Job Description
Job Details
Job Location 05-00-APCR - Asheville, NC
Salary Range $30.00 - $38.00 Hourly
Description 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.
COMPENSATION INFORMATION - Actual compensation may vary depending on job-related knowledge, skills, and experience.
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.
Qualifications Education and Certifications - High school diploma required
- Active RN, LPN, CMA, or RMA license required
- CCRC certification preferred
Qualifications and Experience
- Minimum 2 years of experience as a clinical research coordinator
- Proficient in venipuncture, subcutaneous injections, and IV medication prep/administration
- Skilled in obtaining ECGs, spirometry, and vital signs
- Experience with electronic data capture (EDC) systems
- Familiar with use of handheld electronic subject diaries
- Efficient in using EMRs for data review and subject recruitment (AthenaFlow preferred)
- Familiarity with Clario spirometry/ECG and FeNO devices preferred
- Experience processing/shipping lab specimens
- Comfortable working with regulatory staff and clinical research associates
- Timely documentation and source data completion for PI review
- Knowledge of relevant conditions such as asthma, allergic rhinitis, chronic urticaria, and atopic dermatitis preferred
- Flexible schedule to meet protocol and subject needs; ability to attend off-site meetings
- Strong communication, organizational skills, and professional appearance
Job Tags
Hourly pay, Full time, Part time, Local area, Flexible hours,