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Entry Level Job in Clinical Studies | Fortrea
Overview
Position Name: Site Readiness and Regulatory Specialist 1
Organization: Fortrea
Qualification: B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences
Experience: 1 to 2 Years
Salary: Not disclosed
Location: Bangalore
About Us: Fortrea, a global contract research organization (CRO), is a leader in clinical development and patient access, providing solutions to pharmaceutical, biotechnology, and medical device clients across more than 20 therapeutic areas. With over 19,000 employees operating in more than 90 countries, Fortrea is committed to transforming drug and device development.
Job Responsibilities
- Ensuring adherence to Standard Operating Procedures (SOPs).
- Managing and maintaining contract tracking, status systems, and both paper and electronic file systems.
- Assisting in processing and maintaining agreements in coordination with clinical study teams and contract status reporting.
- Supporting Contracts Specialists with populating, mailing, scanning, and tracking contracts.
- Participating in team discussions to improve departmental processes.
- Monitoring studies for compliance with internal processes or Sponsor requirements.
- Reviewing amendments such as clinical study documents, Protocols, and ICF amendments; negotiating contracts with sites and sponsors.
- Performing other department-related duties as assigned.
How to Apply
Apply through the following link: Fortrea Careers
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