Clinical Research Coordinator

Conifer Health Solutions • Delray Beach, FL

1d • Onsite

About The Position

The Clinical Research Coordinator (CRC) will assist the Principal Investigator in the conduct of all aspects of the clinical trial, including regulatory tasks, under the direct supervision of the Clinical Research Manager and affiliated Director. The CRC provides operational support in the management of patients accrued to multiple research protocols to assure subjects’ safety and regulatory compliance.

Requirements

• AS Degree or higher level degree in Science, Healthcare, or a related field, to include graduate of foreign medical school.
• Must possess strong problem solving, analytical skills and process management skills.
• Must possess strong planning, organizational and project management skills, interpersonal and oral/written communication skills.
• Requires attention to detail and the ability to manage multiple priorities.
• Ability to work without close supervision or guidance and to exercise independent judgment.
• General PC skills.

Nice To Haves

• Two to three years of experience in clinical research to include healthcare compliance, research auditing, monitoring standards, or related experience.
• Knowledge of federal and state laws governing research preferred.
• Knowledge and understanding of both CPT and ICD-10 codes preferred.
• Experience with medical record documentation review for accuracy, and compliance with all laws, rules, policies and procedures preferred.

Responsibilities

• Coordinates study candidate testing and through the study screening, evaluation and enrollment process.
• Reviews testing with members of research study team to ensure criteria are met for inclusion or exclusion from the study.
• Follow up with patients that are interested in enrolling or are currently enrolled in clinical research studies and ensure compliance with the study protocol including reports of any unanticipated problems or serious adverse events.
• Utilizes information obtained throughout research study process, from screening, through exclusion from study or completion of study process with principal investigator and research team members with goal to provide optimal patient care.
• Assists with coordination of overall study management of participants.
• This includes patient’s care, reviewing potential study participants, appropriate testing, and following up on the results with principal investigator and research study team members.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree
• Number of Employees: 1,001-5,000 employees