Fortrea Development India Private Limited Interview Questions, Process, and Tips

I was responsible for regulatory submissions, ensuring compliance with regulations, and communicating with regulatory agencies.

• Prepared and submitted regulatory documents for product approvals

• Ensured compliance with regulatory requirements and guidelines

• Communicated with regulatory agencies to address any issues or inquiries

I am currently working as a Centralized Study Specialist and TMF Specialist.

• Responsible for managing and coordinating centralized study activities

• Ensure compliance with study protocols and regulatory requirements

• Maintain Trial Master File (TMF) and ensure its completeness and accuracy

• Collaborate with cross-functional teams to ensure smooth study operations

• Provide support in data collection, analysis, and reporting

• Condu...read more