The Clin Process Associate position at IQVIA in Bengaluru, Karnataka, India is a full-time role focused on providing support for clinical projects and ensuring quality and compliance with applicable standards. The associate will assist with various tasks within the clinical operations team, contributing to both start-up and maintenance phases of studies.
Key Job Responsibilities:
- Perform tasks that lead to high-quality project deliverables, adhering to SLAs and project timelines.
- Manage documentation and maintain effective project/site communications.
- Update and monitor internal systems, databases, and project tools.
- Participate in document creation, review, and management.
- Attend study team meetings and implement related action items.
- Collaborate on the creation/review of study documents and set quality standards.
- Handle tasks related to CTMS tracking for Investigator payments, vendor setup quality checks, and invoice reviews.
- Coordinate access management and review training authorizations.
- Communicate with translation vendors and manage contract-related processes.
- Provide administrative support and help in activity tracking.
- May serve as a mentor to new hires and act as an SME for the team.
Qualifications:
- Bachelor’s Degree (preferred)
- Life Sciences graduates with a minimum of 2 years of relevant experience (preferred)
IQVIA is a global leader in clinical research services and healthcare intelligence, supporting the life sciences industry in developing innovative treatments and improving healthcare outcomes. More information about the company and career opportunities can be found at IQVIA’s career site.