in the management of studies and supports the training and science input to operation colleagues and study site staff
- May support safety representatives in the serious adverse events reporting process and safety evaluation
- Represents clinical science in study management teams
- Ensures GCP compliance in assigned tasks
- Assist in preparing materials for use in internal and external presentations (e.g. advisory board meetings, steering committee meetings, etc.)
**Profile**
- PhD-/MD-/PharmD-level (or equivalent relevant experience)
- 5+ years of experience in clinical drug development
- Previous experience in oncology trials highly desirable
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