Clinical Research Coordinator jobs in South Carolina

Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or its equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator gains or has attained full proficiency in a specific area of discipline. Works under moderate supervision. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2020 Salary.com)

S
Nurse-Cath Lab--Days
  • Sunbelt Staffing
  • Charleston, SC
  • Assesses and coordinates patient's discharge planning needs with members of the healthcare team ... Demonstrates clinical competence in assisting the physician in caring for patients in the ...
  • 2 days ago

S
Contract-Perm- Cath RN
  • Sunbelt Staffing
  • Charleston, SC
  • Assesses and coordinates patient's discharge planning needs with members of the healthcare team ... Demonstrates clinical competence in assisting the physician in caring for patients in the ...
  • 2 days ago

South Carolina (/ˌkærəˈlaɪnə/ (listen)) is a state in the Southeastern United States and the easternmost of the Deep South. It is bordered to the north by North Carolina, to the southeast by the Atlantic Ocean, and to the southwest by Georgia across the Savannah River. South Carolina became the eighth state to ratify the U.S. Constitution on May 23, 1788. South Carolina became the first state to vote in favor of secession from the Union on December 20, 1860. After the American Civil War, it was readmitted into the United States on June 25, 1868. South Carolina is the 40th most extensive and 23...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$50,919 to $68,665

Clinical Research Coordinator in Alameda, CA
Assist in the management of external vendors.
January 14, 2020
Maintains regular internal contact with relevant departments such as Regulatory Affairs, Drug Safety, and others as necessary.
January 06, 2020
Review sample, investigator-prepared and IRB-approved informed consents.
January 05, 2020