Clinical Research Coordinator- Neuropharmacology

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

DNRC Gengo Full Time Admin Amherst, NY, Amherst, NY, US

2 days ago Requisition

Salary Range: $22.00 To $28.00 Hourly

Dent Neurologic Institute is committed to excellence in all we do. Our culture is built on 4 key pillars: respect, quality, productivity, and well-being. By remaining dedicated to these values and the overall mission, we are dedicated to making a difference for both patients and colleagues. When you join the Dent team, you can take advantage of a variety of benefits

• Life Insurance
• 401(k) Retirement Plan
• Critical Illness, Accident, & Legal Plans
• Wellness Program
• Paid Time Off
• Paid Holidays
• Free Onsite Parking at All Locations

Location:

Amherst, NY
Position is FULLY ON-SITE.

Responsibilities include planning, organizing and implementing human subject research for the Dent Neurosciences Research Center according to the procedures set forth in research protocols. The Dent Neuroscience Research Center (DNRC) is a not-for-profit affiliate of DENT dedicated to outcomes research and education supported by foundations, industry and personal contributions. The DNRC is focused on developing comprehensive, clinically relevant, and cost-effective solutions to complex neurological problems faced in our community.

Building awareness, fostering relationships, providing support and continuous education are at the forefront of the DENT philosophy. From providing our patients with the most up-to-date diagnostic and treatment options for assisting each in the best care and coping opportunities, we aim to fulfill the needs of the whole patient. Through foundation support and exceptional faculty leadership, DNRC is able to build upon the philosophy by providing advancement, support, and education to our providers and partners.

Responsibilities of Position:

• Screens potential study subjects for possible protocol entry using inclusion and exclusion criteria.
• Explain specifics of research study, including requirements, medication, potential side effects, and medical care received or refers to investigator when appropriate.
• Explain testing procedures associated with study, including psychometric tests, and diagnostic or interventional procedures or refers to investigator when appropriate.
• Updates patients or subjects of current research study findings.
• Updates patients on results of study findings when completed.
• Interprets patient medical records, or refer to investigator where appropriate.
• Reviews laboratory/diagnostic tests or refer to investigator where appropriate.
• Identifies potential study candidates through review of physician appointment lists, patient medical records, and general advertisement.
• Performs study procedures, including subject interview, vitals, ECGs, and psychometric testing, and other required protocol tasks as delegated by the investigator and documents performance in source document and case record form.
• Updates database programs for study computers where appropriate, including patient randomization, correspondence, and hotline reports.
• Collects and documents data for research project, via the following:
• Creates and maintains case report forms along with summary sheets for convenient data analysis
• Creates labeling system for data collection
• Communicates with sponsor study monitor to ensure proper data collection as well as to gain feedback on how study is proceeding
• Establishes familiarity with various medical departments for collection of data (MRI films, CT, radiographs, etc.)
• Arranges schedules and appointments, including study subject visits, study staff schedule, and location of study…