IQVIA looking for Clinical Research Coordinator

IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

Post : Clinical Research Coordinator

Job Description
• Conduct site/trial feasibility to identify & select the right site and investigator for the study
• Ensure timely compilation of all essential documents & assist in regulatory package preparation, timely submission, follow up with site EC to resolve any queries, and obtain approvals
• Ensuring site setup according to protocol, review patient data base & pre-screening, identify physician network
• Coordinate for Clinical Trial Supplies receipt, accountability & storage
• Prepare site team for study initiation visit and coordinate with monitor for the visit
• Assist in the process of administering the informed consent to the potential objects and discussing in detail the patient information sheet
• Ensure that site documentation remains current, accurate and complete
• Coordinate for lab samples collection and logistics; review of lab reports and update PI
• Review & implement appropriate recruitment/referral activities for active enrolment at sites
• Ensure CRF Completion and query resolution on specified timelines
• Coordinate in conduct of monitoring visits and audits (Internal or External)
• Ensure that monitoring/audit related findings are resolved within the timelines
• Ensure patient follow up visit and visit compliance; manage patient related reimbursement; site related payment
• Drug receipt, accountability, storage, dispensing and related documentation
• Ensure adherence to protocol guideline, regulations, ethical guidelines
• Coordinate and ensure timely reporting to all stakeholders
• Maintain study log(s) & study manuals
• Assist monitor with the site closeout activities
• Manage final reconciliation of Clinical Trial Supplies and archival of study documents at sites

Candidate Profile
• Bachelor's Degree Bachelor's Degree in life sciences or other related field required Req
• Typically requires 2-3 or more years of experience.
• Requires good knowledge within a specific discipline typically gained through extensive work experience and/or education.
• 4 – 5 years’ experience or equivalent comination of education, training, and experience.
• Knowledge of clinical trials - basic knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;
• Communication - strong written and verbal communication skills including good command of English language. Good communication and interpersonal skills.
• Problem solving - good problem solving skills.
• Quality - results and detail-oriented approach to work delivery and output. Good planning, time management, and prioritization skills. Attention to detail and accuracy in work.
• IT skills - good software and computer skills, including MS Office applications.
• Collaboration - ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Cross-collaboration - ability to work across geographies displaying high awareness and understanding of cultural differences.

Additional Information
Location : Mumbai
Industry Type : Pharma/ Healthcare/ Clinical research
Job ID : R1503449
End Date : 30th December 2025