Role
This position contributes to the implementation of the global development strategy by leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds at various stages of clinical development, including clinical trial implementation and oversight of clinical development activities with the Medical Director and cross-functional teams to deliver high-quality, timely outcomes.
Responsibilities
- Lead/co-lead one or more clinical trials and oversee clinical development aspects.
- Contribute to program strategy and the clinical development plan (CDP).
- Collaborate with the Medical Director to develop clinical/regulatory documents (protocol, ICF, IB, annual safety updates, study reports, regulatory submissions).
- Support eCRFs, eCRF completion guidelines, and data management deliverables (e.g., database lock).
- Develop and execute the medical data review plan (MDRP); review and summarize efficacy/safety data.
- Provide medical input for country/site selection, feasibility, and KOL interaction.
- Prepare charters and coordinate committee meetings (Dose Escalation Committee, DMC, Steering Committee, Safety Committees).
- Develop/review study plans; liaise with project teams and CROs.
- Support publications with Scientific Communications.
- Prepare presentations for investigator meetings and training/SIVs.
- Mentor junior Clinical Research Scientists as needed.
Requirements
- PhD, PharmD, MS, or equivalent (medical/biological/pharmaceutical science or related).
- 6+ years in clinical research; 3+ years drug development experience (preferably oncology).
- Experience in project-oriented matrixed teams; strong GCP knowledge.
- Proven teamwork; can work under pressure with tight timelines.
- Strong clinical research knowledge and communication skills.
Benefits (US)
401(k) match; health/dental/vision; paid time off; 12 weeks discretionary paid parental leave; backup care and wellness support; tuition reimbursement; commuter benefits; Lifestyle Spending Account.