Research Coordinator-Personalized Medicine

Nevada System of Higher EducationEvanston, IL
82d$24 - $37

About The Position

The Research Coordinator for Personalized Medicine will be responsible for providing clinical care services, including consenting, treating, and monitoring patients. The role involves recruiting and screening candidates for clinical trials, acquiring past medical and medication history profiles, shipping lab samples, and dispensing research drugs to patients according to protocol. The coordinator will utilize electronic capture to update patient information and help oversee clinical data for audits and oversight visits. Additionally, the position requires performing a variety of research, data entry, and regulatory duties related to departmental research endeavors, ensuring adherence to protocols and quality of information received. The coordinator will identify and screen study participants, enroll subjects in trials, assist with budget proposals and study budget tracking, ensure compliance with regulations for the protection of human subjects, complete regulatory submissions for the Institutional Review Board (IRB), and communicate with physicians and other departmental personnel as required for study design and implementation. The role also includes completing data abstraction and timely reporting of study-related adverse events to the sponsor.

Requirements

  • Bachelor’s degree required, in the fields of social, biological or healthcare sciences preferred
  • 1-5 years of research experience
  • Experience with phlebotomy, ECG and pharmacy practices preferred

Responsibilities

  • Provides clinical care services including consenting, treating and monitoring of patients
  • Recruit and screen candidates for clinical trials
  • Acquire past medical and medication history profiles
  • Ship lab samples
  • Dispense research drug to patients according to protocol
  • Utilize electronic capture to update patient information
  • Helps to oversee clinical data for audits and oversight visits
  • Perform a variety of research, data entry and regulatory duties related to departmental research endeavors
  • Ensure adherence to protocols and quality of information received
  • Identifying and screening study participants, enroll subjects to the trials in adherence with the protocol
  • Assist with budget proposals and study budget tracking
  • Assist with study time reporting
  • Ensure compliance with local, state and Federal regulations for the protection of human subjects
  • Complete regulatory submissions/revisions for the Institutional Review Board (IRB)
  • Communicate and coordinate with physicians, division staff, and other departmental study personnel as required for study design, implementation and completion
  • Complete data abstraction and data entry for study specific databases
  • Review and timely report study related adverse events to the sponsor

Benefits

  • Career Pathways to Promote Professional Growth and Development
  • Various Medical, Dental, and Vision options
  • Tuition Reimbursement
  • Free Parking at designated locations
  • Wellness Program
  • Savings Plan
  • Health Savings Account Options
  • Retirement Options with Company Match
  • Paid Time Off and Holiday Pay
  • Community Involvement Opportunities
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