Senior Study Manager Description of Services Assists the SM Study Lead and study team with the operational conduct of clinical studies (e.g., CTT minutes, clinical supplies planning/tracking, lab specimen tracking, imaging data reconciliation, status update reports, study closeout activities) May support a single study or multiple studies Lead a study with limited scope (e.g., Survival Follow-up) Responsible for tracking study timelines and will be proficient in project management tools Interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical study objectives Minimum Years of Experience At least 7 years Pharmaceutical and/or clinical drug development experience (such as pharmaceutical/biopharma companies, CRO) in the last 5 years required 2 years experience leading global studiesTA-specific experience beneficial (Oncology preferred) Demonstrated oral and written communication skills Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required; OneNote experience preferred. Educational RequirementsBS/BA/MS/PhD
