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Role Overview:
- Perform comprehensive on-site or remote monitoring activities for clinical trials.
- Ensure investigator qualifications and site resources meet study requirements.
- Train site staff and assist with regulatory submissions.
Qualifications:
- College or university degree in Life Sciences or equivalent experience.
- Extensive on-site monitoring experience in phase 2/3 trials, ideally in oncology or rare disease.
- Full working proficiency in English and French.
Work Environment:
- Join a passionate, collaborative team of clinical research experts.
- Value-driven culture emphasizing quality, integrity, agility, and belonging.
- Opportunities for career growth and work-life balance.
Ergomed
Ergomed is a specialist clinical research organization focused on rare disease and oncology trials. With a collaborative international team across North America, South America, Europe, Asia, and Australia, the company values teamwork, flexibility, and work-life balance.