Clinical Trial Manager (Oncology/Cardiovascular)
Overview:
A leading CRO has partnered with Apsida Life Sciences, providing 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 a 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, employing more than 5,000 people across 40+ countries.
Job Title: Clinical Trial Manager (Cardiovascular, Oncology, Renal & Metabolic Disease (CVRM))
Responsibilities:
The Clinical Trial Manager position performs a project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates all services contracted for the study. CTMs are also responsible for leading a cross-functional team of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring, etc. The CTM 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;
- Flexible, accountable, and comfortable working in a global environment.
Seniority level
Mid-Senior level
Employment type
Full time
Job function
Health Care Provider, Research, and Science
Industries
Research Services and Biotechnology Research
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