Clinical Trial Assistant (CTA) – Clinical Research Operations
Location: Delhi, India (Office-Based)
Company: Insignia Clinical Services Pvt. Ltd.
Open Positions: 04
Employment Type: Full-Time
Experience Required: Minimum 1 Year
Application Email: careers@insigniacs.com
About the Company
Insignia Clinical Services Pvt. Ltd. is a clinical research organization committed to delivering high-quality clinical trial management services. With a strong focus on regulatory compliance, operational excellence, and ethical research conduct, the organization supports sponsors and investigative sites across therapeutic areas.
Role Overview
The Clinical Trial Assistant (CTA) will support clinical trial operations by ensuring accurate documentation, regulatory compliance, and effective site coordination. This position is ideal for early-career clinical research professionals seeking hands-on exposure to study management, Trial Master File (TMF) maintenance, and GCP-compliant trial execution.
Key Responsibilities
Support day-to-day clinical trial operations and study documentation management.
Maintain and update Trial Master File (TMF) and essential study documents in compliance with ICH-GCP guidelines.
Assist with investigator site coordination and communication.
Track study milestones, regulatory submissions, and document version control.
Support internal teams in ensuring inspection readiness and audit compliance.
Coordinate communication between sponsors, CRO teams, and investigative sites.
Required Experience
Minimum 1 year of relevant experience in:
Clinical Trials
Clinical Trial Assistant (CTA) role
Clinical Research Coordinator (CRC) role
Strong understanding of ICH-GCP guidelines and clinical research processes.
Familiarity with TMF management and essential documentation standards.
Educational Qualifications
Master’s Degree in Life Sciences or related field
OR
Bachelor of Pharmacy (B. Pharma)
Core Competencies
Strong organizational and documentation skills
Good understanding of regulatory and ethical requirements in clinical research
Effective written and verbal communication
Ability to manage multiple tasks and meet study timelines
High attention to detail and compliance orientation
Why Apply
This opportunity offers structured exposure to clinical operations, regulatory documentation, and site coordination within a professional clinical research environment. Candidates looking to build long-term careers in Clinical Operations, Clinical Project Management, or Regulatory Affairs will benefit from this role.
How to Apply
Interested candidates can share their updated CV at:
careers@insigniacs.com
Company Website: www.insigniacs.com
SEO Keywords:
Clinical Trial Assistant Jobs Delhi, CTA Jobs India, Clinical Research Coordinator Careers, TMF Management Jobs, GCP Clinical Research Roles, Entry Level Clinical Operations Jobs, CRO Jobs Delhi, Insignia Clinical Services Careers.
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