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 / or click apply