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Clinical Research Manager

2 months ago

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

Medpace is seeking a Clinical Trial Manager/Director for Clinical Trial Management specializing in Cardiovascular, Renal, and Metabolic Diseases (CVRM) to oversee global clinical research initiatives. This role is based in our Singapore office and is integral to our mission of delivering high-quality clinical services.

Key Responsibilities:
  • Oversee daily project operations, ensuring compliance with contractual obligations and adherence to ICH/GCP standards, as well as relevant regulations;
  • Act as the primary liaison for the Sponsor regarding operational project matters and study outcomes;
  • Maintain comprehensive knowledge of study protocols, therapeutic areas, and specific indications;
  • Provide cross-functional leadership to internal project teams, ensuring all necessary training is delivered;
  • Review and contribute to study protocols, data analysis plans, and final reports as needed;
  • Develop and implement operational project strategies;
  • Conduct risk assessments and manage their execution;
  • Oversee study vendors as required;
  • Ensure quality monitoring and site deliverables are met.
Qualifications:
  • Bachelor's degree or higher in a health or life sciences discipline;
  • A minimum of two years of experience in clinical trial management within the Asia Pacific region, with relevant indications being advantageous;
  • Prior experience with 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) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device sectors. Our goal is to expedite the global development of safe and effective medical therapies through a scientific and methodical approach. We utilize local regulatory and therapeutic expertise across various domains, including oncology, cardiology, metabolic diseases, endocrinology, and more. With a workforce of over 5,000 professionals across more than 40 countries, we are committed to excellence.

Why Choose Medpace?

At Medpace, we value our people, purpose, and passion. Join us in making a significant impact on the lives of patients and families affected by numerous diseases across key therapeutic areas.

Medpace Benefits:
  • Hybrid work-from-home options (depending 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 for expertise, quality, and reliability.
Next Steps:

A member of the Medpace team will review your qualifications, and if your profile aligns with our needs, you will be contacted regarding the next steps in the hiring process.

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