The Clinical Project Specialist position at Lilly Centre for Clinical Pharmacology is a one-year contract role focused on managing and implementing clinical trials in compliance with relevant regulations and guidelines. The candidate will serve as a liaison between the clinical research unit and sponsors, ensuring effective communication and operational consistency throughout the study lifecycle
Job Summary
The role is responsible for the effective management and implementation of clinical trials in the Clinical Research Unit in compliance with SOPs and GCP guidelines.
The incumbent serves as the primary liaison between the CRU study team, sponsors, monitors, and Ethics/Institutional Review Board on operational matters.
Key responsibilities include managing study timelines, overseeing safety reporting, coordinating site visits, and ensuring the maintenance of investigator trial master files.
Matching Summary
Match Score: 85
The Clinical Project Specialist position at Lilly Centre for Clinical Pharmacology is a one-year contract role focused on managing and implementing clinical trials in compliance with relevant regulations and guidelines. The candidate will serve as a liaison between the clinical research unit and sponsors, ensuring effective communication and operational consistency throughout the study lifecycle.
Skills & Requirements
Must-have
5 years clinical research experience
GCP knowledge and compliance
CRU operations management
Protocol development and review
IRB submission coordination
Nice-to-have
Strong leadership skills
Excellent communication abilities
Proactive problem solving
Microsoft Office proficiency
Vendor management experience
Key Requirements
Diploma or Degree in Nursing, Science or health-related field