Compliance jobs in Singapore

Medpace is a scientifically led organization offering full-service solutions for our clients, giving project teams the empowerment to lead and execute clinical trials.

Job type: Full-time

Singapore 138538 • Hybrid work

Job Summary: Medpace is currently looking for an experienced Clinical Trial Manager (CTM) to lead global clinical research studies. The CTM is the lead role for multiservice global/regional clinical trials, interacting with sponsors and sites and managing the timeline and project deliverables (excluding finance). This role coordinates all services contracted for the study, leading the cross-functional team through all life cycles of the project (from startup to database lock and closure). The CTM will attend bid defense meetings and support business development activities as needed. This position is fully office based in our Singapore office.

Responsibilities:

• Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all applicable laws, rules, and regulations.
• Serve as primary Sponsor contact for project-specific issues and study deliverables.
• Maintain in-depth knowledge of the protocol, therapeutic area, and indication.
• Provide cross-functional oversight of project team members and deliverables, including ensuring all necessary project-specific training is provided.
• Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report when applicable.
• Develop operational project plans.
• Manage risk assessment and mitigations.
• Manage study vendors.
• Manage site quality, including direct supervision of project Clinical Research Associates (CRAs) and monitoring deliverables.

Qualifications:

• Bachelor’s degree or higher in health/life science related field.
• At least two years of clinical trial management experience in the Asia Pacific region; indications of interest a plus.
• Prior CRO experience is preferred.
• Excellent communication skills including good verbal and written English.
• Flexible, accountable, and comfortable working in a global environment.

Medpace Overview: Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Medpace Perks:

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards:

• Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next: A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.