- Experience
- Any
- Salary
- —
- Openings
- 1
- Posted
- 1 hour ago
- Work mode
- In office
- Education
- Medical Doctor (MD)
- Resume
- Required to apply
Where you'll work
Job description
Role Overview
Become part of a global team of physicians dedicated to shaping the process through which new medicines are tested and reach patients. This role offers substantial influence over clinical trial design, safety protocols, and regulatory approaches rather than merely following procedural tasks.
About the Employer
The employer is a privately held, full-service Contract Research Organization (CRO) with over three decades of experience supporting clinical trials internationally. They are recognized for carefully selecting studies, delivering high-quality outcomes in a timely manner, and fostering an inclusive and collaborative medical team culture.
Key Responsibilities
- Provide medical advice to clients, project teams, trial sites, Data Safety Monitoring Boards (DSMBs), regulators, and vendors.
- Offer medical inputs on clinical development strategies, protocols, investigator brochures, clinical study reports, manuscripts, and scientific communications.
- Review clinical data to ensure patient safety and adherence to study protocols and Good Clinical Practice (GCP).
- Oversee and manage safety concerns arising from clinical sites and study teams.
- Support activities related to bidding and pharmacovigilance.
- Identify risks within clinical programs and collaborate with Clinical Operations to develop risk mitigation strategies.
- Lead or participate in advisory boards and safety monitoring boards for clinical development.
- Train and mentor clinical monitors and investigators.
- Review and approve clinical documentation for medical relevance.
Required Qualifications and Experience
- Holds a Medical Doctor (MD) degree, mandatory.
- Board certification in Gastroenterology is preferred but not compulsory.
- Clinical expertise in key therapeutic areas such as Oncology, Infectious Diseases, Gastroenterology, Hematology, or Internal Medicine is advantageous.
- Previous experience in clinical research or working within a CRO setting is strongly preferred.
- Understanding of local regulatory environments and experience interacting with health authorities is highly desirable.
- Strong skills in communication, leadership, and managing multiple stakeholders effectively.
Additional Information
This position is based in Singapore or Malaysia and requires onsite presence with a hybrid working model. Interested candidates are encouraged to apply or have confidential discussions regarding the role. The recruiting firm is a licensed entity registered under BeathChapman Pte Ltd (License no. 16S8112, Reg. No. R1110770).