Premier Research has announced a new Clinical Trial Associate II job in Bangalore for candidates with experience in clinical research, Trial Master File (TMF), eTMF, CTMS, and clinical trial documentation. The position is part of the Clinical Monitoring, Site Management and Study Start-Up team.
This Premier Research Clinical Trial Associate II hiring 2026 opportunity is particularly relevant for nursing, life sciences, and medical documentation graduates with 1–2 years of Clinical Trial Associate or similar experience. Premier Research is looking for candidates who can join immediately or at the earliest.
About Premier Research
Premier Research supports biotech, medtech, and specialty pharmaceutical companies in the development of medicines, medical devices, and diagnostics. The organization works across clinical development and provides opportunities for professionals to contribute to studies that support medical innovation.
Job Overview
| Particulars | Details |
|---|---|
| Company | Premier Research |
| Position | Clinical Trial Associate II |
| Location | Bangalore, India |
| Work Mode | Hybrid |
| Office Requirement | 2 days per week |
| Job Type | Full-Time |
| Experience | Minimum 1–2 years |
| Requisition ID | R5940 |
| Joining Preference | Immediate joiners |
| Estimated Salary | ₹4.5–7.5 LPA |
Salary is an editorial estimate based on comparable clinical research roles in India and is not an employer-disclosed salary.
Key Responsibilities
As a Clinical Trial Associate II at Premier Research, selected candidates will support clinical trial documentation, TMF/eTMF quality, study teams, and essential document management.
Key responsibilities include:
- Maintain the Trial Master File (TMF) and electronic Trial Master File (eTMF) according to organizational or sponsor SOPs and applicable regulatory requirements.
- Create and maintain TMF placeholders based on filing plans, study milestones, expired documents, site staff changes, and other study events.
- Review site documents to ensure compliance with company, sponsor, regulatory, and ALCOA+ requirements.
- Perform quality reviews and completeness checks of relevant eTMF sections.
- Support TMF activities throughout study start-up, maintenance, and close-out.
- Follow up with clinical teams to resolve TMF queries and identified documentation issues.
- Generate and distribute eTMF reports to clinical teams to support quality and compliance.
- Assist Study Start-Up Associates and CRAs with essential document collection and review when required.
- Support or review translations of site documents when applicable.
Qualifications
Candidates interested in the Premier Research Clinical Trial Associate II job should meet the following requirements:
- Undergraduate degree or international equivalent in Nursing, Life Sciences, or Medical Documentation from an accredited institution.
- Minimum 1–2 years of prior experience as a Clinical Trial Associate or in a similar clinical research role.
- An equivalent combination of education and relevant experience may also be considered.
- Fluent written and verbal English.
- Working knowledge of ICH-GCP, essential clinical trial documents, and ALCOA+ principles.
- Experience working with clinical research systems such as CTMS and eTMF.
- Good working knowledge of MS Word, Excel, PowerPoint, and Outlook.
- Strong organizational and time-management skills.
- Ability to meet study and documentation deadlines.
- Good interpersonal and listening skills.
- Ability to work independently and collaboratively within clinical study teams.
Key Skills
Candidates with the following skills may be particularly relevant for this Clinical Trial Associate vacancy:
Clinical Research | TMF | eTMF | CTMS | ICH-GCP | ALCOA+ | Essential Documents | Clinical Trial Documentation | TMF Quality Review | Study Start-Up | Site Management | Document QC | MS Excel
Who Can Apply?
This opportunity is suitable for candidates with an undergraduate degree in Life Sciences, Nursing, or Medical Documentation who have approximately 1–2 years of relevant Clinical Trial Associate or similar experience.
Candidates from relevant life sciences educational backgrounds may be considered where their education and professional experience collectively meet Premier Research’s requirements.
Because the employer specifically requires prior CTA or similar experience, this vacancy should not be presented as a pure fresher opening.
Why Consider This Role?
The Clinical Trial Associate II position provides exposure to important clinical operations activities, particularly TMF/eTMF management, essential document review, study start-up, maintenance, close-out, CTMS, and clinical trial compliance.
Premier Research also highlights professional development, opportunities to build new skills, employee input in how teams work, and flexibility to maintain work-life balance.
How to Apply
