What are the responsibilities and job description for the CLINICAL RESEARCH ASSOCIATE position at McInnis, Inc.?
The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s), the Clinical Research Associate (CRA) will assist with study and site start-up activities by working directly with assigned clinical sites and assist with overall study execution. The CRA may also assist with data management, vendor management and site monitoring as needed.
Duties and Responsibilities
- Act as the primary point of contact with assigned clinical study sites during start-up activities;
- Working with finance and legal experts, drive contract and budget negotiations (or amendments) with assigned sites;
- Review site-level documents needed for IRB / EC / REC approval;
- Support study initiation, monitoring, audit and close-out phases of assigned clinical trials as prescribed in the sponsor SOPs and study monitoring plan;
- Ensure clinical study site documentation compliance according to GCPs, ICH and FDA regulations;
- Provide relevant, timely study subject updates to the Clinical Study Manager(s) (e.g., upcoming treatment dates, subject withdrawals, etc.);
- Facilitate timely and accurate communication flow between the clinical study sites, sponsor and applicable vendors;
- Collaborate with clinical study site and sponsor to troubleshoot and provide appropriate solutions to study-related issues, as appropriate;
- Assist in patient recruitment activities;
- Assist with the development of study-related documents as requested;
- Prepare accurate and timely study reports as requested;
- Work independently and under general supervision.
Education
Qualifications
