The Research Associate oversees multiple clinical trials, ensuring adherence to study protocols, regulatory requirements, and seamless daily trial activities. They coordinate team members, manage patient recruitment and assessments, and handle IRB documentation and billing processes.
Requirements summary
Candidates must hold a Bachelor's degree and have completed GCP training. A record of clinical research publications and proficiency in MS Office are required, along with strong communication and organizational skills.
bachelor degreeMS OfficeLeadershipCommunication skillsAttention to detailProject managementElectronic medical recordsRegulatory complianceData entryClinical assessmentsProtocol adherenceInformed consentPatient recruitmentClinical trialsWorkflow developmentIRB submissionGCP training
Job description
City/State
Bronx,
New
York
Grant
Funded:
Yes
Department:
Card -
Cardiology
Research
Work
Shift:
Day
Work
Days:
MON-FRI
Scheduled
Hours: 8:30
AM-5
PM
Scheduled
Daily
Hours: 7.5
HOURS
Pay
Range: The Research Associate 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 - Directing 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. - Directing strict adherence to the study protocols, as well as sponsor, FDA and other regulatory authority requirements. - Developing workflows for clinical trial, including reminders/updates to the clinical team. - Coordinating 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.
Prepares and submits all protocol applications, amendments, continuing reviews, and informed consent documents for IRB review and approval. - Executing patient billing in multiple databases including the patient’s electronic medical record. - Developing action plans for ensuring all study tasks are completed as required per the protocol and developing subsequent corrective action plans if any errors are made.
Coordinates assigned study monitoring and auditing visits with study coordinator, investigator, industry sponsors, and internal/external auditors. The Research Associate will be trained to be highly specialized in clinical trials assigned to them and is expected to be able to manage clinical trial projects independently after sufficient training is completed
Benefits
Discount programs
Insurance products
QUALIFICATIONS: Bachelors Degree required GCP training required A 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 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. Calling All Nurses!
Nurse
Recruitment
Hotline: 718-920-6697;
Monday-Friday: 9am-4pm Since its inception in 1884, Montefiore’s mission has been to heal, to teach, to discover and advance the health of the communities we serve. Montefiore's state-of-the-art facilities include the internationally-recognized Children’s Hospital at Montefiore and our Notable Centers of Excellence - Montefiore Einstein Center for Cancer Care, Montefiore Einstein Center for Heart and Vascular Care, Montefiore Einstein Center for Transplantation. Combined with a growing number of locations for primary and specialty care throughout the Bronx and Westchester County, Montefiore is the ideal organization to apply and hone your expertise. An assortment of insurance products and discount programs through Voluntary Benefits. Check out our comprehensive benefits available to you when you join our outstanding team! To heal, to teach, to discover and to advance the health of the communities we serve. To be a premier academic medical center that transforms health and enriches lives. Automated Employment Decision Tools Notice (AEDT)
