Clinical Research Associate I: Site Monitoring

AbbVie; Maidenhead; On-site; GBP 30,000 - 45,000; Full time

Job summary

A global biopharmaceutical company in Maidenhead is seeking a Clinical Research Monitor to oversee clinical investigative sites for trial compliance. The successful candidate will be responsible for ensuring adherence to protocols, managing site interactions, and training personnel. A health-related tertiary qualification and clinical research monitoring experience are required. Strong analytical and interpersonal skills are essential. This position offers opportunities for professional growth within a leading firm committed to innovation and patient care.

Qualifications

• Experience in on-site monitoring of investigational drug/device trials required.
• Current knowledge of clinical research regulations and ICH/GCP Guidelines.
• Strong planning, organizational, and analytical skills.

Responsibilities

• Monitor clinical investigative sites to ensure protocol execution.
• Conduct site qualification, initiation, and monitoring visits.
• Ensure compliance with regulatory standards and quality of data.

Skills

Clinical research monitoring

Regulatory compliance

Analytical skills

Interpersonal skills

Education

Tertiary qualification in health-related field

Job description

A global biopharmaceutical company in Maidenhead is seeking a Clinical Research Monitor to oversee clinical investigative sites for trial compliance. The successful candidate will be responsible for ensuring adherence to protocols, managing site interactions, and training personnel. A health-related tertiary qualification and clinical research monitoring experience are required. Strong analytical and interpersonal skills are essential. This position offers opportunities for professional growth within a leading firm committed to innovation and patient care.