Associate Director, Clinician

Responsibilities:Review and oversight of the adequacy of other clinical assessments (as appropriate).Clinical development plan, clinical protocol development, study planning and initiation.Provide medical input during development and updates to the clinical development plan. Provide medical input during clinical protocol development and Informed Consent Document (ICD).Medical review of country feedback during protocol feasibility to ensure understanding and mitigation of any feedback which may impact future protocol compliance, risks to subject safety or data integrity (e.g. understanding of local standard of care and impact on ability to execute clinical protocol). This is performed in collaboration with the Regional Clinical Site Leads (RCSLs) if they are assigned to the clinical trial.Provide study team with medical advice for all medical issues during risk assessment and mitigation planning to enable quality, compliance and patient safety at the trial, site and patient level.Provid...