Premier Research is hiring Clinical Trial Associate I and Clinical Trial Associate II professionals to join its Global Clinical Monitoring and Site Management team in Bangalore, India. This is an excellent opportunity for life sciences graduates and early-career clinical research professionals seeking growth in clinical operations, TMF/eTMF management, and site management within a globally recognized CRO environment.
If you are aiming to build a long-term career in clinical trials, regulatory-compliant documentation, and clinical systems (CTMS, EDC, IWRS), these roles provide strong exposure, structured training, and career progression.
๐ Job Overview
- Company: Premier Research
- Job Titles: Clinical Trial Associate I / Clinical Trial Associate II
- Location: Bangalore, India (Hybrid)
- Employment Type: Full-time
- Application Deadline: February 7, 2026
๐ Key Responsibilities
Document Management
- Maintain TMF/eTMF according to sponsor SOPs and regulatory requirements
- Create and manage TMF placeholders based on filing plans and milestones
- Review site documents for ALCOA+ and GCP compliance
- Perform completeness and quality checks across study lifecycle
- Run and distribute eTMF reports for quality oversight
- Support essential document collection during startup, maintenance, and closeout
Data Entry, Tracking & System Support
- Support CTMS setup and data entry
- Track Investigatorโs Brochure and safety report distribution
- Manage system access for CTMS, EDC, IWRS, and vendors
- Review training matrices and ensure compliance
- Assist with CRA workflows and site follow-up items
Additional Responsibilities
- Attend clinical team meetings and prepare follow-up documentation
- Liaise with vendors for translations and study equipment
- Support creation of Investigator Site Files (ISF)
- Coordinate logistics and administrative tasks
- (For CTA II) Mentor junior CTAs and support departmental initiatives
๐ Qualifications
Clinical Trial Associate I
- Bachelorโs degree in Life Sciences, Nursing, or Medical Documentation
- Fluent English communication
- Knowledge of ICH-GCP preferred
- Strong MS Office skills
Clinical Trial Associate II
- Bachelorโs degree in Life Sciences/Nursing/Medical Documentation
- Minimum 1 year experience as CTA or similar role
- Working knowledge of ICH-GCP, essential documents, ALCOA+
- Experience with CTMS and eTMF systems
๐ผ Skills Required
- TMF/eTMF management
- Clinical documentation review
- Regulatory compliance
- Strong organization & time management
- Attention to detail
- Team collaboration
๐ฐ Expected Salary (India)
- CTA I: โน4,00,000 โ โน6,00,000 per annum
- CTA II: โน6,00,000 โ โน9,00,000 per annum
(Actual salary may vary based on experience and interview performance.)
๐ Why Join Premier Research?
- Hybrid working model
- Career growth in global clinical research
- Exposure to biotech, medtech, and pharma studies
- Structured training and development
- Work-life balance culture
๐ How to Apply
Application Link For Clinical Trial Associate I
Application Link For Clinical Trial Associate II
