Description
IQVIA Netherlands is seeking a motivated Senior Clinical Research Associate to join their unique and dynamic Sponsor dedicated model.
As a Senior Clinical Research Associate, you will perform site monitoring visits, work with sites to adapt and drive subject recruitment plans, administer protocol and related study training, evaluate study site practices, manage study progress, and ensure compliance with regulatory requirements.
Responsibilities:
- Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
- Work with sites to adapt, drive, and track subject recruitment plans
- Administer protocol and related study training to assigned sites
- Evaluate study site practices and escalate quality issues as needed
- Manage study progress, track regulatory submissions and approvals, and ensure compliance with regulatory requirements
Profile:
- Bachelor's degree in a scientific discipline or healthcare
- Minimum of 3 years of independent, on-site monitoring experience as a CRA
- Full professional fluency in Dutch and English
- Good knowledge of applicable clinical research regulatory requirements
- Organizational and problem-solving skills
- Exceptional interpersonal and cross-cultural communication skills
What we offer:
- Choice of company car or flexible mobility allowance
- Premium technology bundle
- Strong focus on career advancement
- Home office setup support and annual wellness reimbursement
- Comprehensive time-off policy and premium benefits package