Clinical Science Research Professional
About the position Responsibilities • Assist with and oversee the day-to-day operations of clinical trials and studies. • Obtain study subjects' medical history and current medication information, review research protocol inclusion/exclusion criteria, and confirm eligibility of subjects to participate in clinical trials. • Perform informed consent process or ensure that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required. • Interview prospective subjects for a variety of research clinical trials and educate them on the details of the studies through phone contacts and personal interviews. • Schedule subject participation in research clinical trials, coordinating availability of necessary space and clinical research support. • Collect, code, and analyze data obtained from research in an accurate and timely manner. • Adhere to research regulatory standards and maintain detailed records of studies to ensure compliance with FDA and other regulatory guidelines. • Participate in subject recruitment efforts, including communicating with patients expressing interest and all pre-screening/screening activities. • Ensure that the necessary supplies and equipment for studies are in stock and in working order. • Independently master study materials, including protocols and informed consent forms for assigned studies. • Independently perform study-related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies. • Assist Team Leads, Supervisors, and/or management with creation and implementation of processes and procedures and quality improvement initiatives. • Act as a Primary Coordinator on multiple trials/studies and assist and train junior team members. Requirements • Bachelor's degree in any field. • A combination of education and related technical/paraprofessional experience may be substituted for the bachelor's degree on a year-for-year basis. • One (1) year clinical research or related experience. Nice-to-haves • One (1) year experience recruiting study participants for clinical trials. • Bachelor's degree in science or health-related field. • Two (2) years of clinical research or related experience. • One (1) year experience with electronic data capture systems (e.g., EMR or EHR and data management systems). • One (1) year of experience using REDCap. • Experience with OB/GYN or sexual and reproductive health research. • Experience as a project manager. • Fluent in Spanish and able to pass an interpreter exam. • Phlebotomy certification. Benefits • Health insurance • Life insurance • Retirement plan • Tuition reimbursement • Paid time off Apply tot his job Apply tot his job