Innovaderm Research Benefits Overview

Manage end-to-end clinical trial site start-up across European countries, including site selection, regulatory submissions, contracting, budgeting, activation, timelines, risk mitigation, and performance reporting. Lead cross-functional collaboration, coordinate with project managers and sponsors, and serve as the primary contact for start-up activities. The role requires clinical trial start-up expertise, leadership, project management, and the ability to operate in a matrixed, multi-country environment.

Coordinates clinical research site selection activities, including investigator identification, feasibility assessments, questionnaire distribution, qualification visits, site recommendations, and CTMS tracking. Builds relationships with research sites, supports project teams, reviews site performance issues, and contributes to departmental initiatives. Requires clinical research experience in biotechnology, pharmaceutical, or CRO settings, with knowledge of site selection, study start-up, contracts, and applicable clinical research regulations.

Coordinates clinical research site selection and feasibility activities, including identifying investigators, evaluating questionnaires, recommending sites, coordinating qualification visits, and tracking activities in a CTMS. Builds relationships with clinical research sites, supports site quality assessments, collaborates with sponsors and project teams, and contributes to departmental initiatives. Requires at least three years of clinical research experience, knowledge of good clinical practices and Health Canada and FDA guidelines, and strong English communication skills; French and dermatology experience are assets.