Ob/Gyn Clinical Research Coordinator

Clay Today; Philadelphia (Philadelphia County); On-site; USD 43,000 - 52,000; Full time

Benefits offered by this job

Tuition benefits

Wellness programs

Flexible work hours

Retirement plans

Job summary

The Clinical Research Coordinator A at University of Pennsylvania in Philadelphia will organize and implement a research study in obstetrics and gynecology, coordinating patient recruitment, data entry, and biospecimen collection.

Responsibilities include managing IRB submissions, ensuring protocol compliance, and coordinating data management and regulatory activities with investigators. A BS with 1–2 years of experience is required; experience with EMR/REDCap is a plus.

Qualifications

• Bachelor of Science and 1–2 years of experience required.
• Experience with electronic medical records (EMR) and REDCap is a plus.

Responsibilities

• Coordinate and conduct clinical studies, including subject recruitment and informed consent.
• Manage chart maintenance, data entry, and regulatory documentation.
• Oversee IRB submissions and renewals per FDA and IRB guidelines.
• Ensure protocol compliance and maintain source data and documents.
• Oversee blood sample processing, biobank activities, and data analysis.
• Order supplies, manage equipment, and educate patients and families.

Skills

Data collection

Subject recruitment

Informed consent

Regulatory compliance

IRB coordination

Education

Bachelor of Science and 1-2 years experience

Tools

REDCap

EMR

Job description

The Clinical Research Coordinator A at University of Pennsylvania in Philadelphia will organize and implement a research study in obstetrics and gynecology, coordinating patient recruitment, data entry, and biospecimen collection.

Responsibilities include managing IRB submissions, ensuring protocol compliance, and coordinating data management and regulatory activities with investigators. A BS with 1–2 years of experience is required; experience with EMR/REDCap is a plus.