Clinical Coordinator Jobs

About The Position

Requirements

• Bachelor’s degree with two years of clinical research experience, or an equivalent combination of education and experience.
• Experience in a medical and/or research setting.
• One year of clinical and/or survey research experience, including interviewing and supervising data collection procedures, or an equivalent combination of education and experience.
• Ability to travel to participant locations and collaborating institutions, locally, statewide, and nationally.
• Must complete CITI certification for Human Subject Research if not already completed.
• Complete all additional required WakeOne training for research coordinators.
• Strong judgment, organization, and communication skills.

Nice To Haves

• Master’s degree in public health, basic science, or a relevant clinical discipline.
• Phlebotomy license.
• Registered Record Administrator credential.
• SOCRA or ACRP certification.
• Paramedical or other clinical experience.
• Valid North Carolina driver’s license.

Responsibilities

• Assist with administration and coordination of all phases of assigned projects as directed.
• Ensure all aspects of the study are conducted according to the study protocol.
• Serve as the study liaison and representative.
• May train, direct, guide, and evaluate the work activities of other study personnel.
• Coordinate and participate in recruitment, data collection, and follow-up activities.
• Collect blood samples.
• Travel to collaborating institutions and participants’ homes locally, statewide, and nationally.
• Assist with developing data collection methods and creating or revising study materials, forms, manuals, and brochures.
• Prepare reports as requested.
• Provide guidance on or perform data processing, coordinate data analysis, and oversee data quality assurance.
• Order and maintain adequate project supplies.
• Initiate introductory visits according to study timeliness guidelines.
• Participate in outreach, community education, and early detection or screening events related to AD.
• Give presentations about AD and related dementias.
• Support IRB submissions, regulatory compliance, and study documentation.
• Prepare and ship research specimens, conduct participant visits, obtain informed consent, administer cognitive assessments, and gather family and medical histories.
• Perform other related duties incidental to the work described.

Benefits

• Paid Time Off programs
• Medical, dental, vision, life, and short- and long-term disability benefits
• Flexible Spending Accounts for eligible health care and dependent care expenses
• Adoption assistance and paid parental leave
• Defined contribution retirement plans with employer match
• Financial wellness programs
• Educational Assistance Program
• Career development programs