What are the responsibilities and job description for the Clinical Research Associate position at GForce Life Sciences?
Clinical Research Associate Lake Forest, IL
Must be able to work on a W2
12 month contract
Travel may be required
Primary Job Function
The Clinical Research Associates manages sites through life of trial and close-out, including, the implementation, coordination and conduct of clinical research activities in compliance with applicable Corporate and Divisional Policies and Procedures. Participate in site selection, provide feedback in the protocol development and database development; investigator meetings.
Core Job Responsibilities
- Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
- Ensures compliance with protocol and all regulatory policies, procedures and / or guidelines during clinical studies by training / guidance of investigators / study coordinators and site staff.
- Communication with site staff including coordinators, clinical investigators, and their site staff;
- Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
- Source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
- Verification that the investigator is enrolling only eligible subjects / samples;
- Ensures timely collection and review of study and regulatory documentation by obtaining, maintaining and controlling all necessary records and documentation according to procedures and regulations.
- Responsible for investigational product accountability and inventory;
- Verification and review of adverse events to confirm accurate data reporting in accordance with the protocol.
- Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;
- Timely completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
- Builds and maintains relationships with sites.
- Intermediate knowledge in regulations for applicable geographies and types of studies (IDE, non-significant risk, feasibility, exempt, etc.).
- Ensures validity of study by identifying / resolving discrepancies and obtaining missing data.
- Basic knowledge of Abbott Platforms, assays, and assay data.
- Basic knowledge of statistics
- Contributes to developing and writing clinical protocols, informed consent forms, case report forms, and other study aids for investigational products by addressing issues by interacting with appropriate personnel.
- Performs Quality Assurance Verification.
- Responsible for training peers
- Serves as a trainer for contract research organizations (CROs) needed for additional monitoring support.
- Participates on at least 2 projects
Minimum Education
Minimum Experience / Training Required
