Experienced Scientific Affairs Associate involved in the preparation of clinical research and regulatory documents, clinical trials documentation with a strong publication record of >25 scientific peer-reviewed papers and conferences presentations. Medical device expert with an aptitude to combine, analyze and present data clearly and concisely.
Communicate scientific input liaising between clinicians and data scientists, encouraging teamwork and colleague interaction as well as working independently.
medical device
writing and editing scientific, medical, regulatory and technical documents
organizational skills
liaise with KOL, physicians, CROs, data analysts
sdafgabgfda