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 ####### / ...@biotalent.com or click apply