Offer summary
Qualifications:
MD, DO, MBBS, or equivalent medical qualifications., 5+ years of clinical experience., 5+ years in oncology clinical research., Expertise in oncology drug development lifecycle., Willingness for domestic/international travel (30% required)..
Key responsabilities:
- Ensure accuracy and integrity of trial data.
- Support business development activities and client engagement.
- Collaborate on regulatory strategies and compliance.
- Review and edit clinical trial-related documents.
- Participate in feasibility discussions and process improvements.