Location: Asheville, NC
Job Type: Full-Time
Reports To: Principal Investigator, Sub-Investigator
Job Summary
We are seeking an experienced and organized Clinical Research Coordinator to manage the clinical aspects of adult and/or pediatric research trials. Most studies are industry-sponsored and focus on respiratory and allergy-related conditions.
Key Responsibilities
Clinical Support
- Perform all research tasks per site-specific SOPs and study protocols
- Maintain required certifications (GCPs, IATA, medical license, etc.)
- Follow all applicable federal, state, and local clinical research regulations
- Assist PI, sub-investigators, and clinical staff as needed
- Manage time efficiently and meet deadlines across multiple studies
Compliance and Administration
- Ensure patient confidentiality and HIPAA compliance
- Complete all mandatory annual training (OSHA, HIPAA, fraud prevention, cybersecurity, etc.)
Work Environment and Physical Demands
- Full range of body motion, including manual/finger dexterity and eye-hand coordination
- Standing and walking required; occasional lifting (up to 30 lbs)
- Normal vision and hearing necessary
- Regular exposure to bodily fluids and clinical materials
- Frequent contact with communicable diseases, needles, and toxic substances
Supervisory Responsibilities
- This position does not have supervisory responsibilities.
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Why Join Us?
Join a dedicated clinical research team consisting of a full-time, hands-on PI, backup Sub-investigator, Regulatory Affairs Coordinator and both full- and part-time Clinical Research Coordinators who carefully orchestrate cutting-edge research studies. Our site is well-respected in industry circles and having direct access to the world’s largest database of patients with allergies and asthma positions us to enroll well for most trials with little need for outside advertising. We offer a supportive work environment where your attention to detail and clinical skills will directly impact the future of medicine.
