• Assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring) • Prepares meeting materials, protocol deviation management • May support a single study or multiple studies • May lead a study with limited scope (e.g., Survival Follow-up) • Liaises with cross-functional lines as appropriate • May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives