Clinical Research Coordinator – Early Pregnancy Studies

University of Pennsylvania; Woodworth (OH); On-site; USD 43,000 - 52,000; Full time

Benefits offered by this job

Health benefits

Tuition benefits

Retirement plans

Flexible work hours

Wellness programs

Job summary

The University of Pennsylvania's Perelman School of Medicine seeks a Clinical Research Coordinator A to organize and implement a study in early pregnancy. Responsibilities include subject recruitment, data entry, biospecimen collection, and regulatory management, working with multiple investigators to build a biobank and abstract information from medical records.

This role emphasizes adherence to federal regulations, Good Clinical Practice, and collaboration; the ideal candidate has a BA/BS and

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 documentations.
• 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 regulatory requirements.

Skills

Data collection & abstraction

Team collaboration

Education

Bachelor of Science

Tools

REDCap

Job description

The University of Pennsylvania's Perelman School of Medicine seeks a Clinical Research Coordinator A to organize and implement a study in early pregnancy. Responsibilities include subject recruitment, data entry, biospecimen collection, and regulatory management, working with multiple investigators to build a biobank and abstract information from medical records.

This role emphasizes adherence to federal regulations, Good Clinical Practice, and collaboration; the ideal candidate has a BA/BS and