Clinical Trial Associate I Job at Premier Researchin Bengaluru with hybrid work for life sciences graduates seeking entry-level clinical research roles.
Introduction
A promising opportunity is now open for aspiring clinical research professionals who want to build a long-term career in global clinical operations. This Clinical Trial Associate I role is ideal for candidates seeking hands-on exposure to clinical trial documentation, site management, and regulatory compliance while working in a collaborative and growth-oriented environment. The position offers a balanced hybrid work model along with structured learning and career development. Clinical Trial Associate I Job
Company Overview
Premier Research is a global clinical research organization supporting biotech, medical device, and specialty pharmaceutical companies. The organization partners with innovators to bring new medicines, devices, and diagnostics to patients worldwide. With a strong focus on quality, people development, and flexibility, Premier Research provides an environment where clinical professionals can grow while contributing to meaningful healthcare advancements. Clinical Trial Associate I Job
Job Location & Employment Type
- Job Location: Bengaluru, India
- Work Scope: India
- Employment Type: Full-time
- Work Mode: Hybrid
Open Positions / Department Details
- Position Title: Clinical Trial Associate I
- Department: Global Clinical Monitoring and Site Management
- Job Requisition ID: R5939
- Career Level: Entry-Level / Early Career
This role supports global clinical study teams and plays a key role in maintaining trial documentation quality and compliance. Clinical Trial Associate I Job
Key Roles & Responsibilities
Document Management Responsibilities
The Clinical Trial Associate I will actively support Trial Master File (TMF) and electronic TMF (eTMF) operations across the study lifecycle.
Key responsibilities include:
- Maintaining TMF and eTMF in alignment with sponsor SOPs and regulatory requirements
- Creating and managing TMF placeholders based on filing plans, milestones, document expiry, and site changes
- Reviewing essential site documents to ensure compliance with company, sponsor, regulatory, and ALCOA/ALCOAC principles
- Performing completeness and quality checks on assigned eTMF sections during study start-up, conduct, and close-out
- Following up with clinical teams to resolve TMF-related findings in a timely manner
- Generating and sharing eTMF status and quality reports with study teams
- Supporting CRAs and Site Start-Up Associates with essential document collection and review
- Assisting with document translations or review of translated site documents when required
Clinical Trial Associate I Job
Data Entry, Tracking, Reporting & System Support
The role involves extensive coordination and system-based support for clinical trial activities. Clinical Trial Associate I Job
Responsibilities include:
- Supporting CTMS setup and maintaining accurate data entries such as site contacts, addresses, assignments, and activation details
- Assisting in tracking distribution of Investigator’s Brochure, safety reports, and other study-related materials sent to sites
- Managing and monitoring system access for site staff and clinical teams across platforms such as CTMS, EDC, IWRS, and vendor portals
- Performing routine access reviews and supporting timely access removal
- Reviewing training matrices and compliance reports for clinical team members
- Supporting creation and management of CRA workflows to track site follow-up activities
Clinical Trial Associate I Job
Additional Clinical Support Activities
- Participating in internal clinical team meetings and supporting meeting documentation, action items, and follow-ups
- Coordinating with third-party vendors to resolve issues related to equipment, translations, or study materials
- Supporting study-level tracking tools such as Q&A logs and issue trackers
- Assisting in the preparation of Investigator Site Files and Pharmacy Files prior to Site Initiation Visits
- Coordinating with vendors for creation, review, and distribution of Investigator Site File binders
- Supporting general operational and logistical activities as assigned
- Participating in internal training programs to enhance therapeutic and clinical knowledge
- Performing additional duties aligned with clinical study support as required
Clinical Trial Associate I Job
Eligibility Criteria
Education
Candidates must possess:
- An undergraduate degree or international equivalent in:
- Life Sciences
- Nursing
- Medical Documentation
- Related healthcare or clinical research discipline
Experience
- Open to freshers and early-career professionals
- Prior clinical research experience is an advantage but not mandatory
Skills Required
- Strong verbal and written communication skills in English
- Basic understanding of clinical research processes
- Knowledge of ICH and GCP guidelines is preferred
- Proficiency in MS Word, Excel, PowerPoint, and Outlook
- Strong organizational and documentation skills
- Good interpersonal, coordination, and listening abilities
- Ability to work collaboratively in a global clinical team environment
Salary & Benefits
- Salary: As per company norms
Additional benefits include:
- Full-time stable employment
- Hybrid work flexibility
- Exposure to global clinical trial operations
- Structured learning and skill development opportunities
- Supportive and inclusive work culture
- Career growth within clinical operations and site management
Selection Process
The selection process may include:
- Application screening
- Interview with clinical operations team
- Final HR discussion
Shortlisted candidates will be contacted directly by the employer.
How to Apply
- Mode of Application: Online Application
Interested candidates must apply through the official application link provided by the employer.
Important Dates
- Last Date to Apply: February 7, 2026
Candidates are encouraged to apply promptly as the application window is short. Clinical Trial Associate I Job
Why Apply for This Pharma Job?
This role offers an excellent entry point into global clinical trial operations. Candidates gain real-time exposure to TMF management, CTMS systems, regulatory compliance, and cross-functional collaboration. The hybrid work model, combined with structured training and mentorship, makes this position ideal for professionals looking to build a strong foundation in clinical research. Clinical Trial Associate I Job
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent pharma job information platform and is not affiliated with Premier Research or any organization. Job details are shared for informational purposes only. Applicants should verify all information through official employer communication before applying. Clinical Trial Associate I Job
Final Call-to-Action
If you are ready to begin your career in clinical trial operations and work on global studies, apply now without delay. Clinical Trial Associate I Job
