What are the responsibilities and job description for the Clinical Research Coordinator position at Noctrix Health, Inc.?
Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Our team of medical device specialists, neuroscientists, and consumer electronics engineers is dedicated to delivering prescription-grade therapy with an outstanding user experience. We have pioneered the world's first drug-free wearable therapy, clinically proven to alleviate symptoms in adults with drug-resistant Restless Legs Syndrome (RLS). Be part of our mission to transform healthcare, improve lives, and drive meaningful change with Noctrix Health.
The Clinical Research Coordinator will support the clinical research program at Noctrix Health, based in the company headquarters in Pleasanton, CA. This is a full-time, on-site position. This individual will be responsible for leading the successful execution of on-site clinical studies and supporting decentralized clinical studies. This position reports to the Staff Clinical Research Scientist.
Responsibilities:
The Clinical Research Coordinator will support the clinical research program at Noctrix Health, based in the company headquarters in Pleasanton, CA. This is a full-time, on-site position. This individual will be responsible for leading the successful execution of on-site clinical studies and supporting decentralized clinical studies. This position reports to the Staff Clinical Research Scientist.
Responsibilities:
- Execute study procedures in accordance with the study protocols
- Document procedures with source documents and case report forms
- Develop source documents and data entry systems for new studies
- Develop and maintain study databases
- Train study participants to ensure adherence to study procedures
- Develop and maintain procedures for conducting decentralized clinical studies
- Maintain and set up instrumentation to collect sensor data
- Obtain consent from study participants according to protocol
- Provide feedback to research team to improve study procedures
- Interact directly with study participants in accordance with local regulations, the IRB approved protocol, ICH/E6 GCP and 21 CFR 812
- 2 years clinical research or human subjects research experience
- 1 years research experience involving medical devices
- Experience with both on-site and decentralized clinical trials preferred
- Bachelor's degree in a scientific, medical, or engineering field
- Strong verbal interpersonal communication skills and written documentation skills
- Experience collecting physiological data with medical instrumentation
- Good Clinical Practice (GCP) certification
- Demonstrated ability to work independently
- Demonstrated flexibility and ability to learn rapidly in a fast-paced environment
- Base Pay: $72,000 to $80,000 per year
Salary : $72,000 - $80,000
