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Clinical Research Associate
IQVIA Argentina
Reading
On-site
GBP 80,000 - 100,000
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Job summary
An established industry player is looking for a Clinical Research Associate to join their mission of creating a healthier world. This role offers a fantastic opportunity for those who thrive in supportive environments and seek collaborative teamwork. You will be responsible for site management and monitoring, ensuring adherence to Good Clinical Practice and ICH guidelines while providing essential training to study sites. With a focus on career growth and technology-enabled resources, this position promises to be both impactful and fulfilling. If you're passionate about making a difference in clinical research, this is the perfect opportunity for you.
Benefits
Supportive leadership
Variety of career opportunities
Collaborative teams
Technology-enabled resources
Qualifications
- 12 months minimum experience in independent on-site monitoring.
- In-depth knowledge of GCP and ICH guidelines.
Responsibilities
- Manage and monitor clinical sites through various stages.
- Provide training and maintain monitoring visit reports.
Skills
Site management
Monitoring
Subject recruitment
Good Clinical Practice (GCP)
International Conference on Harmonization (ICH)
Education
Life science degree
Tools
Technology-enabled resources
Job description
IQVIA are seeking a Clinical Research Associate in the UK to join us on our mission to help create a healthier world.
Excellent opportunity for CRAs who would value:
- Supportive leadership and collaborative teams
- A variety of career opportunities to allow you to grow as we grow
- Technology-enabled resources that make doing your job more efficient
Responsibilities
- Site management and monitoring (site selection, site initiation, routine monitoring and close-out visits)
- Working with sites to adapt, drive and track subject recruitment plan
- Providing protocol and study training to assigned sites
- Creating and maintaining monitoring visit reports and action plans
Requirements
- Experience of independent on-site monitoring (12 months minimum)
- In-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Life science degree educated or equivalent industry experience
- Flexibility to travel to sites as required
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
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