Senior Clinical Research Associate – Site Engagement & Data Integrity

BioSpace; England; On-site; GBP 35,000 - 50,000; Full time

Job summary

AbbVie is advancing its clinical research pipeline by partnering with investigators to ensure high-quality trials and patient safety. The role focuses on site engagement, training, and monitoring to drive data integrity and study performance while maintaining strong collaborations with investigators and staff.

Ideal candidates have a health-related tertiary qualification and practical experience in clinical monitoring or similar roles, with familiarity of GCP, ICH guidelines, and regulatory

Qualifications

• Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing) preferred.
• Minimum of 1 year of clinically related experience, 6 months in clinical research monitoring.
• Advanced knowledge of local regulatory and ICH/GCP guidelines.

Responsibilities

• Serve as primary point of contact for investigative site and coordinate with site staff.
• Align and motivate site staff and PI on trial goals and patient treatment principles.
• Conduct site evaluations, trainings, and monitoring activities per protocol and GCP.

Skills

Cross-functional collaboration

Planning and organizational skills

Interpersonal skills

Communication skills

Critical thinking

Education

Health related degree

Tools

CRM tool

Job description

AbbVie is advancing its clinical research pipeline by partnering with investigators to ensure high-quality trials and patient safety. The role focuses on site engagement, training, and monitoring to drive data integrity and study performance while maintaining strong collaborations with investigators and staff.

Ideal candidates have a health-related tertiary qualification and practical experience in clinical monitoring or similar roles, with familiarity of GCP, ICH guidelines, and regulatory