Clinical Trial Manager (Cardiovascular, Renal & Metabolic Disease (CVRM)

Medpace; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a dedicated Clinical Trial Manager to spearhead global clinical research studies in Singapore. This pivotal role involves leading cross-functional teams, managing timelines, and ensuring project deliverables are met. Ideal candidates will have a strong background in clinical trial management, particularly within the Asia Pacific region, and experience in Cardiovascular, Renal & Metabolic Disease studies. Join a scientifically driven organization that empowers its project teams to excel in clinical trials, offering a dynamic environment where your contributions will make a significant impact on global health research.

Qualifications

• 2+ years of clinical trial management experience, ideally in a CRO environment.
• Experience in Cardiovascular, Renal & Metabolic Disease studies required.

Responsibilities

• Lead global clinical trials and manage project timelines and deliverables.
• Coordinate services contracted for the study and lead cross-functional teams.

Skills

Clinical Trial Management

Communication Skills

Project Management

Regulatory Knowledge

Education

Bachelor’s degree in a health-related field

Master’s degree or PhD

Job description

Job Summary

Medpace is currently looking for full-time Clinical Trial Manager (CTM) in Singapore to lead global clinical research studies. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials.

Responsibilities

The Clinical Trial Manager position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates for all services contracted for the study. CTMs are also responsible for leading cross-functional teams of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring, etc. CTMs may need to attend bid defense meetings and support the business development team in winning new business.

Qualifications

• Bachelor’s degree in a health-related field (Master’s degree or PhD is preferred);
• At least two years of clinical trial management experience in the Asia Pacific region, ideally in a CRO environment;
• Experience in Cardiovascular, Renal & Metabolic Disease (CVRM) studies required;
• Excellent communication skills including good written and spoken English; and
• Flexible, accountable, and comfortable in working in a global environment.

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for the next steps.

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