Clinical Studies Coordinator I, Alzheimer's Disease Research Center

Wake Forest University Health Sciences

Unknown, Unknown, US
Base: $24.10 - $36.15; bonus/equity: not specified...
**
Alzheimer's disease research center
Observational research studies
Clinical trials
** Wake Forest University Health Sciences is seeking a Clinical Studies Coordinator I for its Alzheimer's Disease Research Center. This full-time, on-site role involves coordinating observational research studies and clinical trials, particularly focused on older adults, and requires a bachelor's degree along with relevant experience in a medical or research setting. **

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.
  • Responsibilities include data compilation and collection, subject recruitment, and general coordination of clinical studies, with a focus on working with older adults and their care partners.
  • Advocate Health offers a comprehensive suite of Total Rewards including competitive compensation, generous retirement offerings, and programs that invest in career development.

Matching Summary

Match Score: 75

** Wake Forest University Health Sciences is seeking a Clinical Studies Coordinator I for its Alzheimer's Disease Research Center. This full-time, on-site role involves coordinating observational research studies and clinical trials, particularly focused on older adults, and requires a bachelor's degree along with relevant experience in a medical or research setting. **

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

  • troubleshooting study management
  • patient referral tracking
  • interpreting medical records
  • designing study materials
  • supervising personnel
  • developing data collection codes

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