Contract Type:

Permanent

Location:

Singapore, Singapore

Date Published:

30-Jul-2026

Salary:

• Join an international team of physicians shaping how new medicines reach patients
• Genuine scope to influence trial design, safety strategy and regulatory strategy, not just execute process

Our client is a privately-owned, full-service CRO with a 30-year track record supporting clinical trials across multiple continents. Known for being highly selective about the studies they take on, they've built a reputation for high-quality, timely delivery across a broad range of therapeutic areas - and a genuinely international, inclusive medical team culture. They are now looking for a Medical Monitor to join their global Medical Monitoring team, based in Singapore or Malaysia on a hybrid working arrangement. The Role You'll sit at the frontline of medical science - working across sponsors, sites, data safety monitoring boards and regulatory agencies to protect patient safety and drive high-quality clinical trial delivery. What you'll do:

• Advise clients, project teams, sites, DSMBs, regulators and vendors on medical matters
• Contribute medical input into clinical development plans, protocols, investigator brochures, CSRs, manuscripts and scientific presentations
• Review clinical data to safeguard participant safety and ensure protocol/GCP compliance
• Manage safety issues arising from sites and study teams
• Support bid defense meetings and pharmacovigilance activities
• Identify program risks and build mitigation strategies with Clinical Operations
• Chair or contribute to clinical development advisory boards and safety monitoring boards
• Train and mentor clinical monitors and investigators
• Review and sign off on clinical documents for medical relevance

What You'll Bring

• Medical Doctor degree (required)
• Board certification in Gastroenterology (preferred)
• Clinical background in a major therapeutic area - Oncology, Infectious Disease, Gastroenterology, Hematology or Internal Medicine - is a plus
• Prior clinical research / CRO experience strongly preferred
• Familiarity with local regulatory frameworks; health authority interaction experience is a strong asset
• Strong communication, leadership and stakeholder management skills

Interested candidates, or those who'd like a confidential conversation about the role, are encouraged to apply now or reach out directly. AM Reg. No. R1110770 BeathChapman Pte Ltd Licence no. 16S8112