As a Clinical Operations Specialist, you will lead and coordinate activities related to submissions according to ICH GCP, international and local regulations, and relevant GSK standards
Job Summary
As a Clinical Operations Specialist, you will lead and coordinate activities related to submissions according to ICH GCP, international and local regulations, and relevant GSK standards.
You will be responsible for coordinating and managing contracts and legal documents for clinical studies, including communication of updates and documentation of activities according to GSK SOPs and local legislation.
GSK aims to positively impact the health of 2.5 billion people by the end of the decade through innovative vaccines and medicines, uniting science, technology, and talent.
Matching Summary
As a Clinical Operations Specialist, you will lead and coordinate activities related to submissions according to ICH GCP, international and local regulations, and relevant GSK standards.
Skills & Requirements
Must-have
Contract negotiation and execution
Clinical trial documentation management
ICH GCP compliance
Local and international regulations
Budget negotiation with sites
Third-party vendor management
Nice-to-have
Proactive risk identification
Cross-functional team collaboration
Training and coaching skills
Key Requirements
Bachelor's degree or equivalent in a scientific field