WalthamFull TimeHealthcare
Remotely
pharmacovigilanceclinical trialsregulatorygood clinical practicedata interpretationtranslational strategiesclinical study design
Job Description
📋 Description
- Oversees direction, planning, and interpretation of clinical trials in oncology
- Participates in cross-functional teams to deliver data supporting strategy
- Designs development programs aligned with Product Development Plan
- Oversees study enrollment, timelines, and data safety reviews
- Mentions regulatory discussions and compliance with GCP
🎯 Requirements
- Medical Doctor (M.D.) or equivalent with relevant oncology focus
- 2+ years of clinical trial experience in pharma or academia
- Ability to run a mid-to-large clinical program with minimal supervision
- Strong cross-functional collaboration and communication skills
- Knowledge of trial methodology and regulatory requirements
- English communication skills
🎁 Benefits
- Competitive compensation with benefits
- Long-term incentive programs eligibility