Alzheimer's Research Coordinator – Outreach & Data

Hugh Chatham Health, Inc.; Winston-Salem (NC); Presencial; USD 37 000 - 55 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Paid Time Off

Health benefits

Educational Assistance

Resumo da oferta

Advocate Health is seeking a Clinical Research Coordinator in North Carolina to support AD genetics studies. You will recruit participants, conduct visits, obtain consent, collect samples, and administer cognitive tests.

You will coordinate with investigators, program managers, and site staff, travel to participant locations, and ensure study compliance, with flexibility for non-traditional hours as needed.

Qualificações

• Bachelor's degree in public health or a relevant clinical discipline; master's preferred.
• Experience in a medical or research setting; paramedical or clinical experience.
• At least one year of clinical or survey research experience including interviewing and supervision of data collection.
• Equivalents considered in education/experience.
• Phlebotomy license preferred.
• Registered Record Administrator preferred.
• Valid NC Driver's License.

Responsabilidades

• Recruit participants for Alzheimer’s disease genetics research and conduct participant visits.
• Obtain informed consent and collect blood samples.
• Administer cognitive assessments and collect family/medical histories.
• Prepare and ship research specimens; participate in IRB submissions and study documentation.
• Travel to participant locations and collaborating sites; may require non-traditional hours.
• Provide outreach/education about AD and related dementias.

Conhecimentos

Clinical research experience

Interviewing

Data collection supervision

Travel willingness

Formação académica

Bachelor's degree in public health or related field

Master's degree preferred

Ferramentas

SOCRA or ACRP Certification

CITI certification

Descrição da oferta de emprego

Advocate Health is seeking a Clinical Research Coordinator in North Carolina to support AD genetics studies. You will recruit participants, conduct visits, obtain consent, collect samples, and administer cognitive tests.

You will coordinate with investigators, program managers, and site staff, travel to participant locations, and ensure study compliance, with flexibility for non-traditional hours as needed.