Centralized Study Specialist II at Fortrea, Bangalore
A rare chance has emerged for qualified candidates to join Fortrea as a Centralized Study Specialist II in Bangalore. This role requires 3 to 5 years of experience in clinical research and offers an opportunity to contribute to vital clinical trial processes. Interested applicants should apply by 30 September 2026.
About Fortrea
Fortrea is a prominent organization in the pharmaceutical sector, dedicated to advancing clinical research and development. With a focus on improving patient outcomes, Fortrea operates globally, providing innovative solutions and support for clinical trials. The company is committed to maintaining high standards of quality and compliance in all its operations.
Company: Fortrea
Location: Bangalore, India
Experience: 3–5 years of work experience in clinical research
Qualification: University/College Degree (Life Science preferred), or certification in an allied health profession from an appropriate accredited institution
Job Reference: 264666
Application Start Date: 14 August 2026
Application Deadline: 30 September 2026
Centralized Study Specialist II Job Description
The Centralized Study Specialist II will be responsible for drafting, reviewing, negotiating, and finalizing Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation. The role involves coordinating with sponsors, legal teams, clinical operations, and study teams to facilitate timely contract execution and managing site agreement timelines.
Key Responsibilities
- Draft, review, negotiate, and finalize CTAs and related documentation.
- Coordinate with relevant teams to ensure timely contract execution.
- Maintain accurate contract status updates and documentation in relevant systems.
- Facilitate internal approval workflows and obtain required authorizations.
- Track contract execution status and ensure proper filing of executed documents.
- Identify contracting risks and escalate issues to management as needed.
- Support protocol amendment submissions and related documentation updates.
- Ensure adherence to SOPs, sponsor requirements, and ICH-GCP principles.
Eligibility Criteria
- University/College Degree (Life Science preferred) or relevant certification.
- 3–5 years of work experience in clinical research.
- Strong understanding of ICH-GCP guidelines and clinical research operations.
Required Skills
- Excellent communication and negotiation skills.
- Strong organizational and multitasking abilities.
- Proficiency in contract tracking systems and Microsoft Office applications.
- Ability to manage multiple studies and priorities within tight timelines.
How to Apply
Interested candidates can apply through the official Fortrea Workday portal: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE.
Conclusion
This Centralized Study Specialist II opportunity is an excellent option for qualified individuals looking to advance their careers at Fortrea. Candidates with the required experience and skills are encouraged to apply before the deadline of 30 September 2026.
