Clinical Research Coordinator B

University of Pennsylvania

Philadelphia, Pennsylvania, US
$52,500.00 - $58,059.00 annual rate py
On-site
Manage phases of complex clinical trials
Ensure compliance with good clinical practice
Coordinate with partnering institutions
The Clinical Research Coordinator B will manage phases of complex clinical trials under general supervision, ensuring compliance with good clinical practice and coordinating with partnering institutions

Job Summary

  • The Clinical Research Coordinator B will manage phases of complex clinical trials under general supervision, ensuring compliance with good clinical practice and coordinating with partnering institutions.
  • Key responsibilities will include assisting with participant recruitment and enrollment, supporting data collection and management, maintaining study documentation, and ensuring adherence to study protocols and regulatory requirements.
  • The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, and a wide variety of professional development opportunities.

Matching Summary

The Clinical Research Coordinator B will manage phases of complex clinical trials under general supervision, ensuring compliance with good clinical practice and coordinating with partnering institutions.

Salary

$52,500.00 - $58,059.00 Annual Rate

Skills & Requirements

Must-have

  • manage phases of complex clinical trials
  • ensure compliance with good clinical practice
  • coordinate with partnering institutions
  • support monitoring of external sites
  • participate in study and protocol training
  • assist with participant recruitment and enrollment
  • support data collection and management
  • maintain study documentation
  • ensure adherence to study protocols
  • communicate with study participants
  • track study progress
  • prepare study materials and reports
  • supervise study research assistants
  • provide day-to-day oversight
  • lead study-related meetings
  • assist with IRB submissions and updates
  • support data quality assurance processes
  • contribute to study reporting
  • contribute to manuscript preparation
  • excellent interpersonal and communication skills
  • strong attention to detail
  • maintain accurate records
  • communicate effectively with diverse backgrounds
  • strong organizational skills
  • manage multiple tasks
  • meet deadlines
  • work collaboratively on a research team
  • interact with study participants
  • proficiency using computer programs for research operations
  • commit to diversity, equity, and inclusion

Nice-to-have

  • support the day-to-day study operations
  • evaluate the effects of healthy food policies
  • participate in Center-wide discussions
  • participate in journal clubs
  • participate in professional development trainings
  • experience with data analysis programs

Key Requirements

  • Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience
  • Master's degree is preferred
  • Proficiency using MS Office Suite, REDCap, Asana, email programs
  • Hybrid eligible

Work Rights

Not specified

Tailored Resume

Cover Letter