CLINICAL RESEARCH COORDINATOR I (3)

General Responsibilities

• Serve as coordinator for studies and provide support to other team members within the confines of the protocol as directed.
• Support screening and participant eligibility determination, working with more senior team members to ensure compliance.
• Conduct activities in accordance with the protocol, regulations, and Good Clinical Practice (GCP).
• To support the study life cycle from start-up to closure, including collecting and recording data, recruiting and performing follow-up with participants, scheduling visits, and assisting in coordination of lab and fieldwork.

Key Duties & Responsibilities

• Collects and documents data for clinical research programs.
• Recruits and performs follow-up with research participants as protocols outline.
• Schedules visits according to research protocols.
• Affords assistance in coordinating lab and fieldwork.
• Coordinates appointments for additional procedures as necessary.
• Prepares for and participates in study monitoring visits.
• Affords assistance in correcting findings.
• Participates in study meetings and conference calls.
• Affords assistance in completing Case Report Forms (CRF) according to protocol.
• Might afford assistance in the development of protocols and standard operating procedures (SOPs) for data.
• Performs administrative duties in support of research conduction as needed.
• Prepares source documentation for review with investigators.
• Might afford assistance in compiling, editing, and proofreading written reports for both internal and external administrative offices.
• Might use Electronic Data Capture (EDC) systems necessary for operations under supervision.
• Performs other duties as assigned.

Qualifications

• High School diploma or GED required.
• Two (2) years' experience with hands-on interaction, assessment, and treatment of patients, commonly found in hospitals and clinics.
• Knowledge of medical terminology, an understanding of medical technology, and electronic data capture experience.
• Knowledge of clinical trial processes, data collection, and data entry.
• Experience with recruiting and performing follow-up with research participants as protocols outline.
• Knowledge of protocols and standard operating procedures (SOPs) for data quality assurance.
• Must be able to walk 1.5 miles/day and lift 15 lbs.
• Knowledge of Microsoft Office products.
• Written and verbal communication skills.
• Data entry skills.