The Senior Clinical Research Associate will play a crucial role in the planning, execution, and management of clinical trials
Job Summary
The Senior Clinical Research Associate will play a crucial role in the planning, execution, and management of clinical trials.
Responsibilities include performing site selection, initiation, monitoring, and close-out visits while ensuring data integrity and regulatory compliance.
IQVIA is a leading global provider of clinical research services dedicated to accelerating the development of innovative medical treatments.
Matching Summary
The Senior Clinical Research Associate will play a crucial role in the planning, execution, and management of clinical trials.
Skills & Requirements
Must-have
4 years on-site monitoring experience
In-depth knowledge of GCP and ICH guidelines
Proficiency in CTMS and EDC systems
Bachelor's degree in health care or science
Ability to travel as required
Nice-to-have
Strong organizational and time management skills
Excellent communication and interpersonal skills
Ability to work independently and collaboratively
Good basic knowledge of regulatory requirements
Advanced English proficiency
Key Requirements
Bachelor's degree in health care or scientific discipline