Find & Apply For Clinical Research Coordinator Jobs In Jefferson, Alabama
Clinical Research Coordinator jobs in Jefferson, Alabama involve coordinating and overseeing research studies, ensuring compliance with protocols and regulations, recruiting participants, collecting data, and managing study budgets. Responsibilities also include preparing reports, collaborating with research teams, and maintaining accurate documentation. Below you can find different Clinical Research Coordinator positions in Jefferson, Alabama.
Jobs in Jefferson
Browse jobs from a variety of sources below, sorted with the most recently published, nearest to the top. Click the title to view more information and apply online.
Clinical Research Coordinator II – T225755
University of Alabama at Birmingham
Jefferson, AL
Faculty position in Nephrology
University of Alabama at Birmingham
Jefferson, AL
Clinical Research Coordinator I – T222719
University of Alabama at Birmingham
Jefferson, AL
HSOM-Open Rank-Medicine (Nephrology)
University of Alabama at Birmingham
Jefferson, AL
Part time Nurse Practitioner or Physician Assistant – (Fridays 8-4)
Alcanza Clinical Research
Jefferson, AL
Latest Jobs in Jefferson
Salary Information & Job Trends In this Region
Clinical Research Coordinators in Jefferson, Alabama, play a pivotal role in the management of clinical trials and research projects. - Entry-level Clinical Research Assistant salaries range from $38,000 to $48,000 per year - Mid-career Clinical Research Coordinator salaries range from $50,000 to $65,000 per year - Senior Clinical Research Manager salaries range from $70,000 to $90,000 per year The role of Clinical Research Coordinator in Jefferson has its roots in the broader medical research field, which has been developing over decades to improve health outcomes through systematic clinical studies. Over the years, the position of Clinical Research Coordinator in Jefferson has evolved from simple data collection roles to complex management positions overseeing entire clinical trials, ensuring compliance with regulatory standards, and maintaining ethical conduct throughout the study process. Current trends in the field include the increasing use of digital tools for data management, a greater focus on patient-centric practices in clinical trials, and an emphasis on interdisciplinary collaboration to optimize research efficacy and safety.
