DeUnemployment currently lists 7 live Clinical Research Coordinator jobs in Phoenix, refreshed daily from public ATS and company career feeds. Most openings are onsite.
Top employers hiring for Clinical Research Coordinator roles: arizona.
How much do Clinical Research Coordinator jobs pay? Typical salary for a Clinical Research Coordinator runs roughly $46,000–$84,000/yr (model estimate; varies by location and experience).
There are currently 7 live Clinical Research Coordinator jobs listed on DeUnemployment. The index is refreshed daily, so this number changes as employers post and close roles.
Most current Clinical Research Coordinator postings are onsite — about 0% are remote-friendly. Use the search filters to find the remote ones.
Typical pay for a Clinical Research Coordinator currently runs roughly $46,000–$84,000/yr based on our salary model, which varies by location and experience.
Figures reflect DeUnemployment’s live index of public job postings, refreshed daily.
The Clinical Research Coordinator I will work at site to help ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GC
A will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To en
Job Summary: Under the general supervision of a physician and the clinical and clinical research team in an outpatient setting, the Clinical Research Coordinator I (CRC I) is responsible for executing study-related activ
Recruitment and Enrollment: Conduct study eligibility screening, recruitment, interviews and evaluation of potential study participants per IRB-approved study protocols. Obtain informed consent, collect and maintain subj
Recruitment and Enrollment: Conduct study eligibility screening, recruitment, interviews and evaluation of potential study participants per IRB-approved study protocols. Obtain informed consent, collect and maintain subj
Study Start Up: Participate in evaluation of new clinical research protocol requests to assess feasibility of proposed study resource allocation and clinical needs. Serve as the primary resource to investigators, sponsor
Duties and Responsibilities (Responsibilities necessary to accomplish job functions) Assists coordinators with patient visits including scheduling/tracking, data acquisition/data entry, procedures such as biopsies, admin