Role : Senior Clinical Process Associate
Location : Mumbai/Bangalore
Experiences: 3- 7 Years
Key skills : Clinical Trial, CTMS, Site Selection, CTA ,Clinical Trial Associate
Senior Clinical Process Associate at IQVIA, you will play a key role in supporting clinical research operations by ensuring the accuracy, quality, and timeliness of essential clinical trial documentation and processes. This role involves collaboration with global clinical teams, coordination of study activities, and adherence to regulatory and sponsor-specific requirements.
Responsibilities:
- Manage and review essential clinical documents throughout the lifecycle of clinical trials.
- Coordinate document tracking, processing, and filing activities in compliance with ICH-GCP and SOPs.
- Support Trial Master File (TMF) management, quality control, and audit readiness.
- Communicate with internal and external stakeholders to resolve documentation issues.
- Assist in study startup, maintenance, and close-out activities.
- May mentor or support junior team members in daily activities.
- Contribute to process improvements and operational efficiency within the team.
Requirements:
- Bachelor’s degree in Life Sciences or related field (preferred).
- 3- 7 Years years of experience in clinical research or clinical document management.
- Strong understanding of clinical trial processes and regulatory documentation requirements.
- Proficient in Microsoft Office and clinical systems (e.g., eTMF, CTMS).
- Excellent organizational, communication, and teamwork skills.
Interested candidate please share your updated resume to navitha.gouli@iqvia.com