Clinical Trials Coordinator II: Data, Recruiting & Compliance

Jefferson Health; Philadelphia (Philadelphia County); Sur place; USD 45 000 - 65 000; Plein temps

Avantages offerts par ce poste

Medical Insurance

Tuition assistance

Retirement plans

Résumé du poste

Thomas Jefferson University in Philadelphia, PA, seeks a Clinical Research Support role to oversee daily trial activities under GCP, manage data, and assist investigators in collecting and organizing clinical research data.

Responsibilities include regulatory filings, patient consent support, study visits, and potential enrollment assistance, with a focus on accurate documentation and compliant procedures.

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 legislation and regulatory bodies affecting healthcare practices.
• Ability to manage multiple concurrent objectives, projects, groups, or activities.

Responsabilités

• Interacts with co-workers, visitors, and other staff consistent with Jefferson values.
• Performs research activities for clinical trials including database management and biospecimen processing.
• Organizes and maintains documentation required for clinical trial(s).
• Informs Principal Investigator and/or designated individual on any issues concerning patients. response to treatment/adverse effects.
• Assists Principal Investigator with regulatory filings including IRB submissions.
• May assist in the enrollment of human subjects.

Connaissances

GCP knowledge

Database management

Regulatory knowledge (IRB)

Data collection/processing

Clerical duties

Formation

High School Diploma/GED or equivalent

Outils

Database software

Description du poste

Thomas Jefferson University in Philadelphia, PA, seeks a Clinical Research Support role to oversee daily trial activities under GCP, manage data, and assist investigators in collecting and organizing clinical research data.

Responsibilities include regulatory filings, patient consent support, study visits, and potential enrollment assistance, with a focus on accurate documentation and compliant procedures.