Research Consultant in Clinical Research

Roles & Responsibilities
• Gain familiarity with Advarra’s Clinical Trial Management Software (CTMS), Institutional Review Board (IRB) systems, and CIRBI platform
• Support Client Services teams in translation management, safety reporting, and ongoing reviews (site termination & IRB submissions)
• Document issues, manage customer communications, and ensure smooth study start-up processes
• Monitor and resolve customer escalations in a timely manner
• Track and complete assigned tasks using internal case management software
• Meet daily/weekly productivity and quality metrics in coordination with reporting manager
• Participate in team meetings and provide insights on customer cases and study protocols
• Maintain accurate documentation aligned with GCP and regulatory standards

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

Experience
• 0–1 year of internship or relevant experience in:
– Clinical trial coordination
– Study Start-Up / Regulatory Affairs
– IRB submissions
– Clinical data management
– Records management

Skills
• Knowledge of clinical research methodology and GCP guidelines
• Understanding of study start-up and regulatory processes
• Proficiency in MS Office and business software tools
• Strong organizational and administrative skills
• Excellent written and verbal communication skills
• Strong problem-solving abilities and customer service orientation
• Ability to work independently and collaboratively in a team environment
• High attention to detail and strong time management skills

About the Company
Advarra is a global leader in clinical research solutions, providing ethical review services, regulatory expertise, and innovative technology platforms that connect patients, sponsors, CROs, and research sites to accelerate high-quality clinical trials worldwide.