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Salary
≈ $15k – $31k per year (Estimated)
Location
In office (Bengaluru)
Seniority
Middle · 3+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 14, 2026. First seen by Alion on Sep 24, 2026.

Overview
Company
Impact
Profile match
Fortrea is an American contract research organisation that provides clinical development services to pharmaceutical, biotechnology and medical device companies. It runs Phase I to IV clinical trials, offers functional service provider staffing and patient access solutions, and operates in about 90 countries. The company was spun off from Labcorp in 2023 and is headquartered in Durham, North Carolina, United States.

Summary of Responsibilities:

  • Review and implementation of relevant study-specific plans that describe the required expectations for assigned tasks
  • Support system compliance and system data entry, as applicable
  • File required task-related documentation in the Electronic Trial Master File (eTMF)
  • Review initial/amended Country/Site ICFs in compliance with Sponsor requirements, local regulatory requirements and Good Clinical Practice (GCP) guidelines.
  • Liaising and follow-up with local teams, Start-up Project Managers, and Sponsors to assure timely approval of Informed Consent Forms in order to meet submission deadlines.

To follow all applicable departmental Standard Operating Procedures and Work Instructions:

  • To complete required trainings according to required timelines.
  • To complete day-to-day tasks ensuring quality and productivity.
  • To manage project and technical documentation in an appropriate manner.
  • To provide administrative and technical support to internal departments and teams as needed.
  • To perform checks to ensure quality of work completed.
  • To ensure timely escalation and issue resolution as needed.
  • To participate in process improvement opportunities and assist with the implementation of revised processes and procedures.
  • All other duties as needed or assigned.

Qualifications (Minimum Required):

  • University/College degree (life science preferred), or certification in a related 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

Experience (Minimum Required):

  • Working knowledge of ICH, FDA, IRB/IEC and other applicable regulations/guidelines.
  • 3-5 years' work experience in clinical research
  • Previous interaction with operational project teams preferred.

Preferred Qualifications Include:

  • Computer proficiency in MS Office (Word, Excel, PowerPoint, Access, Outlook e-mail and internet services)
  • Good written and oral communication skills
  • Well-developed organizational skills
  • Excellent proof-reading skills

Physical Demands/Work Environment:

  • General Office Environment.

Learn more about our EEO & Accommodations request here.

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