Clinical Research Coordinator — OB/GYN (Flexible Hours)

University of Pennsylvania

United (PA)

On-site

USD 43,000 - 52,000

Full time

3 days ago
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Job summary

The University of Pennsylvania, Perelman School of Medicine, in Philadelphia, seeks a Clinical Research Coordinator A to organize and implement a pregnancy-related study. You will manage subject recruitment, data entry, visits and follow-up, biospecimen handling, and regulatory tasks in collaboration with several investigators.

The position emphasizes adherence to good clinical practice, IRB submissions, and data quality, with a focus on early pregnancy research and biospecimen biobanking.

Qualifications

  • Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.
  • Experience with electronic medical records and REDCap is a plus.

Responsibilities

  • Coordinate and conduct clinical studies, including subject recruitment, informed consent, chart maintenance and data entry.
  • Coordinate IRB submissions and renewals in accordance with FDA and IRB guidelines.
  • Assure compliance with the protocol and regulatory requirements, including collecting, recording and maintaining data and source documents.
  • Oversee study preparation and blood sample processing and analysis.
  • Database management and analysis.
  • Ordering and stocking supplies, maintaining equipment.
  • Educate patients and family members.
  • Promote good clinical practice in the conduct of clinical investigations and federal regulations.

Skills

Data collection
EMR experience
REDCap

Education

Bachelor of Science and 1-2 years experience

Tools

REDCap

Job description

The University of Pennsylvania, Perelman School of Medicine, in Philadelphia, seeks a Clinical Research Coordinator A to organize and implement a pregnancy-related study. You will manage subject recruitment, data entry, visits and follow-up, biospecimen handling, and regulatory tasks in collaboration with several investigators.

The position emphasizes adherence to good clinical practice, IRB submissions, and data quality, with a focus on early pregnancy research and biospecimen biobanking.

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