Life Science Jobs at Fortrea | Clinical Research Role | Candidates Apply Now
Are you looking for Life Science Jobs or Clinical Research Jobs in Bangalore? Here’s an exciting opportunity through Fortrea Careers for the position of Centralized Study Analyst. If you have experience in clinical trial contracting, protocol amendments, ICH-GCP guidelines, and study management, this role offers a great opportunity to advance your career in clinical research while working with a globally recognized organization.
About Fortrea
Fortrea is a leading global contract research organization (CRO) providing clinical development, patient access, and technology solutions to pharmaceutical, biotechnology, and medical device companies worldwide. Through Fortrea Careers, professionals gain opportunities to work on innovative clinical research projects while contributing to advancements in healthcare and life sciences. The company is known for its expertise in clinical operations, regulatory support, and end-to-end clinical trial management.
Job Overview
- Position: Centralized Study Analyst
- Location: Bangalore
- Job Type: Full Time
- Work Mode: Hybrid
- Application Deadline: June 30, 2026
- Experience Required: 3-5 Years
This opportunity under Fortrea Careers is ideal for professionals seeking Life Science Jobs and Clinical Research Jobs involving clinical trial contracting, protocol amendment management, and study operations support.
Key Responsibilities
- Manage Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and site contract documentation from drafting to execution.
- Coordinate with sponsors, legal, regulatory, finance, and clinical operations teams to ensure timely contract execution and protocol amendment implementation.
- Track contract and amendment progress, maintain accurate documentation in applicable systems, and ensure compliance with SOPs, sponsor requirements, and ICH-GCP guidelines.
- Identify risks, provide study status updates, support audit readiness, and collaborate with stakeholders to ensure efficient study execution and milestone achievement.
Qualifications
- University/College Degree (Life Science preferred), or certification in an allied health profession from an appropriate accredited institution. Examples include Nursing certification, Medical Technology, or Laboratory Technology.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Experience Required
- 03-05 years of work experience in clinical research.
- Strong working knowledge of ICH-GCP guidelines and all applicable regulations.
- 03-05 years of experience in the job discipline.
- 00-02 years of experience in other professional roles.
Skills Needed
- Strong understanding of clinical trial contracting and protocol amendment processes.
- Knowledge of ICH-GCP guidelines and clinical research operations.
- Excellent communication, negotiation, and stakeholder management skills.
- Strong organizational and multitasking abilities with attention to detail.
- Ability to manage multiple studies and priorities within tight timelines.
- Proficiency in contract tracking systems and Microsoft Office applications.
- Demonstrated ability to organize and communicate effectively.
- Demonstrated ability to pay attention to detail.
- Ability to work well with others.
- Ability to deliver consistent high-quality work.
- Ability to use a computer and departmental tools.
Work Environment
- General Office Environment.
- Hybrid working model based in Bangalore.
Professionals searching for Life Science Jobs, Clinical Research Jobs, and opportunities through Fortrea Careers can explore this Centralized Study Analyst position in Bangalore. With responsibilities spanning clinical trial agreements, protocol amendments, regulatory compliance, and stakeholder coordination, this role offers an excellent opportunity for experienced clinical research professionals to advance their careers in a dynamic and globally recognized organization.
