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Senior Clinical Research Associate
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Regulatory Compliance
Communication
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Department:
- Clinical Monitoring
Job Description:
- Perform on-site or remote monitoring visits to ensure facilities and staff are adequate for study conduct.
- Identify investigators and verify qualifications, resources, and equipment.
- Train investigational site staff and support regulatory submissions.
Qualifications:
- College/University degree in Life Sciences or equivalent.
- Extensive on-site monitoring experience in phase 2/3 trials, ideally oncology or rare disease.
- Full working proficiency in English and French.
Additional Information:
- Travel required nationally and to France and Belgium.
- Collaborative team environment with focus on work-life balance.
Ergomed
Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. They have a collaborative, international team with colleagues across the globe, valuing teamwork, flexibility, and work-life balance.