Clinical Research Coordinator
On-site · Philadelphia, Pennsylvania, United States
Job Summary
Clinical Research Coordinator responsible for day-to-day oversight of a clinical trial in accordance with Good Clinical Practice (GCP). Works on database management, biospecimen processing, and clerical duties to assist investigators in organizing, gathering, and compiling clinical research data. Recruits, assists with consenting subjects, and conducts study visits. Interfaces with Principal Investigator and regulatory bodies to ensure adherence to protocols and quality information; maintains documentation required for trials; supports IRB submissions and potential subject enrollment.
Required Qualifications
- High School Diploma/GED or equivalent
- 4 years of relevant experience
- Knowledge of technology tools to organize, store and manage database systems
- Knowledge of tools, techniques and processes for gathering and reporting data
- Knowledge and understanding of legislation and regulatory bodies affecting healthcare practices
- Ability to manage multiple concurrent objectives, projects, groups, or activities, making effective judgments as to prioritizing and time allocation
- Lift and carry 40-50 lbs. including patient transport scenarios
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