Clinical project Associate

Title: Clinical Project Associate

Duration: 06 Months

Location: Foster City, CA

Job Responsibilities & Skills

• Project involvement will be in an administrative role.
• Provides administrative support to the Clinical Operations function including set-up, maintenance and reconciliation of the Trial Master File (including RDMS) for studies on an as needed basis.
• The position entails work under general supervision for routine tasks and with detailed instructions on new assignments.
• Tracking and preparing study-specific information utilizing databases (GILDA, DataVision), spreadsheets, and other tools.
• Distributes updated study related documents (i.e. Investigative Brochures, package inserts) to study teams and internal departments as requested by the CTMA or CTM.
• Under close supervision reviews and participates in the quality assurance of data or documents including and not limited to GILDA and DataVision.
• Arranges meeting logistics.
• Drafts meeting agendas and assists in preparing meeting minutes.
• Interacts with other departments, as directed, to complete assigned tasks. 

Skills/Experience requirements:

• Excellent verbal and written communication skills and interpersonal skills are required.
• Must be able to work both independently and as part of a team. 
  
  

Education/Experience:

• Typically requires a BS or BA in a relevant scientific discipline.
• 2+ years of experience and an Associates degree.
• Must be familiar with Word, Outlook, PowerPoint, and Excel. Knowledge of FDA and or EMEA

Kind Regards,

Sabanaaz Shaikh

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

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