Senior Clinical Scientist - Contractor

We are currently working with an oncology biotech who is seeking a Senior Clinical Scientist Contractor 40 hours per week.
Looking for a team-oriented individual with a successful track record within the industry. Ideal candidate will collaborate with cross functional teams such as Pharmacovigilance, Translational Medicine, Project Management, Clinical Operations, and Biostatistics.
Responsibilities
Responsible for design and development of clinical development plans.
Draft clinical protocol within IB, DSUR, INDs, and CSRs.
Oversee review of clinical study entries.
Collaborate with vendors and Investigators on specific projects.
Clinical Data review.
Deviation Review.
Experience Required
PhD, PharmD, RN, MS, BS or equivalent/advanced degree required.
Strong understanding of the drug development process from IND/CTA through BLA/NDA submission.
Veeva experience preferred and aggregate data review.
Oncology experience required.
Late-stage program experience preferred.
5 plus years of clinical research/drug development experience in pharma/biotech.

Work arrangement
Yes