Clinical Research Coordinator – Early Pregnancy Biobank

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

Benefits offered by this job

Healthcare benefits

Tuition benefits

Retirement plans

Job summary

University of Pennsylvania, Perelman School of Medicine, seeks a Clinical Research Coordinator A to organize and implement a research study in obstetrics and gynecology. You will recruit subjects, manage data entry, collect biospecimens, and ensure regulatory compliance under IRB and FDA guidelines.

The role emphasizes biobank development and abstracting pregnancy outcome records, with a strong focus on ethics, accuracy, and workflow efficiency in a busy clinical research setting.

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, includes; 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 includes: 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, included possessing an in-depth knowledge of the federal regulations and guidance documents for the conduct of clinical studies and human subject protection
• Other duties and responsibilities as assigned

Skills

Data management

IRB coordination

REDCap

EMR experience

Regulatory compliance

Education

Bachelor of Science

Tools

REDCap

Job description

University of Pennsylvania, Perelman School of Medicine, seeks a Clinical Research Coordinator A to organize and implement a research study in obstetrics and gynecology. You will recruit subjects, manage data entry, collect biospecimens, and ensure regulatory compliance under IRB and FDA guidelines.

The role emphasizes biobank development and abstracting pregnancy outcome records, with a strong focus on ethics, accuracy, and workflow efficiency in a busy clinical research setting.