Are you looking to build a career in clinical research? This Clinical Trial Assistant (CTA) job in Bengaluru offers the perfect opportunity for candidates with 6 months to 1 year of experience to grow within a leading research environment. If you have strong organizational skills, a passion for clinical operations, and the ability to support Trial Master File (TMF) activities, this role could be your next step.
This opening is ideal for professionals aiming to work closely with Clinical Research Associates (CRAs) and Regulatory & Start-Up (RSU) teams while developing industry-relevant expertise in GCP, ICH guidelines, documentation handling, and clinical trial coordination.
Key Responsibilities
As a Clinical Trial Assistant, you will:
- Support CRAs and RSU teams in maintaining and updating the Trial Master File (TMF) and other clinical systems.
- Handle, distribute, file, and archive clinical study documents and reports following SOPs and project timelines.
- Assist in periodic review of study files for completeness and compliance.
- Support with Clinical Trial Supplies management and tracking activities.
- Track and manage Case Report Forms (CRFs), data queries, and data flow.
- Act as a central communication point for project documentation and correspondence.
- Accompany CRAs on site monitoring visits after completing required training.
Required Qualifications
- 6 months to 1 year of experience in Clinical Research / CTA roles.
- Graduate degree or equivalent education and training.
- Good working knowledge of Microsoft Word, Excel, PowerPoint.
- Strong verbal and written communication skills in English.
- Time management, organization, and multitasking abilities.
- Ability to maintain effective working relationships with cross-functional teams.
- Basic awareness of GCP, ICH guidelines, and clinical research regulations.
- Understanding of protocol requirements (training will be provided).
Benefits of This Role
- Opportunity to build a stable career in clinical operations.
- Hands-on exposure to TMF management, regulatory documentation, and clinical site coordination.
- Work with experienced CRAs and RSU professionals.
- Skill development in clinical data handling and study documentation management.
- Fast-paced learning environment for early-career researchers.
How to Apply
Eligible candidates can send their updated resume to:
📩 career@samahitha.com
