Clinical Research Coordinator I - Radiation Oncology

Washington University in St Louis • Forest Park, GA

1d • Onsite

About The Position

This position assists investigators as coordinator of a basic to moderately complex clinical research study. The role may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community, and study participants. The primary responsibility is managing and recording all phases of study protocol as required by the sponsoring agency to ensure compliance.

Requirements

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• Basic Life Support - American Heart Association, Basic Life Support - American Red Cross
• Basic Life Support certification must be obtained within one month of hire date.
• Basic Life Support certification (Online Basic Life Support certifications, those without a skills assessment component, are not sufficient to meet the Basic Life Support requirements).

Nice To Haves

• Clinical Research
• Clinical Study Protocols
• Communication
• Computer Systems
• Interpersonal Communication
• Organizing
• Research Support

Responsibilities

• Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies.
• Establishes record-keeping systems.
• Makes assessments and determinations of participants’ progress in the study.
• Analyzes, investigates and reports adverse events.
• Makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants.
• Resolves protocol management issues and recommends corrective action as appropriate.
• Serves as liaison with funding or sponsoring agency.
• Recruits and enrolls study participants.
• Makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews.
• Develops informed consent packets for study participants and confers with participants to explain the purpose of the study and obtain completed informed consent packets.
• Explains diagnostic procedures and treatment plans to address participant/family concerns.
• Administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
• Ensures timely completion of all protocol requirements (assessment, lab testing, procedures and treatments), to include scheduling and facilitating the patient’s timely completion of protocol requirements.
• Evaluates and interprets collected clinical data as appropriate.
• Prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.
• Collects clinical data under clinical research protocols.
• Performs other duties as assigned.

Benefits

• Up to 22 days of vacation, 10 recognized holidays, and sick time.
• Competitive health insurance packages with priority appointments and lower copays/coinsurance.
• Free Metro transit U-Pass for eligible employees.
• 4 weeks of caregiver leave to bond with your new child.
• Family care resources are also available for your continued childcare needs.
• Adult care resources.
• Tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years with us.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level