IQVIA Clinical Research Job vacancies for Life sciences Candidates
IQVIA looking to hire CRCS (Clinical Research Coordinator).
The candidate will be responsible for coordination of the study at the sites, to review adherence to Good Clinical Practice and Local Regulatory and Ethics committee requirement (EC), to review compliance with the approval protocol and study related procedures.
Qualification & Experience : Graduation / Post graduation in Life Sciences or similar discipline.
Experience : 01 to 03 years
JOB PROFILE :
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies / originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator’s Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
Location: Bangalore & Bhubaneswar. Joining: Immediate
Please share applications mentioning the preferred location at [email protected] with subject line “Application for CRCS”
