Senior Initiation Clinical Research Associate
BengaluruFull-timeMid levelPosted over a month ago
Mid-level pharma role at Parexel International India safety services in Bengaluru.
About the role
When our values align, there's no limit to what we can achieve. Act as Parexel's direct point of contact with assigned sites, accountable for quality and delivery during the startup phase Support country-specific feasibility and site qualification activities, including preparation, negotiation
What you'll do
- Manage country and site-level Trial Master File (TMF) issues, ensuring First Time Quality (FTQ) documentation and providing direct resolution to reported site problems
- Develop and execute strategy for configuring, distributing, collecting, and reviewing high-quality country-specific and site-specific regulatory documents
What you need
- Clinical research
- Documentation