RN/Clinical Research Coordinator Job at Centricity Research
Aventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. Centricity Research is committed to revolutionize research by creating outstanding clinical trial experiences to improve the health of the community today and tomorrow through clinical research.
Currently, our rapidly expanding team and site network is looking for a RN/Clinical Research Coordinator who can work for us on a full-time, permanent basis, supporting us either on-site, within Mesa, AZ.
Responsibilities will include but are not limited to:
- Assist administration/investigators with study feasibility and selection of studies.
- Act as a liaison between the research staff and the sponsors, drug companies, IRB, federal, and state officials and other regulatory agencies.
- Schedule, prepare, and conduct monitor visits and sponsor/Federal Drug Administration audits.
- Attend investigator’s meetings and site initiation visits with the sponsor to review and assess progress and conduct the study.
- Coordinate protocol specific training for study staff and communicate important study updates such as study start-up and protocol amendments with all appropriate staff.
- Meet or exceed enrollment goals and modify recruitment strategies as necessary; recruit and screen patients for specific studies.
- Execute Informed Consent Forms according to ICH and GCP guidelines.
- Perform assessments at study visits according to protocol. Document study visits in source according to ALCOA-CCC.
- Collect, process, and ship laboratory samples according to protocol.
- Enter source document data into respective EDC vendor system and respond to queries in a timely manner.
- Perform vitals, ECG, and other study assessments required by protocol.
- Record adverse events and serious adverse events per sponsor guidance. Maintain timely follow-up to determine resolution of adverse event.
- Monitor investigational product temperature logs and report temperature excursions.
- Document protocol deviations and report to the IRB if applicable.
- Maintain regulatory documents from study start up to study completion.
Requirements:
- RN licensed to work in AZ required.
- Experience in research preferred.
- Proficient with Microsoft Office Suite, specifically Excel, required.
Centricity Research is committed to meet the accessibility needs of persons with disabilities in a timely manner. These accommodations will be available upon request.
We thank all candidates for their applications, however, only those candidates selected for an interview will be contacted
Centricity Research values the health and well-being of our employees, clients and patients and as such we have instituted a COVID-19 Mandatory Vaccination policy for all employees. All candidates receiving job offers will be required to provide proof of vaccination
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