Highlights :
- $55,000 - $75,000 salary + Excellent Benefits
- Full Benefits and Consistent M-F schedule
- Fast growing company with tons of opportunity!
This is an on-site position, M-F, in the Matthews area of Charlotte, NC. Please do not apply if you are seeking Hybrid or Remote
The Company :
Our client is a clinical research site network organization that has a proven track record of success in clinical research.
They have partnership with a vast network of community based physicians and they make it easier for diverse patient populations to participate in clinical trials and by consistently delivering reliable results & quality data.
They are fast growing, constantly partnering and acquiring new sites and organizations. They are on track to become one of the largest site networks in the country!
The Role :
You will be responsible for daily, patient-facing responsibilities / clinical support, reporting, and back-office support for assigned studies.
The most successful candidate for this opportunity will have experience in all facets of a research study. Start-up to close-out, phase I - IV, (phlebotomy experience not necessary, but a PLUS!) and able to handle multiple studies at a time.
- Conducts assigned studies (2 - 5 at a time generally) according to protocol & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines
- Scheduling and screening of patients for study enrollment, consents, follow-ups
- Patient recruitment as needed
- Documenting charts entering data in EDC and answering queries
- Obtaining vital signs, ECGs, and lab procedures
- Maintaining & ordering study specific supplies
- Conducting monitoring visits, Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs)
- Filing SAE / Deviation reports to Sponsor and IRB; Handles all IRB functions
- Documenting and reporting adverse events
- Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF
Requirements :
- 2+ years experience as a Clinical Research Coordinator
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