Senior Manager, Clinical Research Site Monitoring (Oncology)
Sponsor Side
Hybrid - 3 Days onsite
SciPro is partnered with one of the fastest growing, Clinical Stage Biotechnology companies on the West Coast right now in the Oncology space. They are experiencing growth as a result of positive Clinical results and is actively searching for a talented individual to join the team on a permanent basis as a Senior Manager for Clinical Monitoring.
Responsibilities
- CRO Oversight of both domestic and global Clinical Trials - Specifically focused in Oncology
- Identifying and establishing relationships with new external stakeholders, such as CRO and other Clinical Sites.
- Provide oversight of qualification of new sites and maintain and improve site relationships to maximize patient and site experience
- Align company goals with new stakeholders, provide insight in to pipeline progress and ensure compliance to eQMS standards and domestic and global Regulatory guidelines
- Have non-disciplinary responsibilities over CRAs and take part in onboarding new CRAs
Requirements
- Extensive experience in qualification and management of external stakeholders, extensive CRO oversight experience
- Strong experience in CRA / CTM function within Oncology based biotech or CRO
- Minimum Bachelor’s in Scientific and/or Clinical field
- Ability to effectively utilize the CTMS and Trial Master File (TMF) to ensure SEME documents are promptly filed and site data is accurate.
- Ability to travel domestically & internationally
If this is a role that interests you then please click respond through the LinkedIn apply function or send your resume over to J.Greavesjohnson@sciproglobal.com.
