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 Setting:

- General Office Environment.

Learn more about our EEO & Accommodations request here .

📌 Centralized Study Spec I (India)
🏢 Fortrea
📍 India