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Centralized Study Spec I

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Onsite

Centralized Study Spec I

Fortrea

Centralized Study Spec I

Skills

Google Cloud PlatformWorkdayProcess ImprovementCompliance

1 month ago

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Important information


Contract type:

Permanent

Location:

Bengaluru, Karnataka, India

Work mode:

Onsite

Published on:

24 September 2026

What they need


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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