Clinical Project Associate

Job description

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 procedure s 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 kep t confidential according to EEO guidelines. With Regards, Abhishek Singh 650-399-0881 Clinical Recruiter Integrated Resources, Inc. Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.