Job Overview
NDx Clinical Research is growing, and we're seeking an experienced Clinical Research Coordinator to join our team in Dayton, Ohio.
This is an exciting opportunity for an experienced CRC who enjoys independently managing clinical trials, working closely with patients and investigators, and helping grow one of the Midwest's emerging CNS clinical research programs. NDx's expanding portfolio includes Alzheimer's disease and memory disorders, Parkinson's disease, migraines and other neurological conditions, as well as depression, bipolar disorder, and additional psychiatry therapeutic areas.
Depending on qualifications, experience, and demonstrated level of independent study management, the position may be structured at the CRC II, CRC III, or Lead CRC level.
Responsibilities
- Independently coordinate multiple industry-sponsored clinical trials
- Manage participant screening, informed consent, enrollment, study visits, and follow-up
- Review protocol requirements and coordinate participant eligibility with investigators
- Maintain accurate source documentation and complete timely EDC data entry and query resolution
- Identify, document, and facilitate reporting of AEs, SAEs, protocol deviations, and other safety information
- Coordinate investigational product accountability and protocol-specific procedures
- Prepare for and support monitoring visits, audits, and sponsor/CRO interactions
- Serve as a primary liaison among investigators, sponsors/CROs, study participants, and the research team
- Collaborate with recruitment staff to support enrollment goals and address recruitment barriers
- Maintain study documentation in accordance with GCP, FDA, protocol, and regulatory requirements
- Train and mentor research staff as appropriate to position level
Required
- 2+ years of direct clinical research experience, including experience coordinating industry-sponsored clinical trials
- Demonstrated ability to independently manage clinical trials and multiple competing priorities
- Experience with participant screening, informed consent, study visits, source documentation, EDC, and AE/SAE documentation
- Working knowledge of ICH-GCP, FDA regulations, and human subject protection requirements
- Strong organizational, communication, and problem-solving skills
- Experience with CTMS, EDC, eSource/eRegulatory, or other clinical research technologies
- Bachelor's degree or equivalent combination of education and relevant experience
Preferred
- Experience in Alzheimer's disease, neurology, psychiatry, or other CNS clinical trials
- CCRC, CCRP, or similar clinical research certification
- Experience managing complex Phase II–IV clinical trials
- Experience training or mentoring junior CRCs and research staff
For candidates being considered at the Lead CRC level, RN licensure is strongly preferred, along with demonstrated experience mentoring CRCs and experience with quality assurance or clinical research quality improvement.
Why NDx Clinical Research?
At NDx Clinical Research, you'll join a rapidly growing CNS research program, work alongside experienced investigators, and contribute to an expanding portfolio of innovative Alzheimer's disease, neurology, and psychiatry clinical trials. This is an opportunity to have a meaningful role in both patient care and the continued development of the research program.
Benefits
- 401(k)
- Health insurance
- Dental insurance
- Vision insurance
- Paid time off
- Retirement plan
Work Location: In person – Dayton, Ohio
Starting pay: $27/hour and up dependent on experience level of CRC.
We are actively looking to fill this position within the next few weeks and, at this time, will not be extending interviews to candidates who are located out of state or who are unable to begin working locally within our anticipated hiring timeframe.
Pay: From $27.00 per hour
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Flexible schedule
- Health insurance
- Paid time off
- Retirement plan
Work Location: In person
