POSITION OVERVIEW

Mcure Biosciences Inc. is a biotechnology startup based in the San Francisco Bay Area. We are advancing novel antibody therapeutics and preparing for human clinical trials. Our mission is to bring transformative therapies to patients with high unmet medical needs worldwide.
We are seeking a highly accomplished Chief Medical Officer (CMO) to join our executive team. The CMO will be responsible for providing strategic and operational leadership for our global clinical development programs, with a focus on infectious disease and critical care indications. This individual will play a key role in shaping clinical strategy, overseeing trial execution, and engaging with key stakeholders, regulators, and investigators worldwide.

QUALIFICATIONS

• MD degree required.
• 15–20 years of hands-on clinical trial experience, including protocol design and execution.
• Proven experience in infectious diseases and/or ICU clinical trials.
• Track record of international clinical development and regulatory interactions (US, EU, Asia) preferred.
• Strong network of KOLs and CRO partners in infectious disease/critical care.
• Demonstrated ability to thrive in a startup or entrepreneurial environment.
• Excellent communication, leadership, and problem-solving skills.
• Enthusiastic, collaborative, and adaptable team player.
  Job Types: Full-time, Part-time
  Expected hours: 10 – 40 per week

Benefits:

• Flexible schedule
• Paid time off

Work Location: Hybrid remote in Sunnyvale, CA 9408

• Lead the design, implementation, and oversight of global clinical development strategies.
• Develop and review clinical trial protocols, investigator brochures, INDs/CTAs, and related documents.
• Provide medical leadership to cross-functional teams, including regulatory, clinical operations, and R&D.
• Build and manage strong relationships with CROs, investigators, and regulatory agencies in the US, EU, and Asia.
• Engage and collaborate with key opinion leaders (KOLs) in infectious disease and intensive care medicine.
• Advise the executive team and Board of Directors on clinical development strategy and progress.
• Ensure compliance with global regulatory requirements, ethical standards, and GCP guidelines.
• Represent the company in external communications, including scientific meetings and conferences.