Clinical Research Associate II

Summary

Join Ergomed Group, a rapidly expanding CRO specializing in Oncology and Rare Disease, as a Clinical Monitor. You will perform on-site or remote monitoring visits throughout the study lifecycle, ensuring investigational sites meet study requirements. Responsibilities include training site staff, verifying investigator qualifications, and supporting regulatory submissions. The ideal candidate possesses extensive phase 2/3 monitoring experience, a life sciences degree or equivalent, and fluency in English and French. Ergomed offers a supportive work environment, career development opportunities, and a global team.

Requirements

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials
• Full working proficiency in English and French
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel

Responsibilities

• Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study
• Identify the investigators and verify that the investigator has adequate qualifications, resources, facilities, equipment and staff to conducting the clinical study throughout the study period
• Train investigational site staff as necessary
• When applicable, support preparation of regulatory and / or EC submissions

Benefits

• Training and career development opportunities internally
• Strong emphasis on personal and professional growth
• Friendly, supportive working environment
• Opportunity to work with colleagues based all over the world, with English as the company language