To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information
Life science graduate/post-graduate, pharmacy, nursing, other healthcare related qualification. relevant experience in Pharmacovigilance including hands-on experience of drug safety, aggregate reports, signal detection/signal management preferred
Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs.
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 : Associate trainee Clinical Data Coordinator
Entry of clinical data into Clinical Data Management Systems and administration of documents to produce efficient, quality data management products that meet customer needs.
Bachelors Degree in life sciences or other related field required. Prepare and distribute status, tracking and project finance reports, and assist the project manager with budget allocation and approval of invoices.
Coordinate for lab samples collection and logistics; review of lab reports and update PI. Review & implement appropriate recruitment/referral activities for active enrollment at sites.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.