Clinical Research Coordinator
Behavioral Health Market Context
Apply Nowvia Tenet Health - Tenet Healthcare Corporation
Benefits
That’s why we offer more than a job – we provide a comprehensive benefit package that prioritizes your health, professional development, and work-life balanceMedical, dental, vision, and life insurance401(k) retirement savings plan with employer matchGenerous paid time offCareer development and continuing education opportunitiesHealth savings accounts, healthcare & dependent flexible spending accountsEmployee Assistance program, Employee discount programVoluntary benefits include pet insurance, legal insurance, accident and critical illness insurance, long term care, elder & childcare, auto & home insurance5 more items(s)
Qualifications
- •AS Degree or higher level degree in Science, Healthcare, or a related field, to include graduate of foreign medical school
- •Minimum: 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
- •Two to three years of experience in clinical research to include healthcare compliance, research auditing, monitoring standards, or related experience
- •4 more items(s)
Responsibilities
- •The Clinical Research Coordinator (CRC) will assist the Principal Investigator in the conduct 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
- •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
- •5 more items(s)
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