Work as Clinical Research Coordinator at IQVIA

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 : Clin Research Coord

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
• Life sciences graduate
• Good verbal & written English communication skills
• Must speak, read & write regional language
• Basic knowledge of MS word & excel

Additional Information
Qualification : Life Sciences graduate
Location : Noida, India
Industry Type : Pharma / Healthcare / Clinical research
Req Id : R1126154
End Date : 25th May, 2020