Clinical Trial Associate II at Premier Research (Apply by June 5, 2025)
Premier Research is actively seeking a Clinical Trial Associate II to join its Global Clinical Monitoring and Site Management team in a hybrid role based in Bangalore, India. This is a full-time opportunity ideal for professionals who want to make a meaningful impact in clinical research, working with a company that partners with biotech, medtech, and specialty pharma companies worldwide.
If you are passionate about supporting life-changing therapies and eager to be part of an organization that values flexibility, innovation, and personal growth—this role could be a perfect match.
Position: Clinical Trial Associate II
Location: Bangalore, India (Hybrid)
Job Type: Full-time
Application Deadline: June 5, 2025
Job Requisition ID: R4632
About Premier Research
Premier Research is built around people—employees, clients, and most importantly, patients. The organization helps turn breakthrough science into new medical solutions, and it takes pride in offering a collaborative and flexible environment where each team member can grow professionally while contributing to real-world innovations.
Key Responsibilities
1. Document Management
Maintain and update the Trial Master File (TMF) and electronic TMF (eTMF) in line with company and regulatory requirements.
Perform quality control checks and reviews of essential documents.
Collaborate with the clinical team on document queries, placeholder creation, and follow-ups.
Assist with translation and verification of site documents when necessary.
2. Data Entry and System Tracking
Support setup and updates in Clinical Trial Management Systems (CTMS).
Track and document safety reports, newsletters, and Investigator's Brochures sent to sites.
Maintain access logs for systems such as CTMS, EDC, IWRS, and vendor platforms.
Monitor training compliance and assist in workflow creation for CRAs.
3. Study Support and Coordination
Prepare for and follow up on internal meetings, documenting actions and issues.
Coordinate with third-party vendors on study-related issues such as equipment or translations.
Support the development and distribution of site materials like Investigator Site Files.
Participate in training programs to enhance therapeutic and technical knowledge.
4. Additional Duties
Provide logistical support for clinical activities.
Mentor junior CTAs where applicable.
Help resolve IT issues related to study documentation and systems.
Escalate issues and collaborate on effective solutions.
Engage in departmental improvement initiatives.
Qualifications
Prior experience in clinical trial operations, particularly in document management and system tracking.
Strong understanding of Good Clinical Practice (GCP), TMF structure, and clinical systems.
Excellent communication, organizational, and time management skills.
Ability to work independently while contributing to a team environment.
Why Work at Premier Research?
A workplace that values flexibility, career development, and innovation.
Opportunities to contribute directly to the development of new treatments and technologies.
A collaborative team environment with global reach and resources.
Training and mentoring programs to help you grow your career in clinical research.
How to Apply
To apply, search for Requisition ID R4632 on the Premier Research careers page or visit
https://premierresearch.wd12.myworkdayjobs.com/PremierResearch/job/Bangalore-India/Clinical-Trial-Associate-II_R4632
Make sure to apply before June 5, 2025.
Take the next step in your clinical research journey with Premier Research—where your work has the power to improve lives across the globe.
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