Job Description
**Summary**:
Responsible and accountable for execution of assigned clinical research tasks related to IITs, MAPs, RCs, and NIS/LIS
**About the Role**:
LI-Hybrid
Location: Mexico City
**Key Responsibilities**
- Accountable for the accuracy and timeliness of trial information in all trial databases and tracking systems.
- Facilitates MRC and SRC review of concepts
- Timely processing of MAP requests, maintenance of request and closure
- Interfaces with the disease area(s), global and US clinical team members, regulatory affairs, drug supply, data management, finance and other relevant functional areas
- Preparation of trial related documentation, TMF maintenance: project files including ethics committee approvals; curricula vitae of investigators and study personnel; clinical investigators brochure; protocols; case report forms instructions; consent documents; clinical trial material shipping orders; start-up meeting attendance documentation; le...