Clinical Research Associate I — Site Monitor & Study Advocate

AbbVie; Maidenhead; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading pharmaceuticals company in the UK is looking for a Clinical Research Monitor to ensure protocol adherence and quality data submission. The role involves site qualification, initiation, and closeout visits for clinical studies. The ideal candidate will possess a tertiary qualification in a health-related field and have experience in clinical research monitoring. Strong analytical and organizational skills are essential for success in this dynamic environment.

Qualifications

• Experience in on-site monitoring of drug or device trials.
• Strong understanding of therapeutic indications related to clinical trials.
• Knowledge of regulations governing clinical research and ICH/GCP Guidelines.

Responsibilities

• Monitor clinical investigative sites for protocol adherence.
• Conduct site qualification, initiation, and closeout visits.
• Manage investigator payments and negotiate contracts.

Skills

Clinical research monitoring

Planning and organizational skills

Analytical and conceptual capabilities

Interpersonal skills

Education

Tertiary qualification in health related field

Job description

A leading pharmaceuticals company in the UK is looking for a Clinical Research Monitor to ensure protocol adherence and quality data submission. The role involves site qualification, initiation, and closeout visits for clinical studies. The ideal candidate will possess a tertiary qualification in a health-related field and have experience in clinical research monitoring. Strong analytical and organizational skills are essential for success in this dynamic environment.