IQVIA, a global leader in clinical research and healthcare intelligence, is hiring a Clinical Process Associate in Bengaluru, Karnataka. This role is critical in supporting clinical operations by ensuring high-quality deliverables, compliance with SOPs, and adherence to regulatory requirements.
Key Responsibilities:
- Provide project-related assistance for assigned clinical studies, sites, and project teams.
- Ensure all tasks comply with SOPs, GCP (Good Clinical Practice), and regulatory guidelines.
- Perform processes related to Start-Up or Maintenance studies, maintaining timelines and SLAs.
- Manage document creation, review, and maintenance, including tracking tools and databases.
- Participate in study team meetings and implement action items.
- Assist in visit tracking (CTMS), investigator payments, vendor setup QC, PV batch review, and invoice processing.
- Handle access provisioning, ATP (Authorization to Proceed) training reviews, and coordination with translation vendors.
- Support contract understanding and quality control for processing teams.
- Provide administrative support, indexing, and ad-hoc data requests.
- Mentor new hires (buddy system) and act as an SME (Subject Matter Expert) for the team.
Qualifications & Experience:
- Bachelor’s Degree (Life Sciences preferred).
- Minimum 2 years of relevant experience in clinical operations or related fields.
- Strong understanding of clinical trial processes, regulatory compliance, and document management.
- Ability to work in a fast-paced, deadline-driven environment.
- Excellent communication, organizational, and problem-solving skills.
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences industry. With a focus on accelerating drug development and improving patient outcomes, IQVIA delivers intelligent insights that drive healthcare innovation.
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