Clinical Science Research reputed company

About the position The Clinical Science Research reputed company will support the Fertility Preservation and Reproductive Late Effects (FPRLE) program reputed company the Department of Obstetrics and Gynecology at the reputed company. This full-time position involves assisting the research team in conducting clinical and community-based research reputed company on fertility and reproductive health. The role requires a strong understanding of biological and medical sciences, excellent communication skills, and the ability to work in a high-intensity research environment. Responsibilities • Assist with and reputed company the day-to-day operations of reputed company and studies. • Obtain study subjects' medical history and reputed company medication information, review research protocol inclusion/exclusion reputed company, and confirm eligibility of subjects to participate in reputed company. • reputed company informed consent process or ensure that the informed consent process has occurred, is properly documented, and that informed consent reputed company documents are filed as required. • Interview prospective subjects for a reputed company of research reputed company and reputed company them on the details of the studies through phone contacts and personal interviews. • Schedule subject participation in research reputed company, coordinating availability of necessary reputed company and clinical research support. • Collect, reputed company, and analyze data obtained from research in an accurate and reputed company 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 reputed company reputed company-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 reputed company study-reputed company 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 reputed company improvement initiatives. • reputed company 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 reputed company technical/paraprofessional experience may be substituted for the bachelor's degree on a year-for-year reputed company. • One (1) year clinical research or reputed company experience. reputed company-to-haves • One (1) year experience reputed company study participants for reputed company. • Bachelor's degree in science or health-reputed company field. • Two (2) years of clinical research or reputed company 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 reputed company to pass an interpreter exam. • Phlebotomy certification. Benefits • Health insurance • Life insurance • Retirement plan • Tuition reimbursement • reputed company time off Apply tot his job Apply To this Job