Clinical Research Associate

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

Overview

As a Clinical Research Associate in Abbott Diabetes Care, you contribute to advancing diabetes care through clinical studies supporting innovative medical technologies. You’ll join a collaborative Clinical Affairs team in Witney, receiving mentoring and hands-on experience to build a career in clinical research monitoring. You’ll work with investigators and sites to ensure studies meet GCP, SOPs, and regulatory requirements, while developing your monitoring expertise. This role offers growth opportunities in a global healthcare leader focused on life-changing diabetes technologies.

Pay / Benefits

  • training and development opportunities
  • collaborative team environment
  • global healthcare leader
  • opportunity to work on life-changing technologies

Responsibilities

  • Support delivery of clinical studies ensuring conduct, documentation, and reporting align with study protocols, GCP, SOPs, and regulations
  • Develop and maintain relationships with clinical investigators, study sites, and research institutions
  • Assist with study start-up activities, ongoing monitoring, and overall study management
  • Review study documents, prepare reports and study materials, and aid safety information collection in collaboration with investigators
  • Collaborate with cross-functional teams to maintain high-quality study conduct and support patient recruitment/retention
  • Participate in site training to ensure clear understanding of protocol requirements and procedures
  • Continue to develop clinical research and monitoring expertise through structured development opportunities

Key requirements

  • Enthusiastic and motivated with an interest in healthcare innovation
  • Potential background: recent Life Sciences graduate, Clinical Trial Assistant, Research Nurse, Study Coordinator, or similar experience
  • Excellent communication
  • Organisational skills
  • Attention to detail
  • Good understanding of GCP and regulatory requirements
  • Familiarity with SOPs and study documentation
  • Basic clinical study monitoring concepts

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Posted: October 10th, 2026