Clinical Project Associate I

Profile

Position Role/Tile: Clinical Project Associate I
Location:
Foster City, CA
Duration : 18 months
Responsibilities:
The position entails working under general supervision for routine tasks and with detailed instructions on new assignments.
Tracks and prepares study-specific information utilizing databases, spreadsheets, and other tools.
Files drug shipments, drug returns, and assists with in-house drug reconciliation.
Under close supervision, reviews and participates in the quality assurance of data or documents.
Reviews and confirms site payments monthly.
Arranges meeting logistics.
Drafts meeting agendas and assists in preparing or taking meeting minutes.
Interacts with other departments, as directed, to complete assigned tasks.
Excellent verbal, written communication, and interpersonal skills are required.
Must be familiar with Word, PowerPoint, and Excel.
Knowledge of FDA and or EMEA Regulations, ICH Guidelines, GCPs, and/or familiarity with standard clinical operating procedures is preferred.
Must be able to learn new processes quickly, stay organized while working on multiple studies, and be able to work both independently and as a team.
Job Requirements
Clinical Operations Setting, GCP, ICH, EMEA, FDA
Job Code:
50124434
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Recruiter
Nandini
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