Join a billion dollar global pharmaceutical company Be part of developing 2 portfolios - BioPharma and Oncology About Our Client A global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. Job Description Local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The SrCRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner. The SrCRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study. The Successful Applicant Bachelor degree in related discipline, preferably in life science, or equivalent qualification (.). 5+ years of relevant background in clinical research. Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP. Good knowledge of relevant local regulations. Basic understanding of the drug development process. Good understanding of Clinical Study Management including monitoring, study drug handling and data management. What's on Offer Onsite Succession planning Competitive package Contact Eds Manuel Quote job ref JN-062023-6100519 Phone number +63 02 7795 2813