Clinical Trial Manager (Cardiovascular, Renal & Metabolic Disease (CVRM)
Detalhes do emprego
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 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. 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. #J-18808-Ljbffr
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