Clinical Research Site Manager

The Manager, Site Operations is responsible for managing the clinical operations staff, training and onboarding of new staff, managing quality and compliance of clinical Work closely with and in support of the Site Director. Able to perform coordinator as well as supervisor duties and fill in during the absence of site coordinators. Able to function as lead coordinator on select protocols. Must be able to work independently and with all staff and customer levels.

Position Qualification Requirements:

Education: Bachelor’s degree preferred; Experience: 2+ years of clinical research management experience or equivalent applicable experience in clinical research industry

-Covid-19 vaccine required

Position Responsibilities:

• Work with the Site Director to meet/exceed the site’s financial, operational and study-specific targets.
• Support the identification of strategies to expand the research capabilities at the site – in line with the overall site business plan.
• Support the implementation and maintenance of VCR quality standards at the site ensuring that the conduct of clinical studies and the collection of patient data is in accordance with ICH GCPs.
• Work with the Site Director to address any study and/or clinical quality related matters.
• Ensure timely and appropriate communications occur with Sponsors and IRBs as necessary.
• Support the development of site staffing plans to ensure the successful and efficient conduct of research studies. Identify and fulfill any site resource needs which are necessary to successfully conduct and/or recruit research studies.
• Support or lead the development of the patient recruitment plan and patient outreach process for studies. Make ongoing adjustments/modifications to recruitment strategies based upon the timely review of results to ensure study-specific targets are being met.
• Manage the performance of site staff members, delegating appropriate and challenging assignments to encourage growth, development and responsibility. Responsible for supporting the ongoing training needs of site staff members are met.
• Communicate performance expectations and guidelines to site staff members.
• Identify and manage issues, concerns and problems related to staff conduct and performance.
• Identify and build relationships with outside medical practices, pharmacies, and other health care professionals/organizations to aid in the patient recruitment process.
• Support business development activities on behalf of the site and VCR with sponsors, CROs, CRAs and any third-party study vendors, as appropriate.
• Share best practices with other VCR site locations with the goal of raising the overall level of operational competencies at VCR.
• Support the completeness, accuracy and timeliness of Feasibility Questionnaires, CDAs, CVs and essential regulatory documents from study start-up phase until site initiation.
• Attend industry and VCR meetings relevant to the position of Manager, Site Operations.
• Manage facility and IT needs to ensure smooth and efficient operations.