Full-Time

Senior Clinical Research Coordinator

Updated on 8/1/2026

Jefferson Health

Jefferson Health

No salary listed

Philadelphia, PA, USA

In Person

Category
Biology & Biotech (1)

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Requirements
  • A high school diploma or equivalent with 6 years of clinical research experience, a bachelor's degree with 2 years of clinical research experience, or a master's degree with 1 year of clinical research experience.
  • Knowledge of Good Clinical Practice guidelines, clinical trial protocols, applicable regulations, and Institutional Review Board requirements.
Responsibilities
  • Work on observational and interventional research, including industry-sponsored and investigator-initiated clinical trials of novel treatments across multiple Neurology divisions.
  • Identify subjects, obtain informed consent, collect and enter data, process laboratory samples, and maintain study documentation according to federal regulations and Good Clinical Practice guidelines.
  • Oversee day-to-day clinical trial activities in accordance with Good Clinical Practice guidelines.
  • Independently manage or assist with clinical trials from startup through closeout.
  • Coordinate protocol-related activities, including patient screening, recruitment, enrollment, and informed consent.
  • Conduct feasibility assessments and study planning activities.
  • Manage clinical trial data and biological specimens.
  • Prepare for sponsor monitoring visits and audits.
  • Prepare and maintain regulatory and Institutional Review Board documentation.
  • Ensure study procedures are conducted in compliance with protocol requirements and applicable regulations.
  • Train and supervise research staff on Good Clinical Practice and study-specific procedures.
  • Assist with onboarding and training new team members.
  • Develop and revise workflows, training materials, standard operating procedures, and guidance documents.
  • Participate in departmental workgroups and process improvement initiatives.
  • Prepare and submit materials to the Institutional Review Board and other regulatory bodies in a timely manner.
  • Maintain subject enrollment and tracking logs.
  • Track study-related expenses and submit documentation for grant and study payments.
  • Perform quality control reviews to ensure data integrity and regulatory compliance.
  • Organize and maintain study records and patient documentation.
  • Design and manage electronic data capture databases, when applicable.
  • Provide clerical and technical support to ensure adherence to research protocols and data quality.

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