Clinical Research Associates (CRAs) coordinate and monitor clinical trials to ensure compliance with regulatory requirements and study protocols. They play a key role in collecting data, ensuring patient safety, and maintaining the integrity of research studies in the pharmaceutical, biotechnology, and medical device industries.
₹3,00,000 - ₹10,00,000 per annum (depending on experience, expertise, and organization)
Clinical Research Associates are in demand in pharmaceutical companies, contract research organizations (CROs), hospitals, and academic research centers. Their expertise is vital for the development of new drugs, therapies, and medical devices, ensuring safety and efficacy through rigorous clinical trials.
CRAs work both in office settings and on-site at clinical trial locations. The role involves travel, collaboration with investigators and site staff, and adherence to strict regulatory standards. Attention to detail and strong organizational skills are essential.