Clinical Research Coordinator, HSS Center for Regenerative Medicine

How you move is why we’re here. ® Now more than ever. Get back to what you need and love to do. The possibilities are endless... Now more than ever, our guiding principles are helping us in our search for exceptional talent - candidates who align with our unique workplace culture and who want to maximize the abundant opportunities for growth and success.

If this describes you then let’s talk! HSS is consistently among the top-ranked hospitals for orthopedics and rheumatology by U.S. News & World Report. As a recipient of the Magnet Award for Nursing Excellence, HSS was the first hospital in New York City to receive the distinguished designation. Whether you are early in your career or an expert in your field, you will find HSS an innovative, supportive and inclusive environment.

Working with colleagues who love what they do and are deeply committed to our Mission, you too can be part of our transformation across the enterprise.

Emp Status Regular Full time Work Shift Day (United States of America)

Compensation Range The base pay scale for this position is $0.00 - $0.00. In addition, this position will be eligible for additional benefits consistent with the role. The salary of the finalist selected for this role will be determined based on various factors, including but not limited to: scope of role, level of experience, education, accomplishments, internal equity, budget, and subject to Fair Market Value evaluation.

The hiring range listed is a good faith determination of potential compensation at the time of this job advertisement and may be modified in the future.

Integrated in the Center for Regenerative Medicine (CRM), the Clinical Research Coordinator will work closely with Sports Medicine physicians (Principal Investigators) and will directly report to the AVP, Clinical Operations Officer and Chief Pharmacy Officer. Responsible for all aspects of clinical research studies including but not limited to, screening and enrolling patients following inclusion/exclusion criteria, collecting biospecimens both in the office setting and the OR, data management activities while assuring compliance with protocols and ICH GCPs, assisting with protocol development, submitting new and continuing review to the IRB, and coordinating clinical and lab activities to integrate all protocol activities.

The CRC will be in compliance with all regulatory, institutional, and departmental requirements; maintains regulatory binders, liaises with communications and preparation of documents for the FDA; participates in all aspects of research management and quality assurance of data for the Principal Investigator. The successful applicant for the position of Clinical Research Coordinator will be a highly motivated and organized individual who is able to perform a variety of different tasks essential to the implementation and successful completion of a clinical study.

He or she should be knowledgeable of regulations regarding Human Subjects research and assure HIPAA compliance. The applicant must be able to multitask and prioritize research projects. A qualified candidate will have the ability to communicate in an effective manner with management, clinical staff, external sponsors and patients  candidate will also have good interpersonal and writing skills, as he or she will interface directly with patients and medical staff on a routine basis.

He or she will be flexible, as the job description may evolve as studies progress. The applicant must be available on site at the main hospital.

Oversees and conducts the informed consent process on studies as appropriate (requires appropriate training and certification of human research subjects training). Manages data collection specific to research studies including but not limited to the performance of measurements for applicable studies, collection of clinical data from patients directly, and manages the performance of all other duties as put forth in the protocol.

This includes collaboration with multidisciplinary teams involved in the successful initiation and conduct of clinical research…