Research Associate I

City/State: Bronx, New York – Grant Funded: Yes – Department: Card-research Administration – Work Shift: Day – Work Days: MON-FRI – Scheduled Hours: 8:30AM‑5PM – Scheduled Daily Hours: 7.5HOURS – Pay Range: $53,040.00‑$66,300.00 The Research Associate I will oversee multiple clinical trials, serving as a point person for patients, their family members, and the clinical study team. The position consists of working with various departments across the hospital, including forging new partnerships with departments to ensure completion of trial‑related activities. The clinical research coordinator I will direct participants and study team members to adhere to the study protocol and rules and regulations governed by regulatory bodies including Institutional Review Boards and the FDA. Job Responsibilities Direct seamless flow of daily trial‑related activities, including data entry, consent and recruitment and clinical assessments as required by the study protocol of the study subjects. Direct strict adherence to the study protocols, as well as sponsor, FDA and other regulatory authority requirements. Develop workflows for clinical trial, including reminders/updates to the clinical team. Coordinate team members to complete both clinical and non‑clinical assessments per protocol. This includes developing workflow for patient care such as assigning secretaries to schedule patients, developing workflow with ancillary departments (such as radiology, advanced imaging, pathology, pharmacy), and assigning appropriate clinical team members such as doctors to complete clinical tasks such as reviewing adverse events versus assigning non‑clinical team members to complete non‑clinical tasks such as administering questionnaires to a patient. Prepare and submit all protocol applications, amendments, continuing reviews, and informed consent documents for IRB review and approval. Execute patient billing in multiple databases including the patient’s electronic medical record. Develop action plans for ensuring all study tasks are completed as required per the protocol and develop subsequent corrective action plans if any errors are made. Coordinate assigned study monitoring and auditing visits with study coordinator, investigator, industry sponsors, and internal/external auditors. Qualifications Bachelor’s Degree required GCP training required Record of clinical research publication from prior research work MS Office proficient Excellent written and oral communication skills Exceptional attention to detail and accuracy Ability to manage multiple tasks & priorities Demonstrated leadership potential Knowledge of a variety of concepts, practices and procedures in directly related field Montefiore Medical Center is an equal employment opportunity employer. Montefiore Medical Center will recruit, hire, train, transfer, promote, layoff and discharge associates in all job classifications without regard to their race, color, religion, creed, national origin, alienage or citizenship status, age, gender, actual or presumed disability, history of disability, sexual orientation, gender identity, gender expression, genetic predisposition or carrier status, pregnancy, military status, marital status, or partnership status, or any other characteristic protected by law. #J-18808-Ljbffr