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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:
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- 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
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