Clinical Research Coordinator

Description The candidate will work as part of a team to initiate and manage research studies in the most optimal fashion. Ensure the accurate execution of research protocols in accordance with Good Clinical Practices, HIPPA and required obligations to patient/subject, Principal Investigator, research team and the sponsor. Directly interface with patients/subjects and the Principal Investigator in support of the clinical trials. Establish liaisons within the School of Medicine, and NYU Medical Center that may include: Research Nurses, Research Pharmacists, Program Managers, Medical Technicians, Clinical Information Systems, Regulatory Services such as IRB and selective departments.

Responsibilities:

* Thorough knowledge of research study, study rationale, study subject, and clinical procedures associated with the study.
* Recruitment capabilities and the screening of potential patients/subjects for eligibility to the study. This may include gathering information from the medical record, physician referral, advertisement and directly scheduling a visit to evaluate the patient/subject.
* Assist with the informed consent process and ensure that the patient/subject fully understands what is required of them throughout the study.
* Review all the elements of the screening process with the Principal Investigator that being: inclusion/exclusion criteria, completed informed consent, documentation of the event and the patient/subject willingness to participate in the study.
* Collaborate with various personnel that may be involved in assisting with specific aspects in the study.
* Interact with patient/subject and families in a courteous and professional manner. Be consistent and regularly follow through with your patient/subjects reminding them of visits and compliance. Extend this courteous and professional manner to staff within the School of Medicine and the Medical Center staff. Be cooperative at all times.
* Demonstrate knowledge of policies and procedures of the host institution where the study is being conducted and the regulatory requirements such as IRB and other approvals if necessary.
* Utilize available resources and established procedures to identify problems for quick resolution.
* Conduct study visits, obtain and document information within the time frame specified.
* Monitor any outward effects or issues regarding patient/subject safety and report this to the Principal Investigator, Physician and Research Nurse.

Requirements * Bachelor's degree plus one to two years related experience or equivalent combination of education and experience.
* Clinical Research Coordinator (CRC) Certification is preferred.