Full-Time

Senior Clinical Research Coordinator

Posted on 8/22/2025

Jefferson Health

Jefferson Health

No salary listed

Philadelphia, PA, USA

In Person

Category
Biology & Biotech (2)
,
Required Skills
Google Cloud Platform
Requirements
  • High School Diploma or equivalent and 6 years of clinical research experience
  • Bachelor's degree and 2 years of clinical research experience
  • Master's Degree and 1 year clinical research experience
Responsibilities
  • Oversee the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP)
  • Run portions of clinical trials from startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting)
  • Conduct feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and/or IRB document preparation
  • Ensure all study procedures are conducted according to the protocol and applicable regulations
  • Assist with the orientation and training of new staff
  • Assist in the development of workflows, training documents, SOP/guidance document revision
  • Participate in work groups
  • Train and supervise research staff on the proper procedures for conducting a clinical trial per GCP
  • Prepare and submit all materials for the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol to ensure compliance in a timely fashion
  • Maintain accurate subject log, track expenses, submit appropriate documentation to Grant Administrator on a monthly basis for payment due for visits on all studies
  • Perform regular quality control assessments to ensure that clinical trial data is collected and stored per GCP
  • Organize and maintain documentation of all patient data
  • Design electronic capture databases, if appropriate, and manage all the data collected
  • Provide clerical and technical support to ensure adherence to research protocols and quality of information received

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