Director​/Snr Director, Clinical Development

We are seeking an experienced Medical Monitor/ Senior Medical Director to provide strategic and hands-on medical leadership in guiding the clinical development whilst collaborating across other divisions including Clinical Operations, Regulatory & Medical Affairs.

Some of the responsibilities include:

• Supervise clinical trials, ensuring SOPs, GCPs and following regulatory requirements.
• Serve as Medical Monitor for clinical trials, providing medical oversight and ensuring patient safety.
• CRO oversight of complex protocol procedures.
• Contribute to clinical and regulatory documents (protocols, IBs, ICFs, CSRs) and support health authority interactions.
• Collaborate cross-functionally with Clinical Operations, Regulatory Affairs, Biometrics, and Translational Medicine.
• Engage with investigators, KOLs, and study sites to ensure high-quality trial execution and scientific alignment.

Requirements:

• MD or DO (or international equivalent) with board certification or eligibility.
• 4+ years of clinical trial and medical monitoring experience in a Pharmaceutical company/CRO
• Strong understanding of Immunology drug development, safety assessment, and global regulatory requirements.
• Experience reviewing and managing SAEs, DLTs, and safety narratives.
• Excellent communication skills with the ability to engage internal teams, investigators, and regulators.
• Good communication with internal and external partners/stakeholders.

Offer:

• Competitive salary ($230-300k)
• Professional development and potential for upward career growth.