What are the responsibilities and job description for the clinical research coordinator consultant virtual study position at Edwards-Hunt Group?
Company Description
Edwards-Hunt Group (EHG) specializes in high-impact, real-world data solutions by integrating the patient perspective with rigorous clinical research. With extensive expertise in clinical operations, EHG collaborates with life sciences companies, diagnostics firms, clinical research networks, and financial entities such as hedge funds and private equity firms. The group is committed to delivering research that not only enhances patient outcomes but also provides valuable insights for investment and strategic decision-making.
We’re hiring: Clinical Research Coordinator Consultant – Virtual Rare Disease Study
EHG is seeking an experienced independent consultant to support a virtual rare genomic disorder study. This is a part-time 1099 consultant role, approximately 24 hours per week, with hours that may fluctuate based on patient volume and study needs.
We are looking for a coordinator with 2 years of clinical research coordinator experience, including virtual study experience, who genuinely enjoys engaging with patients and families. This role requires someone who is confident with informed consent discussions, strong in remote visit coordination, highly detail-oriented with EDC/CTMS entry, and able to work independently in a remote environment.
Key details:
- Remote, must be based in the Central Time Zone
- Preferred schedule: Monday, Tuesday, and Friday
- Some participant calls may extend through 7:00 PM CT
- Occasional weekend travel for recruitment events, including possible overnight travel
- Contract term through the end of 2026, with potential to extend
Required qualifications:
- 2 years of CRC experience
- Prior virtual clinical research experience
- Strong patient engagement and follow-up skills
- Experience with informed consent/eConsent
- Office 365 proficiency and light CTMS/EDC experience
- Human Research Protection, GCP, and HIPAA training
- Personal laptop and private/confidential workspace
Preferred:
- Healthcare professional background
- Active healthcare license or certification
- Experience with adult and pediatric populations
Important: This opportunity is for a direct individual 1099 consultant only. Please no staffing firms, recruiting agencies, or staff augmentation companies.
When applying, please include short answers to these prescreening questions:
- Do you have 2 years of direct Clinical Research Coordinator experience?
- Have you supported virtual clinical research studies?
- Are you comfortable with informed consent/eConsent discussions with participants and families?
- Are your HRPT, GCP, and HIPAA training current?
- Have you worked previously as an independent 1099 consultant?
- Are you available for approximately 24 hours/week, preferably Monday, Tuesday, and Friday, with occasional calls through 7:00 PM CT?
- Are you applying as an individual consultant for yourself, and not on behalf of a staffing, recruiting, or staff augmentation company?
If this sounds like a fit, please send your resume to admin@edwardshunt.com.