Clinical Research Coordinator

IQVIA Holdings Inc.

Ahmedabad, India

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.

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 Qualification: Life sciences graduate Eligibility criteria: Good verbal & written English communication skills Must speak, read & write regional language Basic knowledge of MS word & excel

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

2020-06-03 00:00:00

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