Pulmonary Clinical Research Coordinator — Impactful Trials

Jefferson Health; Philadelphia (Philadelphia County); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Retirement plans

Tuition assistance

Flexible spending accounts

Job summary

Jefferson Health in Philadelphia is seeking a Clinical Research Coordinator to oversee day-to-day trial activities in our pulmonary research program. You will manage data, biospecimen processing, and clerical tasks to support investigators and ensure compliant study conduct.

The role includes recruiting and consenting subjects, coordinating study visits, and assisting with regulatory filings and enrollment as needed. A strong understanding of GCP and data management is essential.

Qualifications

• High School Diploma/GED or equivalent.
• 4 years of relevant clinical research experience.
• Knowledge of and ability to utilize technology tools to organize and manage databases.
• Understanding of healthcare regulatory requirements.
• Ability to manage multiple objectives with prioritization.

Responsibilities

• Interacts with co-workers, visitors, and staff consistent with Jefferson values.
• Performs research, data base, biospecimen collection and processing to assist investigators.
• Organizes and maintains documentation required for clinical trials.
• Informs Principal Investigator of patient responses to treatment and adverse effects when present.
• Assists Principal Investigator with IRB submissions and regulatory filings.
• May assist in enrollment of human subjects.
• Provides clerical and technical support to ensure adherence to research protocols.

Skills

Clinical research

GCP knowledge

Data management

Regulatory compliance

Multitasking

Education

High School Diploma/GED

Job description

Jefferson Health in Philadelphia is seeking a Clinical Research Coordinator to oversee day-to-day trial activities in our pulmonary research program. You will manage data, biospecimen processing, and clerical tasks to support investigators and ensure compliant study conduct.

The role includes recruiting and consenting subjects, coordinating study visits, and assisting with regulatory filings and enrollment as needed. A strong understanding of GCP and data management is essential.