Clinical Research Coordinator: Trials & Data Support

Jefferson; United States; On-site; USD 52,000 - 75,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Retirement plans

Job summary

Jefferson in Philadelphia is seeking a Clinical Research Coordinator to oversee the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). You will support investigators with data collection, biospecimen processing, consents, and study visits.

The role involves regulatory filings, enrollment support, and maintaining trial documentation in a collaborative healthcare environment.

Qualifications

• Education: Minimum High School Diploma or equivalent.
• AND Experience: High School Diploma or equivalent and 4 years of relevant experience or bachelor’s degree/master’s degree and previous experience preferred.
• Location: 1015 Chestnut Street, Philadelphia, Pennsylvania, United States of America.

Responsibilities

• Interacts with co-workers, visitors, and other staff consistent with the values of Jefferson.
• Performs a variety of research, data base, biospecimen collection and processing, as well as clerical duties in support of clinical trials to assist investigators in organizing, gathering and compiling clinical research data.
• Organizes and maintains documentation required for clinical trial(s).
• Informs Principal Investigator and/or designated individual on any issues concerning patients' response to treatment/medication/ any adverse effects overall to patients.
• Assists Principal Investigator with regulatory body filings including IRB submissions.
• May assist in the enrollment of human subjects.
• May provide clerical and technical support to ensure adherence to research protocols and quality of information received.

Job description

Jefferson in Philadelphia is seeking a Clinical Research Coordinator to oversee the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). You will support investigators with data collection, biospecimen processing, consents, and study visits.

The role involves regulatory filings, enrollment support, and maintaining trial documentation in a collaborative healthcare environment.