Clinical Trial Coordinator & Data Specialist

Jefferson; United States; On-site; USD 55,000 - 80,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Life Insurance

Disability insurance

Retirement plans

Tuition assistance

Flexible spending accounts

Job summary

Jefferson in Philadelphia seeks a Clinical Research Associate to oversee the day-to-day activities of a clinical trial under GCP, including data management, biospecimen processing, and study visits.

You will recruit subjects, assist with consent, ensure regulatory filings, and maintain trial documentation. This temporary role supports investigators and requires strong organizational skills and the ability to manage multiple tasks.

Qualifications

• High School Diploma or GED required.
• 4 years of relevant experience.
• Knowledge of technology tools to organize, store and manage database systems.
• Knowledge of data collection and reporting in a department or division.

Responsibilities

• Interact with co-workers, visitors, and staff per Jefferson values.
• Support clinical trials with research, data base, biospecimen collection and processing, and clerical duties.
• Organize and maintain documentation for clinical trials.
• Inform PI of issues related to patient response to treatment or adverse effects.
• Assist PI with regulatory filings including IRB submissions.
• May assist in enrollment of human subjects.
• Provide clerical and technical support to ensure adherence to protocols.

Education

High School Diploma/GED or equivalent

Job description

Jefferson in Philadelphia seeks a Clinical Research Associate to oversee the day-to-day activities of a clinical trial under GCP, including data management, biospecimen processing, and study visits.

You will recruit subjects, assist with consent, ensure regulatory filings, and maintain trial documentation. This temporary role supports investigators and requires strong organizational skills and the ability to manage multiple tasks.