Site Activation Specialist Position at Fortrea | Apply Now
A rare chance has emerged for professionals in clinical development and research. Fortrea is seeking a Study Start-up Associate (Site Activation Specialist) for a full-time remote opportunity based in Bangalore and Mumbai. Candidates with a life-science degree and at least 2 years of relevant experience are encouraged to apply by 30 September 2026.
About The Company
Fortrea is a prominent organization in the clinical research field, specializing in providing comprehensive solutions for clinical trials. With a commitment to advancing healthcare through innovative research, Fortrea operates in various locations, including Bangalore and Mumbai. The company focuses on ensuring that clinical studies are conducted efficiently, adhering to regulatory standards and ethical guidelines.
- Position: Study Start-up Associate (Site Activation Specialist)
- Work Type: Remote
- Location: Bangalore, Mumbai
- Experience: Minimum 2 years
- Education: University/College degree preferred in Life Sciences
- Job ID: 264943
- Last Date to Apply: 30 September 2026
Clinical Study Start-up Position: Job Description
The Study Start-up Associate plays a crucial role in facilitating the transition of clinical trials from initiation to site activation. This position serves as a key point of contact among investigative sites, sponsors, regulatory authorities, ethics committees, and internal teams. The professional must possess a strong understanding of ICH/GCP guidelines, regulatory requirements, and clinical trial submissions.
Key Responsibilities
- Coordinating with investigative sites during study start-up and maintenance activities.
- Collecting and tracking investigator and essential study documents.
- Preparing documentation for EC/IRB/IEC and Regulatory Authority submissions.
- Compiling routine regulatory submissions, including INDs and CTAs, where applicable.
- Liaising with Regulatory Authorities and ethics committees regarding submissions and approvals.
- Ensuring study start-up activities align with timelines, budgets, SOPs, and applicable regulations.
- Performing quality reviews and ensuring study documentation is appropriately filed.
- Supporting site activation strategy and providing timelines and projections.
Clinical Study Start-up Position: Eligibility Criteria
- University or college degree, preferably in Life Sciences.
- Minimum 2 years of experience in clinical research, clinical development, site start-up, or regulatory processes.
- Strong working knowledge of ICH guidelines and understanding of Regulatory Authority and IRB/IEC requirements.
- Experience interacting with investigative sites and operational project teams.
Fortrea Study Start-Up Associate: Required Skills
- Clinical Research
- Regulatory Affairs
- ICH-GCP
- Essential Document Management
- Clinical Trial Documentation
- Risk Identification and Escalation
- Contract and Budget Coordination
- Regulatory Compliance
Salary and Benefits: The job description does not specify a salary or detailed employee benefits package. However, a reasonable market estimate for a Study Start-up professional with around 2+ years of relevant experience in India could be approximately ₹5 lakh–₹9 lakh per annum, depending on experience, location, skills, and compensation structure.
This opportunity at Fortrea represents a significant step for qualified candidates looking to advance their careers in clinical research. This clinical study start-up position may suit professionals seeking site-activation experience. Interested individuals are encouraged to apply before the deadline of 30 September 2026 to seize this opportunity.
