Senior Clinical Research Associate (Senior CRA)

About Us:

We are a global specialty pharmaceutical company dedicated to improving the lives of patients through the development of innovative and targeted therapies. Our focus is on addressing unmet medical needs, particularly in rare and underserved conditions. We offer a collaborative and dynamic work environment where clinical research professionals are empowered to contribute meaningfully.

About the Role:

We are seeking an experiencedSenior Clinical Research Associate (Snr CRA)to join a dynamic team based inWest London. This role requires a strong background insite monitoring, with regular on-site presence (2 days/week). The ideal candidate will bring a minimum of4-5 years of CRA experience, with a solid understanding of clinical trial processes and regulatory requirements.

Key Responsibilities:

• Conduct on-site monitoring visits, including initiation, routine, and close-out visits.
• Ensure trials are conducted, recorded, and reported in accordance with the protocol, SOPs, ICH-GCP, and applicable regulatory requirements.
• Build and maintain strong site relationships.
• Identify and resolve issues at clinical sites to ensure data quality and compliance.
• Prepare monitoring visit reports and follow up on action items.
• Collaborate cross-functionally with project teams.
  

Requirements:

• 4-5 years of experience as a Clinical Research Associate.
• Must have been a site monitor-on-site monitoring experience is essential
• Proven ability to work independently with minimal oversight.
• Excellent communication and problem-solving skills.
• Flexibility across therapeutic areas (no specific experience required).
• Based within commutable distance to West London.
  

Why Join Us?

• Competitive compensation package.
• Flexible hybrid working model.
• Opportunity to work in a supportive and professional environment with diverse clinical projects.
  

To Apply:

If you are interested please submit your CV - look forward hearing from you!