Senior Clinical Research Coordinator (SoCRA Certified)

Health Partners Plans

Philadelphia (Philadelphia County)

On-site

USD 70,000 - 100,000

Full time

4 days ago
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Job summary

Thomas Jefferson University seeks an experienced clinical research professional to oversee day-to-day activities of a clinical trial in line with GCP. Responsibilities include protocol coordination, data management, regulatory submissions, and staff training.

The role requires SOCRA certification or equivalent experience, and strong experience with IRB processes, workflow design, and QA of trial data. US-based on-site work at Jefferson facilities.

Qualifications

  • Minimum Qualifications: High School Diploma or GED with 5 years clinical research experience, or 2 years with Bachelor's and 2 years experience, or 1 year with Master's and 1 year experience.
  • SoCRA Certification is an additional qualification.
  • Regulatory submission experience (IRB) and GCP knowledge are required by protocol.
  • Ability to train and orient new staff and develop workflows.

Responsibilities

  • Oversee day-to-day activities of a clinical trial per GCP.
  • Train and supervise research staff on trial procedures.
  • Prepare and submit materials for IRB and regulatory bodies.
  • Track expenses and manage documentation for payments.
  • Perform quality control of trial data and manage patient data.
  • Design electronic capture databases and manage data collected.

Education

High School Diploma/GED with 5 years clinical research experience
Bachelor's degree with 2 years clinical research experience
Master's Degree with 1 year clinical research experience
SoCRA Certification

Job description

Thomas Jefferson University seeks an experienced clinical research professional to oversee day-to-day activities of a clinical trial in line with GCP. Responsibilities include protocol coordination, data management, regulatory submissions, and staff training.

The role requires SOCRA certification or equivalent experience, and strong experience with IRB processes, workflow design, and QA of trial data. US-based on-site work at Jefferson facilities.

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