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Clinical Site Manager

3 months ago

Orlando, United States SQRL Full time

Highlights:


  • $90k - $117K + Bonus
  • Full Benefits and Consistent M-F schedule
  • Fast growing company with tons of opportunity


**This is an on-site position in the Clermont area of Orlando, FL. Please do not apply if you are seeking Hybrid or remote**


The Company:


Our client is a growing multi-site, multi-phase clinical research company with a network of locations in Boston and Northern MA, Portsmouth, NH, Charleston, SC, and Detroit, MI. They have established a strong presence across Phase I-IV studies and a variety of therapeutic areas.


The Role:


Responsible for coordinating and overseeing various aspects of clinical research studies, ensuring compliance with protocols and regulatory requirements.


  • Manage all day-to-day operations of the clinic and train and develop staff.
  • Organize all aspects of the clinical trials assigned and ensure success
  • Participate in investigator meetings, site initiation meetings
  • Work with our internal patient recruitment department for participant screening and enrollment and ensure compliance with protocol and all applicable regulations.
  • Conduct Informed consent process and conduct study related visits.
  • Monitor subjects per protocol requirements.
  • Assess, monitor, and report adverse events per protocol.
  • Maintain required records of study activity including source documentation, case report forms, drug dispensation records, and data management system entry.
  • Complete case report forms and resolve queries.
  • Provide assistance to fellow study coordinators including obtain, process and ship study related specimens
  • Manage quality assurance assigned protocols persite SOP’s.


Requirements:


  • 5+ years of Clinical Research experience as a Clinical Research Coordinator
  • Phlebotomy experience