Offer summary
Qualifications:
MD, DO, MBBS or equivalent medical qualifications, 5+ years of clinical experience, 5+ years in oncology clinical research, Drug development experience is preferred, Board Certification in Oncology/Hematology is preferred.
Key responsabilities:
- Ensure data accuracy and patient safety
- Support Business Development and participate in RFP process
- Write and edit scientific content within budget
- Review protocols and clinical trial reports
- Collaborate for strategic drug development solutions