BioTalent are delighted to partner with an exciting European biotech client looking to hire a clinical scientist to join their small, growing U.S team.
Reporting to the Vice President, Clinical Development and supporting the global medical director, your responsibilities will include:
Writing clinical protocol related documents (including amendments, informed consents)
Working closely with the clinical operations team to support global study start up activities, including site activation, subject enrollment and monitoring
Reviewing and interpreting clinical data
Identifying and mitigating any risks to clinical study execution
Active participation in investigator meetings and engagement
Training site staff and internal colleagues on the study protocol
Ideally, you will have:
An advanced degree (PharmD, PhD, MD) or otherwise BS, BSN as a minimum
Over 3 years dedicated clinical development experience in a pharma or biotech environment
Strong working knowledge of oncology
Expertise in clinical evaluation projects, including development of protocols and case report forms
Excellent written and communication skills
Get in touch with Ella Jobson for a confidential discussion on +1 424 2773748 / ella.jobson@biotalent.com or click apply