Remote
Clinical Research Associate
About this role
π Description Serve as the primary point of contact for assigned investigative sites, providing relevant study Build effective working relationships with investigators and site staff, and support their Conduct site evaluation, initiation, routine monitoring, and close-out activities in accordance Support the safety and protection of study participants throughout the clinical trial. Develop and adapt site engagement strategies based on study requirements and local site insights Apply knowledge of the protocol, scientific principles, therapeutic area, and patient journey to π― Requirements Degree or equivalent qualification in a health-related discipline, such as Medicine, Life Sciences At least one year of clinically related experience, including a minimum of six months of experience Familiarity with risk-based monitoring approaches, including on-site and remote monitoring.
Knowledge of relevant therapeutic areas and the ability to apply scientific concepts to clinical Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies. Fluency in French, Dutch, and English is required.
Source listing: empllo_remote