ClinChoice is seeking a Freelance Clinical Research Associate to join their team. The successful candidate will work on diverse projects for pharmaceutical, biotechnology, medical device, and consumer health companies. This role involves executing clinical trials to enhance patient lives.
- Assisting in site selection and evaluation
- Training site staff on study procedures
- Conducting and reporting periodic monitoring visits
- Managing investigational products and trial materials
- Cooperating with site staff on safety issue reporting
- Conducting study termination activities
- Serving as the main contact person for sites
- Providing quality control support for clinical data
- Developing training materials
- Assisting in contract negotiation with sites
- Assisting in study preparation, including CRF design
- Supporting the submission process
Requirements:
- University Degree in scientific medical or paramedical disciplines
- Previous proven experience as a CRA, performing on-site monitoring activities
- Strong knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirements
- Fluent in English and French
- Proficiency in Microsoft Office (e.g. Word, Excel, Outlook)
- Willingness to travel
ClinChoice offers:
- Professional development opportunities
- Excellent work-life balance
- Collaborative, quality-focused "one-team" culture
Apply
ClinChoice
ClinChoice is a global, full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 28 years of experience, ClinChoice focuses on delivering high-quality results through its team of over 4,000 professionals across the Americas, Europe, and Asia-Pacific. The company emphasizes employee development and maintains a supportive culture, driven by a mission to accelerate the development of innovative drugs and devices for a healthier world.