Fortrea Regulatory and Start-Up Job in Bangalore, India (2026)

Fortrea is hiring Regulatory and Start-Up professionals in Bangalore, India, for Clinical Trial Agreements and site start-up contracting. Candidates need 3–5 years of clinical research experience and a relevant degree or allied health certification.

Job Details

Company: Fortrea

Job Title: REGULATORY AND START-UP

Location: Bangalore, India

Workday Job ID: 262931

Date Posted: 04 November 2026

Environment: General office

Job Description

Fortrea is hiring for REGULATORY AND START-UP (Clinical Trial Agreements / site start-up contracting) in Bangalore.

Key Responsibilities

  • Draft, review, negotiate and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments and related site contract documentation.
  • Coordinate with sponsors, legal teams, clinical operations and study teams to facilitate timely contract execution.
  • Manage site agreement timelines and ensure contracts are completed within study milestones and agreed turnaround timelines.
  • Maintain accurate contract status updates and documentation in SAMS, UCV and other applicable systems.
  • Facilitate internal approval workflows and obtain required authorizations for agreement execution.
  • Track contract execution status and ensure executed documents are filed appropriately.
  • Identify contracting risks, delays and issues proactively and escalate where required.
  • Provide regular updates to study teams and management.
  • Coordinate protocol amendment submissions and associated documentation updates for assigned studies and sites.
  • Support amendment-related contract and budget revisions in alignment with approved protocol changes.
  • Review amendment requirements and communicate action items, timelines and documentation needs to sites and study teams.
  • Track amendment progress and ensure timely completion of submissions, approvals and implementation activities.
  • Collaborate with Clinical Operations, Regulatory, Legal and Finance.
  • Ensure adherence to SOPs, sponsor requirements, quality standards and ICH-GCP.
  • Maintain accurate study trackers, reports and metrics.
  • Support audit readiness.
  • Participate in process improvement initiatives.
  • Complete assigned training, timesheets and compliance activities within required timelines.

Eligibility Criteria

Experience: 03–05 years of work experience in clinical research / the job discipline, including strong working knowledge of ICH-GCP and applicable guidelines and regulations. Also listed: 00–02 years of experience in other professional roles. Freshers not eligible for the 3–5 year clinical-research minimum.

Qualification: University/College Degree (Life Science preferred), or certification in an allied health profession from an appropriate accredited institution (e.g. nursing certification, medical or laboratory technology). Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Required Skills

  • Strong understanding of clinical trial contracting and protocol amendment processes.
  • Knowledge of ICH-GCP and clinical research operations.
  • Excellent communication, negotiation and stakeholder management.
  • 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.

How to Apply

Official apply link is the Fortrea Workday REGULATORY AND START-UP posting 262931.

CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

Apply through the official Fortrea Workday posting 262931.