Clinical Research Associate Jobs in India

Clinical Research Associate at IQVIA Biotech partners with biotech companies to accelerate clinical development. Responsible for onsite monitoring of clinical trial sites, ensuring compliance with GCP, ICH, and sponsor protocols.

Clinical Research Associate at AstraZeneca in Bangalore, responsible for site initiation, monitoring, and closure of clinical trials. Works closely with local study teams, ensuring GCP compliance, data integrity, and timely regulatory submissions.

Clinical Research Associate II at Fortrea Development India Private Limited in Bangalore. The role monitors clinical trials, ensuring GCP compliance, data integrity, and site readiness while coordinating with sponsors and study teams.

Bristol Myers Squibb’s Clinical Research Associate team drives the integrity and compliance of global trials, ensuring patient safety and data quality. The role conducts site qualification, monitoring, and close‑out visits, manages risk‑based monitoring, and supports regulatory audits.

AstraZeneca’s Clinical Research Associate team in Bangalore drives the delivery of clinical studies, ensuring compliance with ICH-GCP and local regulations. The role monitors study sites, manages data quality, and coordinates with investigators to meet recruitment and safety milestones.

Clinical Research Associate at AstraZeneca supports oncology clinical trials in India. Responsible for site selection, qualification, training, and monitoring visits.

Clinical Research Associate on Merck's Clinical Operations team, responsible for ensuring protocol compliance and site performance across India. Manages site monitoring activities, regulatory documentation, and data quality while collaborating with investigators and cross‑functional partners.

Study Delivery team at AstraZeneca ensures clinical studies are executed efficiently and in compliance with regulations. The Clinical Research Associate manages site initiation, monitoring, and closure across Ohio and Michigan, performing both onsite and remote visits, data verification, and regulatory documentation.

Clinical Research Associate II on the PPD Development team at Thermo Fisher Scientific, driving clinical monitoring and site management for oncology and ophthalmology trials. The role conducts remote and on‑site visits, applies risk‑based monitoring, ensures protocol compliance, and collaborates with investigators to maintain audit readiness.

Clinical Research Associate I supports site management and regulatory compliance for Abbott clinical trials in India. Works with US and EMEA teams to collect, review, and upload essential regulatory documents, ensuring adherence to GCP and GDP standards.

Support site management for clinical trials in India, ensuring regulatory documents are accurate and complete per GCP/GDP. Maintain trial data systems, create binders, manage inventory, handle import/export, translate documents, and collaborate with US/EMEA teams.

Clinical Research Associate I at Abbott supports site management and regulatory compliance across clinical trials in India. Responsible for collecting and reviewing essential regulatory documents, maintaining trial information in Study Organizer, creating patient and regulatory binders, and ensuring GCP/GDP adherence.

Clinical Research Associate I supports site management and regulatory compliance for Abbott clinical trials in Gurgaon, India. Works with US and EMEA teams to collect, review, and upload essential site documents per GCP and GDP standards.

Clinical Research Associate II on the Clinical Monitoring team at Fortrea, responsible for overseeing site management and ensuring compliance with ICH GCP guidelines across clinical studies. The role conducts site monitoring visits, manages data integrity, handles regulatory documentation, and coordinates travel to study sites.

Clinical Research Associate at MSD Pharmaceuticals in Mumbai, responsible for managing site relationships and ensuring compliance with ICH-GCP and sponsor SOPs. Conducts remote and on-site monitoring, site visits, and regulatory documentation reviews to protect subject safety and data integrity.

Clinical Research team at Merck conducts ophthalmology trials across the United States. The Senior Clinical Research Associate manages site relationships, ensures protocol compliance, and leads monitoring activities both remotely and on‑site, mentoring junior CRAs.

Clinical Operations at Bristol Myers Squibb drives the execution of global clinical trials to bring innovative therapies to patients. The Senior Clinical Research Associate oversees site qualification, monitoring, and close‑out activities, ensuring compliance with protocol, ICH GCP, and regulatory standards while mentoring junior staff.

Senior Clinical Research Associate at IQVIA responsible for monitoring clinical trial sites across multiple U.S. locations. Conducts site visits, ensures compliance with GCP and ICH, manages protocol training, and oversees recruitment, enrollment, and data collection.

Initiation Clinical Research Associate I at Parexel in Bengaluru. The role drives startup, pre‑SIV and activation tasks, managing site agreements, IRB submissions, and trial master file documentation.