Clinical Trial Manager

3 days ago

Singapur, Singapore Medpace Full time
Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (CVRM))

Join to apply for the Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (CVRM)) role at Medpace

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

Join to apply for the Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (CVRM)) role at Medpace

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 team of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring etc. CTM may need to attend bid defense meetings and support 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 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.
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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
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. Seniority level
  • Seniority level Not Applicable
Employment type
  • Employment type Full-time
Job function
  • Job function Research, Analyst, and Information Technology
  • Industries Pharmaceutical Manufacturing

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