CLINICAL RESEARCH COORDINATOR I (PART-TIME) (DEMOPOLIS, AL)

General Responsibilities

To collect and record preliminary data for clinical research programs.

To recruit and perform follow-up with research participants as protocols outline.

To schedule visits according to research protocols.

To assist in coordination of lab and fieldwork.

To maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations.

Key Duties & Responsibilities

• Serves as coordinator for studies and initiatives and provides support to other team members within the confines of the protocol as directed.
• Supports screening and participant eligibility determination, consent, enrollment, survey, and provides health education and navigation services.
• Conducts activities in accordance with the protocol, regulations and Good Clinical Practice (GCP).
• Affords assistance to the study life cycle from start-up to closure, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits, and assisting in the coordination of lab and fieldwork.
• Performs other duties as assigned.

Qualifications

• High School diploma or GED required.
• Ability to operate various office machines, including printers, computers, and various software packages.
• Interpersonal skills.
• Knowledge of Microsoft Office products.
• Written and verbal communication skills.
• Data entry skills.