Fortrea Hiring Centralized Study Analyst

Fortrea Hiring Centralized Study Analyst | Clinical Research Jobs in Bangalore

Fortrea is hiring experienced clinical research professionals for the position of Centralized Study Analyst in Bangalore. This hybrid opportunity is ideal for candidates with experience in clinical trial agreements, site contracting, protocol amendment coordination, clinical operations, and study management.

Candidates with backgrounds in life sciences, pharmacy, nursing, biotechnology, medical laboratory technology, and clinical research can apply for this opportunity.

The role offers exposure to global clinical trial operations, site management processes, contract negotiation, regulatory coordination, and sponsor communication within an international CRO environment.

Professionals searching for clinical research jobs in Bangalore, CTA specialist jobs, clinical trial agreement careers, protocol amendment jobs, CRO operations roles, and clinical operations analyst positions may find this opportunity highly relevant.

Company Overview

Fortrea is a global Contract Research Organization (CRO) providing clinical development, patient access, and technology solutions to pharmaceutical, biotechnology, and medical device companies.

The company supports clinical trials across multiple therapeutic areas and regulated global markets.

Fortrea professionals work across:

• Clinical operations
• Site management
• Clinical trial contracting
• Regulatory coordination
• Pharmacovigilance
• Medical affairs
• Clinical data management
• Study startup operations

The organization is known for:

• Global clinical research projects
• Hybrid working opportunities
• CRO career growth
• Regulatory compliance systems
• International clinical trial operations
• Collaborative work culture

Employees gain experience in sponsor communication, protocol management, site contracting, and global clinical research workflows.

Job Role & Responsibilities

Position Available

• Centralized Study Analyst

Clinical Trial Agreement Responsibilities

Selected candidates will:

• Draft Clinical Trial Agreements (CTAs)
• Review and negotiate study contracts
• Finalize confidentiality agreements
• Handle site contract documentation
• Coordinate agreement execution activities
• Support legal and sponsor communications

Contract & Site Coordination

Candidates will:

• Coordinate with clinical operations teams
• Support study startup activities
• Track agreement timelines
• Ensure milestone-based contract completion
• Maintain contract status updates
• Handle internal approval workflows
• Maintain executed agreement records

Protocol Amendment Coordination

Responsibilities include:

• Coordinating protocol amendment submissions
• Managing documentation updates
• Supporting contract and budget revisions
• Communicating amendment timelines to sites
• Tracking amendment approvals and implementation
• Coordinating cross-functional amendment activities

Stakeholder Management

The role requires coordination with:

• Clinical Operations teams
• Regulatory Affairs teams
• Legal departments
• Finance teams
• Study teams
• Sponsors
• Investigative sites

Compliance & Documentation Responsibilities

Candidates will ensure:

• SOP compliance
• ICH-GCP adherence
• Accurate study tracking
• Audit-ready documentation
• Timely escalation of risks
• Maintenance of study reports and metrics

Operational Responsibilities

Selected professionals may also:

• Support process improvement initiatives
• Participate in operational reviews
• Maintain study trackers
• Complete compliance activities
• Manage multiple studies simultaneously

This role is highly relevant for candidates searching for:

• Clinical trial agreement jobs
• Clinical operations analyst roles
• Site contracting jobs
• Clinical research coordinator careers
• CRO jobs in Bangalore
• Protocol amendment specialist roles
• Study startup jobs
• CTA analyst careers

Eligibility / Qualifications

Educational Qualification

Candidates with the following qualifications can apply:

• Life Sciences Degree
• Pharmacy
• Biotechnology
• Nursing
• Medical Laboratory Technology
• Allied Health Sciences
• Clinical Research-related education

Experience Required

• 3 to 5 years of clinical research experience

Preferred experience includes:

• Clinical trial contracting
• Site management
• Protocol amendment handling
• CRO operations
• Study startup coordination
• Clinical operations support

Required Skills

Candidates should possess:

• Knowledge of ICH-GCP guidelines
• Clinical trial agreement experience
• Contract negotiation skills
• Stakeholder communication abilities
• Attention to detail
• Multi-tasking capabilities
• Documentation management expertise
• Microsoft Office proficiency

Preferred Competencies

• Risk identification skills
• Clinical research operations knowledge
• Cross-functional coordination experience
• Contract tracking system knowledge
• Strong organizational skills

Location & Salary

Job Location

• Bangalore

Work Mode

• Hybrid

Expected Salary

Based on current CRO and clinical research industry standards in India, professionals in clinical trial contracting and study analyst roles generally receive:

• ₹6 LPA to ₹11 LPA

Salary may vary depending on:

• CRO experience
• Clinical operations expertise
• Site contracting knowledge
• Protocol amendment exposure
• Sponsor management experience

Application Process

Interested candidates can apply online through the official Fortrea careers portal.

Apply Link

https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Centralized-Study-Analyst_262483

Job Information

• Position: Centralized Study Analyst
• Company: Fortrea
• Job Requisition ID: 262483
• Work Mode: Hybrid
• Location: Bangalore

Important Instructions

Candidates should:

• Update their latest resume
• Highlight CTA and site contracting experience
• Mention protocol amendment handling experience clearly
• Include CRO and clinical operations exposure
• Showcase ICH-GCP knowledge
• Mention stakeholder management experience

Frequently Asked Questions (FAQs)

1. Which company is hiring for this role?

Fortrea is hiring for the Centralized Study Analyst position.

2. What experience is required?

Candidates should have 3–5 years of clinical research experience.

3. Is this a remote role?

No. This is a hybrid role based in Bangalore.

4. Which qualifications are eligible?

Life Sciences, Pharmacy, Biotechnology, Nursing, and Allied Health candidates can apply.

5. What type of work will candidates handle?

Candidates will handle CTAs, protocol amendments, site contracts, study coordination, and sponsor communication.

6. What is the expected salary range?

The estimated salary range is approximately ₹6 LPA to ₹11 LPA.

Summary

Company	Fortrea
Department Vacancies	Centralized Study Analyst
Qualification	Life Sciences / Pharmacy / Biotechnology / Nursing
Experience	3–5 Years
Location	Bangalore

Tagged as: Pharma Jobs in Bangalore