Clinical Project Associate

• The position works under general supervision for routine tasks and with detailed instructions on new assignments
• Knowledge of FDA and EMA Regulations, ICH Guidelines, GCP, and familiarity with standard clinical operating procedures
• Must be familiar with Word, PowerPoint, and Excel
• Excellent verbal and written communication skills
• Must be able to work both independently and as part of a team
• Tracks and prepares study-specific information utilizing databases, spreadsheets, and other tools
• Reviews and participates in the quality assurance of data or documents
• Arranges meeting logistics, agendas, and assists with minutes
• Interacts with other departments, as directed, to complete assigned tasks
• Serves as back up providing verbal and written communication with study personnel
• Assists with development of documents and standard forms
• Travel may be required

• Typically requires a BS or BA in a relevant scientific discipline.
• Registered Nurse with relevant experience (2 or 3 year certificate).

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus.

Thank you.

Kind Regards,

Harris Kaushik

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - (650)-399-0891

Gold Seal JCAHO Certified ™ for Health Care Staffing

“INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)