Clinical Trial Manager
CN-Beijing
International Careers
Req #: 11231
Type: Full-Time
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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. 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. Our full-service approach is led by medical, regulatory and operational experts with deep therapeutic experience. The disciplined processes, site relationships, and technologies enable CTMs to execute even the most complex global studies. Therapeutic focus areas including oncology, cardiovascular, endocrine/metabolic, infectious disease, CNS. Trials include those in rare disease and Advanced Therapies. 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; * Excellent planning, organisation, prioritisation skills; and * Flexible, accountable and comfortable in working in a global environment.
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