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Lead Clinical Trial Coordinator

2 months ago

Bristol, Maine, United States Medpace Full time
Position Overview:

Medpace is seeking a Clinical Trial Manager/Director for Clinical Trial Management in Cardiovascular, Renal & Metabolic Disease (CVRM) to oversee global clinical research initiatives. This role is integral to our Singapore operations, where we empower our project teams to lead and execute clinical trials effectively.

Key Responsibilities:
  • Oversee daily project operations in accordance with contractual obligations and compliance with ICH/GCP and relevant regulations;
  • Act as the primary contact for the Sponsor regarding operational project-specific matters and deliverables;
  • Maintain comprehensive knowledge of the study protocol, therapeutic areas, and specific indications;
  • Provide cross-functional oversight to internal project team members, ensuring all necessary training is delivered;
  • Review and contribute to study protocols, edit check specifications, data analysis plans, and final study reports as needed;
  • Develop and implement operational project plans;
  • Conduct risk assessments and manage execution strategies;
  • Oversee study vendors as required;
  • Ensure quality and monitoring deliverables at study sites.
Qualifications:
  • A Bachelor's degree or higher in a health or life sciences field;
  • A minimum of two years of experience in clinical trial management within the Asia Pacific region, with relevant indications being advantageous;
  • Previous experience in a Contract Research Organization (CRO) is preferred;
  • Strong communication skills, both verbal and written in English;
  • Adaptable, responsible, and comfortable in a global work environment.
About Medpace:

Medpace is a comprehensive clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device sectors. Our mission is to expedite the global development of safe and effective medical therapies through a scientific and disciplined approach. We utilize local regulatory and therapeutic expertise across major areas, including oncology, cardiology, metabolic diseases, endocrinology, central nervous system disorders, and infectious diseases.

Why Choose Medpace?

Our commitment to People, Purpose, and Passion drives us to make a difference in the lives of patients and families facing various diseases. The work we do today will have a lasting impact on the future of healthcare.

Medpace Benefits:
  • Hybrid work-from-home options (dependent on position and level);
  • Competitive paid time off (PTO) packages;
  • Company-sponsored employee appreciation events;
  • Health and wellness initiatives for employees;
  • Flexible work schedules;
  • Attractive compensation and benefits packages;
  • Structured career paths with opportunities for professional development.
Awards and Recognition:
  • Featured by Forbes as one of America's Most Successful Midsize Companies in recent years;
  • Consistently recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
Next Steps:

A member of the Medpace team will review your qualifications and reach out with further details if your profile aligns with our needs.

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