What are the responsibilities and job description for the Clinical Trial Manager (Nephrology/Cardiovascular/Renal/GI) position at Apsida Life Science?
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 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. Employing more than 5,000 people across 40 countries.
Job Title: Clinical Trial Manager (Cardiovascular,Oncology, Renal & Metabolic Disease (CVRM))
Location: Singapore-Singapore
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
