Clinical Research Coordinator - Multi-Center Trials & IRB Support

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

Benefits offered by this job

Health insurance

Retirement plans

Tuition benefits

Flexible work hours

Job summary

University of Pennsylvania in Philadelphia, PA seeks a Clinical Research Coordinator A to manage multiple clinical trials and assist with IRB filings, manuscript preparation, and grant proposals. You will coordinate screening, enrollment, data collection, and regulatory documentation under the supervision of the Principal Investigator.

The role requires a Bachelor of Science and 1–2 years of related experience, with funding contingent terms.

Qualifications

• Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.
• This position is contingent upon funding.

Responsibilities

• Conduct clinical investigation utilizing GCP and regulatory requirements.
• Coordinate and conduct human subject clinical study including recruitment, scheduling, informed consent, and data management.
• Maintain regulatory binders and IRB submissions/renewals.
• Document and report study procedures and adverse events in a timely manner.
• Attend team meetings and communicate accurately with Investigators and study staff.

Skills

GCP knowledge

Data management

Subject recruitment

Education

Bachelor of Science

Job description

University of Pennsylvania in Philadelphia, PA seeks a Clinical Research Coordinator A to manage multiple clinical trials and assist with IRB filings, manuscript preparation, and grant proposals. You will coordinate screening, enrollment, data collection, and regulatory documentation under the supervision of the Principal Investigator.

The role requires a Bachelor of Science and 1–2 years of related experience, with funding contingent terms.