A Clinical Trial Lead (CTL) is a member of the project team responsible for the execution of the clinical trial(s) at the site level, accountable for development and execution of the clinical monitoring plan (CMP), site identification and selection, CRA and site training, development of CRA and site materials, trackers, and logs necessary to track and document deliverables. The lead CRA will review monitoring visit reports and track actual to projected variables and parameters related to CRA & site activities. All activities will be in compliance with cGCPs, country specific regulations, ICH Guidelines, and SOPs.
Education: Bachelor’s degree, in biological sciences, healthcare, or pharmacy medicine preferred
Experience: 5+ years related experience. CRA level experience (both CRO and industry experience are acceptable). Prefer scientific discipline and multiple therapeutic experiences. The candidate must have:
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