Clinical Research Associate II – Site Monitoring Expert

AbbVie; Maidenhead; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading biopharmaceutical company in Maidenhead is seeking a Clinical Research Associate. The role involves monitoring clinical trials for adherence to protocols and regulations, managing site personnel, and ensuring data quality and participant safety. Candidates should have a health-related tertiary qualification and extensive experience in Oncology. Strong organizational and communication skills are essential, along with a thorough understanding of ICH/GCP guidelines. This position offers a dynamic work environment with a commitment to innovation and ethical standards.

Qualifications

• Extensive clinically-related experience in Oncology preferred.
• Current in-depth knowledge of regulations governing clinical research.
• Demonstrated business ethics and integrity.

Responsibilities

• Monitor activities of clinical investigative sites.
• Conduct site qualification and monitoring visits for studies.
• Oversee site personnel to meet study objectives.
• Ensure safety and protection of study subjects.
• Train site personnel on protocol and regulatory requirements.

Skills

Strong planning and organizational skills

Analytical and conceptual capabilities

Interpersonal skills

Communication skills

Knowledge of ICH/GCP Guidelines

Education

Tertiary qualification in a health-related field

Job description

A leading biopharmaceutical company in Maidenhead is seeking a Clinical Research Associate. The role involves monitoring clinical trials for adherence to protocols and regulations, managing site personnel, and ensuring data quality and participant safety. Candidates should have a health-related tertiary qualification and extensive experience in Oncology. Strong organizational and communication skills are essential, along with a thorough understanding of ICH/GCP guidelines. This position offers a dynamic work environment with a commitment to innovation and ethical standards.