Clinical Research Coordinator - Trials, Data & Study Visits

Jefferson Health Plans; Philadelphia (Philadelphia County); Presencial; USD 52.000 - 76.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical insurance

Tuition assistance

Retirement plans

Descripción de la vacante

Jefferson Health Plans is seeking aTemporary Clinical Research Coordinator to oversee the day-to-day activities of a clinical trial in line with Good Clinical Practice (GCP). The role includes data management, biospecimen processing, and assisting investigators with organizing and compiling research data.

Responsibilities include recruiting subjects, conducting study visits, and ensuring regulatory filings such as IRB submissions are completed.

Formación

• High School Diploma or GED and 4 years of relevant experience.
• Knowledge of and ability to utilize technology tools to organize, store and manage database systems.
• Knowledge of tools, techniques and processes for gathering and reporting data.
• Understanding of legislation and regulatory bodies affecting healthcare practices.
• Knowledge of patient rights and responsibilities.

Responsabilidades

• Oversee day-to-day activities of a clinical trial in accordance with GCP.
• Recruit and assist with consenting subjects and conduct study visits.
• Interact with staff to ensure adherence to research protocols and quality of information.
• Assist with regulatory filings including IRB submissions.
• May assist in enrollment of human subjects.

Conocimientos

Database management

Data gathering

Data reporting

Healthcare regulations

Patient rights

Multitasking

Educación

High School Diploma / GED

Descripción del empleo

Jefferson Health Plans is seeking aTemporary Clinical Research Coordinator to oversee the day-to-day activities of a clinical trial in line with Good Clinical Practice (GCP). The role includes data management, biospecimen processing, and assisting investigators with organizing and compiling research data.

Responsibilities include recruiting subjects, conducting study visits, and ensuring regulatory filings such as IRB submissions are completed.