Clinical Research Coordinator — Infectious Disease Trials

University of Pennsylvania; Philadelphia (Philadelphia County); On-site; USD 53,000 - 63,000; Full time

Benefits offered by this job

Health insurance

Tuition benefits

Retirement plans

Flexible work options

Job summary

University of Pennsylvania seeks a Clinical Research Coordinator B/C to coordinate HIV and infectious disease studies. The role requires on-site presence, interaction with participants, and compliance with GCP, IRB, and regulatory guidelines.

You will support investigators through protocol development, patient recruitment, data collection, and regulatory documentation, working across multiple trials including gene therapy projects. Penn offers strong benefits and development opportunities.

Qualifications

• Effective problem-solving abilities.
• Effective communication and writing skills.
• Strong organizational and time management skills.
• Flexible and able to multi-task.
• Strong attention to detail.
• Demonstrated ability to work as part of a team, as well as independently.
• Knowledge of IRB and human research protection regulations.
• Highly reliable and good work ethic.

Responsibilities

• Screen, recruit, and enroll consenting patients using Good Clinical Practice guidelines.
• Coordinate clinical trials and support investigators in trials for HIV and other infectious diseases.
• Assist in development of study documents and communication with regulatory boards.
• Schedule visits and testing, monitor protocol adherence, and ensure data quality.
• Prepare and maintain regulatory files, source documents, and CRFs.
• Participate in audits, monitoring visits, and data queries, coordinating with CROs and the FDA.

Skills

Communication

Problem-solving

Organization

Time management

Detail-oriented

Teamwork

Independence

IRB knowledge

Phlebotomy

Education

Bachelor's degree

Job description

University of Pennsylvania seeks a Clinical Research Coordinator B/C to coordinate HIV and infectious disease studies. The role requires on-site presence, interaction with participants, and compliance with GCP, IRB, and regulatory guidelines.

You will support investigators through protocol development, patient recruitment, data collection, and regulatory documentation, working across multiple trials including gene therapy projects. Penn offers strong benefits and development opportunities.