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Lead Physician for Clinical Trials in Oncology
2 months ago
As a Lead Physician for Clinical Trials in Oncology, you will play a pivotal role in overseeing multiple clinical studies, ensuring the highest standards of medical accountability and oversight.
Key Responsibilities:
1. **Medical Oversight:**
- Act as the primary medical authority for various clinical trials.
- Collaborate with cross-functional teams to ensure compliance and adherence to safety protocols.
2. **Clinical Development Expertise:**
- Design and implement clinical plans and protocols, focusing on strategic objectives.
- Analyze benefit/risk assessments in collaboration with Clinical Scientists.
3. **Data Review and Monitoring:**
- Lead the review of clinical trial data, ensuring eligibility and safety management.
- Interact with clinical sites to address medical inquiries and provide necessary education.
4. **Health Authority Interactions:**
- Serve as a medical expert during key interactions with health authorities and advisory boards.
- Contribute to the drafting of clinical study reports and regulatory submissions.
Qualifications:
- MD required (or equivalent).
- Minimum of 5 years of experience in the pharmaceutical industry or clinical trials.
- Strong communication skills and ability to lead presentations in scientific settings.
Work Environment:
Bristol Myers Squibb values a balanced and flexible work environment, offering competitive benefits and resources to support both professional and personal goals. We are committed to fostering an inclusive culture that promotes diversity in clinical trials and empowers employees to reach their full potential.
