Senior Medical Monitor Manager

This is a fully remote position, open to applicants in Singapore.

📋 Description

• Oversee and provide medical support for clinical trials, ensuring compliance with GCP and study protocols.

• Serve as the primary medical contact for clinical development, including input on protocols, medical reviews, safety assessments, and interactions with clients and regulatory bodies.

• Evaluate and offer medical insights on protocols, informed consent documents, Investigator’s Brochures, statistical analysis plans, and various study documents.

• Engage in study start-up, monitoring, and closeout processes as required.

• Deliver medical training and support to monitors and project teams, including during investigator meetings and safety/data monitoring committees.

• Perform medical reviews of clinical data to detect any quality or safety concerns.

• Evaluate and manage adverse events and serious adverse events, which includes medical adjudication, causality assessments, and follow-up recommendations.

• Draft and review medical reports.

• Coordinate communication with investigators, sponsors, safety monitoring committees, pharmacovigilance teams, and regulatory authorities.

• Represent the company in client meetings, RFPs, and communications with ethics committees and regulators.

• Conduct product safety monitoring and prepare or review safety reports, Risk Management Plans, DSURs, and PSURs.

• Collaborate with Medical Directors/Managers and drug safety teams to address and resolve safety issues.

• Perform additional tasks as assigned by the Medical Director.

⛳️ Requirements

• Master’s degree in Medicine.

• At least 2 years of direct medical practice experience, not including postgraduate study experience.

• 7–10 years or more of professional experience.

• Over 5 years of experience in medical monitoring or as a medical manager.

• Experience with CROs or sponsors is preferred.

• Proficient in verbal and written English.

• Capable of working independently and managing multiple tasks under pressure.

• Strong communication, cross-functional coordination, and problem-solving abilities.

• Possess a global, cross-cultural perspective and a customer-focused approach.

• Familiarity with GCP and clinical trial processes.

• Able to communicate effectively with international clients and regulatory bodies.

🏝️ Benefits

• Competitive salary and benefits package tailored to skills and experience.

• Hybrid or remote working options, based on location and role.

• Opportunities for learning and access to a global network of scientific leaders.

• Employee wellbeing programs and initiatives that promote work-life balance, health, and team engagement.

• Global engagement surveys.

• Recognition programs.

• Team-building events.

• Exposure to a variety of international projects and clients.