Description
IQVIA Belgium is seeking a motivated Senior Clinical Research Associate to join their unique and dynamic Sponsor dedicated model.
This role involves performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, administering protocol and related study training, evaluating study site practices, managing study progress, ensuring site documents are available, and creating documentation regarding site management.
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 the quality and integrity of study site practices
- Manage the progress of assigned studies
- Ensure copies/originals site documents are available for filing in the Trial Master File
- Create and maintain documentation regarding site management
- Collaborate and liaise with study team members for project execution support
Profile:
- University degree in scientific discipline or health care
- Minimum of 3 years of independent, on-site monitoring experience as a CRA
- Excellent communication skills in Dutch, French, and English
- Good knowledge of applicable clinical research regulatory requirements
- Exceptional interpersonal and cross-cultural communication skills
- Collaborative mindset to work effectively with cross-functional global teams
Benefits:
- Grow your career with access to development resources, training, and advancement opportunities
- Enjoy flexibility and trust to balance professional and personal commitments
- Expand therapeutic knowledge through dedicated learning and development programs
- Be part of a successful global organization with an excellent reputation and supportive culture
- Benefit from a company car, mobile phone, and attractive rewards and benefits package