Consultant - Clinical Development

Role Overview:

As a Consultant, you will serve as a clinical and scientific subject matter expert, providing hands‑on medical oversight and strategic leadership across oncology development programs. You will play a critical role in ensuring patient safety, data integrity, and scientifically sound decision‑making throughout the clinical trial lifecycle.

Key Responsibilities:

• Act as the Oncology SME for early and late‑phase oncology clinical trials, supporting patient safety oversight.
• Provide expert input into oncology trial design, protocol development, eligibility criteria, endpoints, and dose‑modification guidelines.
• In Oncology trials, review and assess serious adverse events (SAEs), adverse events of special interest, and safety signals, providing timely medical guidance.
• Partner closely with Clinical Operations, Regulatory Affairs, Medical Affairs, Pharmacovigilance, and Biostatistics to support study execution and regulatory readiness.
• Interpret emerging efficacy and safety data, literature, and competitor insights to inform development strategy and risk‑benefit assessments.
• Contribute to Data Monitoring Committees (DMCs), safety review meetings, investigator interactions, and regulatory responses.
• Drive a patient‑centric, evidence‑based approach, ensuring oncology best practices are embedded across all development programs.

Qualification:

MD (Oncology)

Experience:

2 + years of prior experience in managing oncology trials

Location:

Remote/Hybrid