Clinical Research Associate

Company: Abbott
Apply for the Clinical Research Associate
Location: Witney
Job Description:

Overview

In this Clinical Research Associate role, you will support the delivery of clinical studies in the diabetes care space, ensuring studies are conducted and documented to high standards. You will work with investigators, sites, and cross‑functional teams to start up, monitor, and manage studies in alignment with GCP, SOPs, and regulatory requirements. You’ll develop relationships with stakeholders and contribute to training and site readiness to drive quality and patient outcomes. This role offers structured development and hands-on experience in a global healthcare leader shaping diabetes technologies. A strong fit combines curiosity, collaboration, and a passion for improving patient lives.

Pay / Benefits

  • training and development opportunities
  • collaborative and supportive team environment
  • opportunity to impact diabetes care

Responsibilities

  • Support delivery of clinical studies per protocols, GCP, SOPs, and regulatory requirements
  • Develop relationships with clinical investigators, study sites, and research institutions
  • Assist with study start-up, ongoing monitoring, and overall study management
  • Review study documentation and prepare reports and study materials
  • Support collection and review of safety information with investigators
  • Collaborate with cross-functional teams to maintain high-quality study conduct
  • Assist with patient recruitment and retention initiatives
  • Contribute to site training to ensure understanding of protocol requirements and procedures
  • Build clinical research and monitoring expertise through development opportunities

Key requirements

  • Enthusiastic and motivated with a passion for healthcare innovation
  • Excellent communication and organizational skills
  • Strong attention to detail and ability to build stakeholder relationships
  • Eager to learn and maintain high-quality standards
  • Experience supporting clinical studies (e.g., Clinical Trial Assistant, Research Nurse, Study Coordinator) is advantageous
  • Interest in pursuing a career in clinical research
  • excellent communication
  • organizational skills
  • attention to detail
  • Good Clinical Practice (GCP)
  • Standard Operating Procedures (SOPs)
  • regulatory knowledge for clinical studies

…

Posted: October 17th, 2026