Are you passionate about clinical research and regulatory operations? IQVIA, a global leader in healthcare and life sciences solutions, is hiring Clinical Trial Assistant (CTA 2) professionals in Bangalore. This role offers a chance to support clinical teams, manage Trial Master File (TMF) documentation, and contribute to advancing innovative therapies that improve patient outcomes.

Key Responsibilities

As a Clinical Trial Assistant (CTA 2) at IQVIA, you will:

• Assist Clinical Research Associates (CRAs) and Regulatory & Start-Up (RSU) teams with TMF updates and compliance tracking.
• Manage preparation, handling, filing, and archiving of essential clinical documentation and reports.
• Support review of study files for completeness and accuracy.
• Coordinate clinical trial supplies, case report forms (CRFs), and data queries.
• Act as the central communication point for clinical team documentation and correspondence.
• Accompany CRAs on monitoring visits after required training.
• Ensure adherence to Good Clinical Practice (GCP) and ICH guidelines.

Required Qualifications

To qualify for this position, candidates should have:

• High School Diploma (or equivalent); higher qualifications in Life Sciences or Pharmacy preferred.
• 3–4 years of administrative support experience.
• At least 1 year of clinical research or related healthcare experience (preferred).
• Strong computer skills: Microsoft Word, Excel, PowerPoint.
• Good written and verbal communication in English.
• Solid organizational and time management skills.
• Knowledge of GCP, ICH, and protocol requirements (training provided).

Benefits of Working with IQVIA

• Work with one of the world’s top clinical research organizations.
• Exposure to global clinical trials and regulatory documentation systems.
• Career advancement in clinical trial management and regulatory operations.
• Collaborative work environment with leading healthcare professionals.
• Competitive salary and benefits package.

How to Apply

Application Link