Clinical Research Coordinator

NY Scientific Corp. is a leading clinical research organization committed to advancing the future of medicine through the execution of innovative clinical trials. We are dedicated to driving the development of groundbreaking therapies by conducting high-quality research and providing crucial insights into experimental medications.

Role Summary:

We are seeking a highly motivated and experienced Clinical Research Coordinator to join our team in Brooklyn, NY. This full-time, on-site position will be responsible for the comprehensive coordination of clinical research activities, ensuring protocol adherence, managing informed consent processes, and overseeing the day-to-day operations of clinical trials.

Responsibilities:

• Coordinate and manage research activities under the supervision of the Principal Investigator (Licensed MD) and Site Director.
• Review, extract, and analyze data from medical charts to identify potential subjects and assess eligibility.
• Assess protocol inclusion/exclusion criteria to confirm subject eligibility for participation in clinical studies.
• Recruit and interview prospective subjects for clinical studies, ensuring a thorough understanding of the research objectives and requirements.
• Manage patient visits, providing exceptional care and attention to ensure a positive participant experience.
• Perform essential clinical procedures, including phlebotomy, ECGs, pulmonary function tests, and blood pressure measurements.
• Maintain meticulous records and documentation in compliance with Good Clinical Practice (GCP) guidelines and FDA regulations.
• Utilize various Electronic Data Capture (EDC) formats for data entry and management.

Qualifications:

• Bachelor's degree in a related field; Master's degree preferred.
• Minimum of 1 year of experience as a Clinical Research Coordinator, demonstrating a proven track record in conducting multiple clinical trials.
• Comprehensive understanding of informed consent processes and protocol management.
• Demonstrated experience in clinical research and clinical trials.
• Thorough knowledge of GCP guidelines and FDA regulations.
• Proficiency in utilizing various EDC formats for data management.
• Current GCP and IATA certification required.
• Exceptional attention to detail and organizational skills.
• Excellent interpersonal and communication skills, with the ability to effectively interact with patients, colleagues, and stakeholders.
• Proven ability to work collaboratively within a team environment.
• Must be hardworking, meticulous, and detail-oriented.
• Must be able to provide three professional references.

To Apply:

• Interested candidates are encouraged to submit their resume and cover letter for consideration.