Clinical Studies Coordinator I, Alzheimer's Disease Research Center

Wake Forest University Health Sciences

Unknown, , US
Base: $24.10 - $36.15; bonus/equity: not specified...
Onsite
Alzheimer's disease research center
Observational research studies
Clinical trials
The Clinical Studies Coordinator I position at Wake Forest University Health Sciences focuses on overseeing observational research studies and clinical trials related to Alzheimer's disease. Candidates should have a strong educational background and experience in medical or research settings, with an emphasis on working with older adults

Job Summary

  • This on-site role within the Alzheimer's Disease Research Center involves working across a range of observational research studies and clinical trials, requiring comfort with older adults, both with and without cognitive impairment, and their care partners.
  • Responsibilities include compilation and collection of data, recruitment of subjects, and general coordination of clinical studies, performing 3-5 study visits per day and up to 10 cognitive assessments per week.
  • Advocate Health offers a comprehensive suite of Total Rewards including competitive compensation, generous retirement offerings, and programs that invest in career development, alongside health and welfare benefits and paid time off.

Matching Summary

Match Score: 85

The Clinical Studies Coordinator I position at Wake Forest University Health Sciences focuses on overseeing observational research studies and clinical trials related to Alzheimer's disease. Candidates should have a strong educational background and experience in medical or research settings, with an emphasis on working with older adults.

Salary

Base: $24.10 - $36.15; Bonus/Equity: Not specified; Benefits: Yes

Skills & Requirements

Must-have

  • Alzheimer's Disease Research Center
  • observational research studies
  • clinical trials
  • working with older adults
  • cognitive assessments
  • data collection process
  • patient records maintenance

Nice-to-have

  • comfortable with cognitive impairment
  • care partner interaction
  • troubleshooting study problems
  • developing study materials
  • cooperating with stakeholders

Key Requirements

  • Bachelor's degree or equivalent experience
  • Experience in medical/research setting
  • Paramedical or clinical experience
  • Registered Record Administrator preferred

Work Rights

Not specified

Tailored Resume

Cover Letter