Senior Clinical Trials Monitoring Lead

Alira Health Group; Greater London; Hybrid; GBP 40,000 - GBP 60,000; Full time

Job summary

A leading global biopharmaceutical company seeks a Senior Clinical Research Associate (Sr CRA) to conduct site monitoring for clinical trials. The role involves oversight, compliance assurance, and collaboration with clinical teams. Candidates should have a background in the pharmaceutical industry, strong communication skills, and the ability to manage multiple priorities. This position offers opportunities for professional development, global travel, and flexible work programs.

Benefits

Professional development

Global travel

Flexible work programs

Qualifications

• 3 years of experience in the pharmaceutical / biotechnology / CRO industry for US applicants.
• Minimum 2 years of clinical monitoring experience for EU applicants.
• Strong command of English and local language for communication.

Responsibilities

• Conduct site monitoring responsibilities for clinical trials.
• Provide oversight and leadership in the management of clinical trials.
• Develop study-specific Monitoring Plans and assist with ethics documents.

Skills

Clinical research

Communication skills

Problem-solving

Organizational skills

Leadership

Attention to detail

Education

Graduation in a scientific health field

Certified Monitor in compliance with local regulations (Italy)

Tools

Clinical trial management systems

Electronic data capture systems

Job description

A leading global biopharmaceutical company seeks a Senior Clinical Research Associate (Sr CRA) to conduct site monitoring for clinical trials. The role involves oversight, compliance assurance, and collaboration with clinical teams. Candidates should have a background in the pharmaceutical industry, strong communication skills, and the ability to manage multiple priorities. This position offers opportunities for professional development, global travel, and flexible work programs.