Job description

Clinical Research Coordinator
CLINICAL RESEARCH COORDINATOR

POSITION SUMMARY:

This position is a short-term position (6 months) with the possibility of extending another few months and even long-term. We have an over-night study which will require the coordinator, along with a Registered Nurse, to provide care for 1 to 4 patients at a time (3 night stay). We are hiring for 2 shifts (night shift 7pm-7am) and Day Shift (7am-7pm). We have two locations (St. Louis and O'Fallon, IL). The overnight stay may occur at either location. If the overnight for that week is at the St. Louis office, then the shift will be: Monday, Tuesday and Wednesday. If the stay is in our O'Fallon, IL office, the shift would be Friday, Saturday and Sunday. We can discuss your preference in the interview.

We will consider candidates looking for either full-time or a part-time position.

PRIMARY DUTIES AND RESPONSIBILITIES:

• Plans, schedules and coordinates detailed phases of Phase 1b, Phase 2, Phase 3 and Phase 4 research studies.
• Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies problems and/or inconsistencies and monitors participants progress to include documentation and reporting of adverse events.
• Compiles and enters the data from the study visits
• Complete and maintain source documentation and case report forms according to project requirements Assist with maintenance of study file documentation. Participate in monitor visits and audits.
• Develop and maintain rapport and open communication with subjects and their families of diverse age, social background, and mental or physical status. Provide follow-up with subjects and their families to enhance adherence to study protocols and to provide opportunities for subjects and their families to ask questions regarding the study, study medication and treatment, or general health care.
• Evaluates and interprets collected clinical data in conjunction with PI as appropriate.
• Collects clinical data under clinical research protocols, enters the data in the EDC in a timely fashion and responds to queries.
• Performs other duties as assigned.

KNOWLEDGE, SKILLS, ABILITIES, AND PERSONAL CHARACTERISTICS

• Knowledge of specialized medical/scientific terminology
• Knowledge of medication and proper dosages
• Ability to maintain confidentiality.
• Ability to type quickly and be well versed in EMR systems.
• Above average verbal, written, and interpersonal communication skills.
• Capable of relating to diverse age and demographic backgrounds.
• Demonstrate diplomacy, tact and professional demeanor.
• Possess organizational skills, analysis, supervision, and prioritization abilities.

Job Types: Full-time, Part-time

Pay: $25.00 - $30.00 per hour

Schedule:

• 12 hour shift
• Day shift
• Overnight shift

Supplemental pay types:

• Bonus pay

Education:

• Bachelor's (Preferred)

Experience:

• Clinical research: 1 year (Required)

Work Location: In person

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