Support Study Manager

Study Manager Description of ServicesAssists 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 studiesMay lead a study with limited scope (e.g., Survival Follow-up)May be responsible for tracking study timelines and will be proficient in project management toolsMay interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical study objectivesMinimum Years of ExperienceAt least 2 year Pharmaceutical and/or clinical drug development experience (such as pharmaceutical/biopharma companies, hospital settings, research sites, clinical trial units, CRO, SMO) in the last 5 years requiredTA-specific experience beneficialDemonstrated oral and written communication skillsProficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required; OneNote experience preferred.Educational RequirementsBS/BA/MS/PhD