- 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
