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    Medical Monitor - Singapore/Malaysia

    Ethos BeathChapman

    SingaporeInternship30 Jul 2026

    About this internship

    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