Fortrea is hiring for a Regulatory and Start-Up position in Bangalore. This is a full-time opportunity for clinical research professionals with experience in clinical trial contracting, regulatory coordination, and study start-up activities.
The role involves managing Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, site documentation, contract timelines, and related study start-up activities. The selected candidate will coordinate with sponsors, legal teams, clinical operations, regulatory teams, finance, study teams, and sites to support timely study execution.
Candidates with a university or college degree, preferably in Life Sciences, along with 3–5 years of relevant clinical research experience, can apply. A strong understanding of ICH-GCP guidelines and clinical research operations is required.
Fortrea Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Fortrea |
| Position | Regulatory and Start-Up |
| Job Requisition ID | 262931 |
| Location | Bangalore |
| Job Type | Full Time |
| Experience | 3–5 Years |
| Qualification | University / College Degree |
| Preferred Background | Life Sciences |
| Key Area | Clinical Research / Regulatory / Study Start-Up |
| Work Environment | General Office Environment |
| Application Deadline | 30 October 2026 |
About Fortrea
Fortrea is a clinical research organization supporting clinical development programs and research activities within the life sciences industry.
The Regulatory and Start-Up role supports the operational requirements involved in getting clinical studies and sites ready, including contract execution, protocol amendment coordination, documentation, tracking, stakeholder communication, and compliance activities.
Job Description
The Regulatory and Start-Up professional will be responsible for supporting clinical trial contracting and protocol amendment activities for assigned studies and sites.
The role requires close coordination with sponsors, sites, legal teams, clinical operations, regulatory teams, finance, and other stakeholders. The candidate will monitor timelines, maintain accurate records, identify potential delays, and escalate issues that could affect study milestones.
The position also contributes to audit readiness, compliance activities, reporting, and process improvement initiatives.
Eligibility Criteria
Candidates should meet the following requirements:
- University or college degree, preferably in Life Sciences.
- Certification in an allied health profession from an appropriately accredited institution may also be considered, such as nursing or medical/laboratory technology certification.
- 3–5 years of work experience in clinical research.
- Strong working knowledge of ICH-GCP guidelines and other applicable guidelines and regulations.
- Ability to organize work effectively and communicate with different stakeholders.
- Strong attention to detail.
- Ability to work effectively with others.
- Ability to consistently deliver high-quality work.
- Ability to use computers and relevant departmental tools.
Fortrea may consider relevant and equivalent professional experience in place of the stated educational requirements.
Skills and Qualifications
Candidates should have the following skills and competencies:
- Understanding of clinical trial contracting processes.
- Knowledge of Clinical Trial Agreements and related site documentation.
- Understanding of protocol amendment processes.
- Knowledge of ICH-GCP principles.
- Familiarity with clinical research operations.
- Strong communication skills.
- Negotiation and stakeholder-management abilities.
- Strong organizational and multitasking skills.
- Excellent attention to detail.
- Ability to manage multiple studies and competing priorities.
- Ability to work within strict timelines.
- Proficiency with contract tracking systems.
- Working knowledge of Microsoft Office applications.
- Ability to identify and communicate risks, delays, and operational issues.
Key Responsibilities
The selected candidate will support activities including:
Clinical Trial Contracting
- Draft, review, negotiate, and finalize Clinical Trial Agreements and confidentiality agreements.
- Manage amendments and other site contract documentation.
- Coordinate with sponsors, legal teams, clinical operations, and study teams to support timely contract execution.
- Monitor site agreement timelines against study milestones and agreed turnaround times.
- Maintain accurate contract status information in SAMS, UCV, and other applicable systems.
- Facilitate internal approval workflows and obtain necessary authorizations.
- Track execution of agreements and ensure completed documents are appropriately filed.
- Identify contracting risks, delays, and issues and escalate them when required.
- Provide regular contract-status updates to study teams and management.
Protocol Amendment Coordination
- Coordinate protocol amendment submissions and related documentation updates for assigned studies and sites.
- Support contract and budget revisions associated with approved protocol changes.
- Review amendment requirements and communicate action items and timelines to relevant stakeholders.
- Inform sites and study teams about required documentation and implementation activities.
- Track amendment submissions, approvals, and implementation progress.
- Coordinate with Clinical Operations, Regulatory, Legal, Finance, and other relevant teams.
- Ensure amendment-related documentation is accurately maintained in applicable systems and trackers.
- Follow up with sites regarding outstanding questions or documentation requirements.
- Help prevent delays in amendment implementation through timely communication and tracking.
Compliance and Study Support
- Follow applicable SOPs, sponsor requirements, quality standards, and ICH-GCP principles.
- Maintain accurate study trackers, reports, and operational metrics.
- Escalate risks, delays, and operational challenges that could affect study deliverables.
- Support audit readiness by maintaining complete and accurate documentation.
- Participate in process improvement activities.
- Collaborate with internal and external stakeholders to support efficient study execution.
- Complete required training, timesheets, and compliance-related activities within specified timelines.
Work Location and Environment
The position is based in Bangalore and is offered as a full-time role.
The job posting specifies a general office environment.
Salary / CTC
Fortrea has not specified the salary or CTC for this position in the provided job posting. Candidates should refer to official recruitment communication for compensation-related information.
Selection Process
The detailed selection process has not been specified in the supplied vacancy information. Candidates who meet the requirements can submit their application through the official Fortrea careers portal and follow any further instructions provided during the hiring process.
How to Apply for Fortrea Recruitment 2026
Eligible candidates can apply online through the official Fortrea careers portal.
Position: Regulatory and Start-Up
Job Requisition ID: 262931
Location: Bangalore
Job Type: Full Time
Application Deadline: 30 October 2026
Candidates should carefully review the eligibility requirements and ensure that all information submitted in the application is accurate and complete.
Important Details Before Applying
- Company: Fortrea
- Position: Regulatory and Start-Up
- Requisition ID: 262931
- Location: Bangalore
- Job Type: Full Time
- Experience: 3–5 Years in Clinical Research
- Qualification: University / College Degree
- Preferred Qualification: Life Sciences
- Key Knowledge: ICH-GCP and Clinical Research Operations
- Work Environment: General Office Environment
- Application Deadline: 30 October 2026
- Application Mode: Online
Important Note
Candidates should verify their educational qualifications, clinical research experience, and knowledge of applicable guidelines before applying. Job availability, application deadlines, eligibility requirements, and recruitment conditions may change. Applicants are advised to check the latest information on the official Fortrea careers portal before submitting their application.
FAQs – Fortrea Recruitment 2026
1. What position is Fortrea hiring for?
Fortrea is hiring for a Regulatory and Start-Up position.
2. Where is this Fortrea job located?
The position is based in Bangalore.
3. What qualification is required?
A university or college degree, preferably in Life Sciences, is required. An appropriate allied health certification may also be considered.
4. How much experience is required?
Candidates should have 3–5 years of clinical research experience, with relevant experience in the job discipline.
5. What knowledge is required for this role?
Candidates should have a strong working knowledge of ICH-GCP guidelines and applicable clinical research guidelines and regulations.
6. What are the main responsibilities of this position?
The role covers Clinical Trial Agreement management, contract coordination, protocol amendment activities, documentation, tracking, stakeholder communication, compliance, audit readiness, and study start-up support.
7. What is the application deadline?
The listed application deadline is 30 October 2026.
This version keeps the contracting, amendment, ICH-GCP, experience, qualification, location, and deadline details aligned with the supplied Fortrea posting.