Clinical Trials Support Specialist
: Job Details :

Clinical Trials Support Specialist

Full-Time: Mon-Fri

THE BEST CAREERS. RIGHT HERE

@ BROOKLYN'S LEADING HEALTHCARE SYSTEM.

MAIMONIDES: TOP TEN IN THE U.S. FOR CLINICAL OUTCOMES

We're Maimonides Health, Brooklyn's largest healthcare system, serving over 250,000 patients each year through the system's 3 hospitals, 1800 physicians and healthcare professionals, more than 80 community-based practices and outpatient centers. At Maimonides Health, our core values H.E.A.R.T drives everything we do. We uphold and maintain Honesty, Empathy, Accountability, Respect, and Teamwork to empower our talented team, engage our respective communities and provide patient-centered care. The system is anchored by Maimonides Medical Center, one of the nation's largest independent teaching hospitals and home to centers of excellence in numerous specialties; Maimonides Midwood Community Hospital (formerly New York Community Hospital), a 130-bed adult medical-surgical hospital; and Maimonides Children's Hospital, Brooklyn's only children's hospital and only pediatric trauma center. Maimonides' clinical programs rank among the best in the country for patient outcomes, including its Heart and Vascular Institute, Neurosciences Institute, Bone and Joint Center, and Cancer Center. Maimonides is an affiliate of Northwell Health and a major clinical training site for SUNY Downstate College of Medicine.

We currently have a unique full-time opportunity for a Clinical Trials Support Specialist in our Cancer Center Administration Department. In this role, you will:

• Prepare, submit, and maintain IRB documents, as well as maintain the site Trial Master file, delegation logs and all other essential documents.
• Screen patients for enrollment into clinical research studies and enroll patients in studies. Take part with the PI in the informed consent discussion process and documentation of informed consent.
• Educate participants regarding study requirements and help them complete the required study procedures.
• Monitor progress of subject recruitment. Report adverse events on RAVE at the end of every treatment cycle after discussion with the Principal Investigator.
• Coordinate participant tests and visits. Assist the physicians in conducting the patient visits.
• Collect Research samples per protocol during the patient visits and ship them as per IATA/DOT standards. Keep track of shipments until they are delivered. Maintain inventory of study kits.
• Organize and maintain study files including regulatory binders, study specific source documentation and other materials.
• Perform data collection from electronic medical health records and data submission to databases in a timely fashion. Respond to data queries from the study monitor.
• Perform study surveys with the patients and collect and maintain the study data.

We require:

• Bachelor's of Science in Biology or Chemistry; Master's preferred.
• 2 years of research experience in the medical field or an advanced degree in Biology or Chemistry.

Salary: $66,779. We offer comprehensive benefits including 403(b) retirement plan. For immediate consideration, please forward a resume/CV to: ...@maimo.org

Maimonides Medical Center (MMC) is an equal opportunity employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard for race, creed (religion), color, sex, national origin, ethnicity, sexual orientation, gender identity, military or veteran status, age, disability, pregnancy, predisposing genetic characteristic, marital status or domestic violence victim status, citizenship status, or any other factor which cannot lawfully be used as a basis for an employment decision in accordance with applicable federal, state, and local laws. MMC is committed to following the requirements of the New York State Human Rights Law with regard to non-discrimination on the basis of prior criminal conviction and prior arrest.