Research Associate

Roles & Responsibilities
• Interpret clinical trial protocols and design study calendars
• Develop and manage site budgets aligned with CTAs and sponsor requirements
• Ensure protocol, budget, and documentation accuracy and compliance
• Collaborate with cross-functional clinical operations teams
• Maintain study documentation and support operational readiness
• Support clinical trial execution activities across study lifecycle

Qualification
• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related field

Experience
• 1–5 years of experience in one or more of the following:
– Clinical Research Coordinator (CRC)
– Clinical Research Associate (Site level)
– Clinical Data Management
– Pharmacovigilance
– Records Management

Skills
• Good understanding of clinical trial processes
• Strong analytical and problem-solving skills
• Effective written and verbal communication
• Attention to detail and documentation accuracy
• Ability to work collaboratively in cross-functional teams

About the Organization
Advarra is a global leader in clinical research technology and services, supporting safer, smarter, and more efficient clinical trials to improve patient outcomes worldwide.