Junior Project Associate Science & Medical Affairs
Stratpharma
- Bâle
- Fr. 70'000 par an
- CDI
- Temps-plein
- QA Support :
- Environmental scanning. Following internal and ISO SOPs to maintain the PMS obligations of the company
- Assisting in the preparation of Clinical evaluation reports
- Assisting in the preparation of NPD documental process and record keeping
- Regulatory Support
- Product dossier inputs from Clinical results
- Document preparation and assistance
- Stratpharma QMS system support (review, process management analysis and assistance for QARA team)
- Clinical Plan responsibilities:
- Development of clinical documentation (protocol, case report forms, reports)
- Preparing manuscripts
- Marketing cooperation (NPD and existing products):
- Literature review
- Indication analysis, competitive overview, segmentation
- Pricing analysis, reimbursement landscape
- Market Access responsibilities:
- Preparing submission dossiers
- Compiling clinical and scientific information
- 1 years’ experience in the areas of clinical research preferably in the medical device or pharmaceutical industry.
- New product development experience desirable
- Clinical trial management experience desirable
- Statistical Analysis experience desirable
- Medical Writing/Scientific Writing experience desirable
- Fluent English essential