Director Clinical Research

Found in: Appcast Linkedin GBL C2 - 2 weeks ago

New York, United States The Goodkind Group, LLC Full time

Healthcare Facility located in (Queens, NY) is seeking a skilled Clinical Research Administrator to fill the Assistant Director of Research position | This position requires some local travel to other medical facilities within Queens, NY.


Education and Work Experience:

• Master's degree or equivalent Required

• PhD, MD, or equivalent preferred

• At least 5 years' experience working in clinical research.

• Managerial experience required within hospital settings.


Duties and Responsibilities:

  • Assist in securing funded clinical research contracts that are feasible and aligned with health system goals.
  • Ensure that applicable regulatory requirements are being met during execution of research trials.
  • Assist in working with Finance and Legal to contract and budget research trials.
  • Oversee CRAs, research pharmacist, research nurse, and other staff within the department.
  • Work with investigators in clinical departments to execute contracts effectively.
  • Work with research coordinators in clinical departments involved in trials to achieve study goals.
  • Work with the research compliance personnel and the IRB for regulatory requirements.
  • Identify interpersonal and individual challenges hindering achievement of departmental goals.
  • Discuss departmental issues with the director to determine corrective action measures or areas for improvement.
  • Work with IT support and EPIC staff to integrate clinical trial workflows into the electronic medical record. Manage charges related to clinical research in the electronic medical record.
  • Prepare written SOPs and develop quality assurance plans.
  • Prepare for regulatory audits.
  • Perform other duties as requested by the Director or the Department or Research Operating Officer


Additional Responsibilities:

  • Regular undergo continuing education activities to enhance job performance.
  • Attend relevant conferences and meetings that are instrumental in achieving any health network goals.
  • Local and national travel may be requested.
  • Performs other incidental and related duties as required and assigned.

Skills and Knowledge:

  • Strong written and oral communication skills with background in medicine or biomedical science
  • Experience managing clinical trial finances.
  • Proficient in the use of Microsoft Word, PowerPoint, and Excel. Ability to learn new software as part of the position, including data entry systems (Rave, Inform, etc.)
  • Expertise in GCP and clinical trial oversight. SOCRA certified or eligible preferred.
  • Experience with electronic health records. Reports to the Director of the Department of Clinical Research

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