Senior Clinical Research Associate - Uk - Remote

Worldwide Clinical Trials

United Kingdom
2+ years cra experience
Site qualification and initiation visits
Source document verification
The role involves responsible site qualification, initiation, interim monitoring, and study close-out visits to ensure patient safety and data integrity

Job Summary

  • The role involves responsible site qualification, initiation, interim monitoring, and study close-out visits to ensure patient safety and data integrity.
  • Candidates will mentor less experienced CRAs and provide training to site staff on protocol adherence within a supportive global team.
  • Worldwide Clinical Trials is a midsize CRO committed to pioneering approaches and cultivating a diverse, inclusive environment for professionals.

Matching Summary

The role involves responsible site qualification, initiation, interim monitoring, and study close-out visits to ensure patient safety and data integrity.

Skills & Requirements

Must-have

  • 2+ years CRA experience
  • Site qualification and initiation visits
  • Source document verification
  • Protocol adherence training
  • Trial Master File management

Nice-to-have

  • Mentoring less experienced CRAs
  • Experience in CNS or Oncology
  • Collaborative team environment
  • Innovative problem solving
  • Diverse therapeutic area exposure

Key Requirements

  • 4-year university degree or RN/BSN
  • 2+ years as Clinical Research Associate
  • Willingness to travel required
  • Proficiency in CTMS and EDC Systems

Work Rights

Not specified

Tailored Resume

Cover Letter