Clinical Project Associate

• 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, spreadsheets, and other tools. Processes drug shipments, drug returns, and assists with in-house drug reconciliation.
• Orders and maintains inventory of clinical supplies. Orders and ships case report forms. Assists with development of documents for site binders.
• Assembles and prepares distribution of site binders. Serves as CRA back up providing verbal and written communication with study personnel.
• Under close supervision reviews and participates in the quality assurance of data or documents. Arranges meeting logistics.
• Drafts meeting agendas and assists in preparing meeting minutes. (Interacts with other departments, as directed, to complete assigned tasks.
• May assist with monitoring visits under the direct supervision of senior staff. Travel may be required. Excellent verbal and written communication skills 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 a plus. Must be able to work both independently and as part of a team.

• Bachelors degree required with 2 years relevant work exp

All your information will be kept confidential according to EEO guidelines.

With Regards,

Abhishek Singh

650-399-0881

Clinical Recruiter

Integrated Resources, Inc.