Premier Research Hiring Clinical Trial Associate Job in Bangalore for life sciences graduates with clinical research experience.
Introduction
Clinical research organizations play a crucial role in bringing innovative medicines, medical devices, and diagnostics to patients around the world. These organizations support pharmaceutical and biotechnology companies by managing clinical trials, ensuring regulatory compliance, and maintaining high-quality research documentation.
Premier Research is currently inviting applications for the position of Clinical Trial Associate II (CTA II) as part of its Global Clinical Monitoring and Site Management team. This hybrid role based in Bangalore, India, offers a great opportunity for professionals with clinical research experience to contribute to global clinical trials and support the development of life-saving treatments. Premier Research Hiring Clinical Trial Associate Job
Company Overview
Premier Research is a global clinical research organization that partners with biotechnology, medical device, and specialty pharmaceutical companies. The organization focuses on supporting innovative healthcare solutions by managing clinical development programs and ensuring that new therapies reach patients efficiently and safely.
The company is known for its collaborative work culture and commitment to scientific innovation. Premier Research works closely with sponsors, investigators, and clinical teams worldwide to conduct high-quality clinical trials while maintaining strict compliance with regulatory guidelines. Premier Research Hiring Clinical Trial Associate Job
Job Location & Employment Type
| Job Detail | Information |
|---|---|
| Company | Premier Research |
| Job Role | Clinical Trial Associate II |
| Department | Global Clinical Monitoring & Site Management |
| Location | Bangalore, India |
| Work Model | Hybrid |
| Employment Type | Full-Time |
| Industry | Clinical Research / Pharmaceutical |
| Job Requisition ID | R5940 |
| Application Mode | Online Application |
Department Overview
The Clinical Trial Associate II role is part of the clinical monitoring and site management operations team. This team is responsible for supporting clinical trials by maintaining regulatory documentation, managing trial master files, coordinating with clinical teams, and ensuring compliance with international clinical research standards.
The selected candidate will collaborate with clinical research associates (CRAs), study teams, and external vendors to maintain documentation accuracy, monitor trial progress, and ensure regulatory compliance across clinical trial activities. Premier Research Hiring Clinical Trial Associate Job
Key Roles & Responsibilities
Trial Master File Management
- Maintain the Trial Master File (TMF) or electronic Trial Master File (eTMF) in accordance with company and sponsor procedures.
- Ensure documentation is properly filed according to trial master file filing plans.
- Create and maintain placeholders for expired documents, study milestones, or changes in site staff.
Documentation Review & Compliance
- Review site documents to ensure compliance with regulatory standards and company procedures.
- Perform quality reviews and completeness checks of eTMF sections during trial start-up, maintenance, and close-out phases.
- Ensure documentation follows ALCOA+ principles and ICH-GCP requirements.
Clinical Team Coordination
- Follow up with internal teams to resolve TMF queries and ensure timely document updates.
- Assist Clinical Research Associates (CRAs) with the collection and review of essential documents from study sites.
- Support translation and verification of site documents when required.
Data Management & Tracking
- Assist with Clinical Trial Management System (CTMS) setup and data entry for project tracking activities.
- Maintain accurate records of site contact details, site assignments, and activation activities.
- Track distribution of investigator brochures, safety reports, and other study materials.
System Access Management
- Manage access to research systems including CTMS, vendor systems, EDC, and IWRS platforms.
- Conduct routine checks to ensure system access permissions remain accurate and up to date.
Reporting & Documentation
- Generate eTMF reports for clinical teams to monitor documentation quality and compliance.
- Assist with project tracking reports and training compliance monitoring.
- Maintain logs and documentation related to study operations.
Operational & Administrative Support
- Attend internal clinical team meetings and assist with meeting preparation and follow-up actions.
- Support coordination with third-party vendors related to equipment, documentation, or translation activities.
- Assist with the preparation of Investigator Site Files (ISF) before site initiation visits.
- Manage logistical tasks related to study documentation and project activities.
Team Support & Development
- Participate in internal training programs to enhance therapeutic knowledge.
- Support less experienced Clinical Trial Associates through mentoring or training when required.
- Act as a contact point for IT-related issues affecting project systems.
Premier Research Hiring Clinical Trial Associate Job
Eligibility Criteria
Education
Candidates should possess:
- Bachelor’s degree in Life Sciences, Nursing, Medical Documentation, or related field
- Equivalent international qualifications may also be considered.
Experience
- Minimum 1 year of experience as a Clinical Trial Associate or similar clinical research role.
- Combination of education and relevant work experience may also be considered.
Skills Required
- Knowledge of ICH-GCP guidelines and clinical research documentation requirements.
- Understanding of essential clinical trial documents and ALCOA+ data integrity principles.
- Experience using clinical research systems such as CTMS or eTMF platforms.
- Strong computer skills including Microsoft Word, Excel, PowerPoint, and Outlook.
- Excellent interpersonal and communication skills.
- Strong organizational and time management abilities.
- Ability to manage multiple tasks while meeting deadlines.
- Capability to work independently as well as collaboratively within a team environment.
Salary & Benefits
Compensation and benefits will be provided as per company norms and may vary depending on the candidate’s experience and qualifications. Premier Research Hiring Clinical Trial Associate Job
Employees working with global clinical research organizations often receive additional benefits such as:
- Competitive salary packages
- Professional development opportunities
- Exposure to global clinical research projects
- Work-life balance initiatives
- Collaborative and inclusive work environment
Selection Process
The recruitment process may include the following stages:
- Resume Screening
- HR Interview
- Technical Interview with Clinical Research Team
- Final Selection
Shortlisted candidates will be contacted by the recruitment team for further evaluation. Premier Research Hiring Clinical Trial Associate Job
How to Apply
Interested candidates who meet the eligibility requirements can apply through Premier Research’s official careers portal. Applicants should ensure that their resumes highlight relevant clinical research experience, documentation management skills, and knowledge of regulatory guidelines. Premier Research Hiring Clinical Trial Associate Job
Important Dates
| Event | Date |
|---|---|
| Application Deadline | March 17, 2026 |
Since the application deadline is approaching soon, candidates are advised to submit their applications immediately. Premier Research Hiring Clinical Trial Associate Job
Why Apply for This Pharma Job?
Clinical research roles such as Clinical Trial Associate provide valuable exposure to the drug development process. Professionals in these roles support global clinical trials by managing documentation, coordinating study activities, and ensuring compliance with regulatory standards.
This opportunity at Premier Research allows candidates to work with international clinical teams and contribute to research programs that help bring innovative treatments to patients. For professionals interested in building long-term careers in clinical research, clinical operations, or regulatory documentation, this role provides excellent industry experience. Premier Research Hiring Clinical Trial Associate Job
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform that publishes pharmaceutical and life sciences job updates for informational purposes only. We are not affiliated with Premier Research or any company mentioned in this job post. Candidates should verify job details from the official company website before applying. IndiaPharmaJobs.in does not charge any fee for job information. Premier Research Hiring Clinical Trial Associate Job
Final Call-to-Action
Clinical research professionals with experience in clinical trial documentation and regulatory compliance should consider applying for this opportunity at Premier Research. If you meet the eligibility criteria and want to contribute to global clinical development programs, submit your application before the deadline for the Clinical Trial Associate II position in Bangalore. Premier Research Hiring Clinical Trial Associate Job
