Clinical Research Coordinator B

6 days ago


Philadelphia, Pennsylvania, United States University of Pennsylvania Full time
Job Summary

This is a challenging and rewarding role that requires a high level of organization, attention to detail, and excellent communication skills. As a Clinical Research Coordinator B, you will be responsible for facilitating the conduct of research protocols in the Department/Center, ensuring good clinical practice, and working collaboratively with research personnel.

Key Responsibilities
  • Protocol Management: Coordinate the conduct of research protocols, including maintenance of study documentation, data collection, and regulatory compliance.
  • Subject Recruitment and Enrollment: Recruit, screen, and enroll participants as specified per protocol, ensuring patient safety and data quality.
  • Data Management: Collect, enter, and process data, as well as manage study-related diagnostic testing and procedures.
  • Communication and Collaboration: Communicate effectively with research personnel, investigators, and external sites, and work collaboratively to ensure the success of research projects.
  • Regulatory Compliance: Ensure compliance with all federal, state, University, and GCP guidelines, and maintain relevant trainings and certifications.
Requirements
  • Education and Experience: Bachelor of Science and 2 to 3 years of experience in clinical research or a related field.
  • Skills and Qualifications: Excellent communication and organizational skills, attention to detail, and ability to work in a fast-paced environment.
What We Offer

The University of Pennsylvania offers a competitive benefits package, including excellent healthcare and tuition benefits, generous retirement benefits, and a wide variety of professional development opportunities.



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