About the Role The Clinical Research Associate (CRA) is primarily responsible for ensuring the
rights and wellbeing of trial participants are protected and the reported trial
data are accurate, complete, and verifiable from the source documents. The CRA
is the primary contact between the Investigational Sites, Novotech, and Sponsor.
Key responsibility of a CRA is as a site relationship manager ensuring that
clinical trials are conducted in accordance with ICH GCP guidelines, local and
global regulatory requirements, and Novotech/Client SOPs. Responsibilities * CRAs primary responsibility is to build relationships with Principal Investigators, study co-ordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited, and smooth management of clinical trials. * Foster internal and external customer relationships to ensure focus on efficient, timely and productive project delivery as per study requirements and timelines. * In collaboratio...