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Washington University of St. Louis Clinical Research Coordinator I - Ob/Gyn - 51784 in St. Louis, Missouri

Job Type/Schedule This position is full-time and works approximately 40 hours per week. Department Name/Job Location This position is in the Department of Ob/Gyn. This position is for the Medical School Campus. Essential Functions POSITION SUMMARY: This position will work with the existing clinical and research staff of the Family Planning Division and the Contraceptive Choice Center (C3). C3 is a Title-X funded family planning clinic which provides care to a diverse patient population including low-income and uninsured patients. The Clinical Research Coordinator will work with the C3 team to perform data analysis and reporting. In addition, the Clinical Research Coordinator will assist with budget drafting and grant writing. The Clinical Research Coordinator will also be responsible for coordinating new and existing family planning related research studies, including IRB application, recruitment, enrollment, administration of surveys and other research procedures, and regulatory compliance. PRIMARY DUTIES AND RESPONSIBILITIES: 1. Routinely 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 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 IRB/protocol management issues and recommends corrective action as appropriate; serves as liaison with the study sponsor; works closely with the sponsor CRAs both remotely and during in-person site visits by responding to data queries, discussing issues as they arise, and attending study FAQ calls. 2. Routinely 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 purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; routinely 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. 3. Routinely extracts clinical data from the electronic medical record, performs basic data analysis, and assists with financial reporting for C3; prepares oral or written presentations or reports and analyses setting forth progress trends. 4. Performs other duties incidental to the work described herein. Required Qualifications Bachelor’s degree required; prior work experience, preferably in clinical research support, is highly preferred; a combination of relevant work and education equaling four years may substitute for this requirement. Preferred Qualifications * Master’s degree in social work, public health, psychology, or related field. * Clinical research and data management experience. * Effective communication skills and an interest in reproductive health. * Strong critical thinking skills, capacity for detailed record keeping, and working knowledge of computer programs and basic data analysis. * Ease and comfort discussing reproductive health issues and familiarity with scientific and medical terminology. Salary Range The hiring range for this position is $43,326 - $54,204 annually. Pre-Employment Screening All external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. Current employees applying for a new position within the university may be subject to this requirement. The screenings will include a criminal background check and, as applicable for the position, other background checks, drug screen, employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. All offers are contingent upon successful completion of required screening. Benefits This position is eligible for full-time benefits. Please click the following link to view a summary of benefits: https://wustl.box.com/s/8wkhs25yssf0775x9d6nd6vqa7obpth7. EOE Statement Washington University is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, genetic information, disability, or protected veteran status. Job Title: Clinical Research Coordinator I - Ob/Gyn - 51784 Job ID: 51784 Location: Medical School Full/Part Time: Full-Time Regular/Temporary: Regular

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