Clinical Trials Site Manager

Company: SQRL
Location: Annapolis
Posted on: June 25, 2022

Job Description:

Are you ready to join an exploding CRO with a focus on neurology, family practice, and dermatology, with plans to include additional therapy areas in the near future? They are looking to add a new Site Manager to their two sites located in Rockville and Annapolis, Maryland. DAY IN THE LIFE:On a day to day the Site Manager will be responsible for building and managing a team of Clinical Research Coordinators, site assessments, pre-trial assessments, site initiation, subject recruitment and retention, monitoring and close-out, conducting pre-study site selection visits and assessments, Ensuring site study supplies are adequate for trial conduct, work to ensure enrollment goals of the study center are being met, Monitors patient visits, and ensure the successful buildout of the new research site.RESPONSIBILITIES

• Oversee the conduct of your assigned site; responsible for the training of staff/providers, process development, point of contact for the Directors of Operations and cross-functional teams.
• Work closely with Business Development and Feasibility on study placements.
• Accountable for enrollment success at sites across all studies; understand revenue expectations.
• Develop and implement patient recruitment strategies; actively recruit to achieve enrollment targets.
• Maintain a significant depth of knowledge and experience in coordinating across multiple therapeutic areas.
• Coordinate as primary CRC on at least six studies of medium to high complexity and back-up CRC on other studies when needed.
• Assist in the development of the annual site roadmap.
• Perform quality control checks on source documentation and regulatory.
• Work closely with the Quality Assurance Department to ensure quality at the site; create processes and CAPAs to improve trends.
• Support the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, laboratory handling manuals, etc.).
• Adhere to an IRB approved protocol
• Coordinate protocol related research procedures, study visits, and follow-up
• Facilitate site qualification, study initiation, and monitoring visits, and study close-out activities MUST-HAVES:
  • 4 - 8 year of experience as a Clinical Research Coordinator (sponsor-backed trials)
  • 1+ year of Management experience
  • Bachelors degree preferred but not required

Keywords: SQRL, Baltimore , Clinical Trials Site Manager, Professions , Annapolis, Maryland