Senior Clinical Research Associate (Senior CRA)

JR United Kingdom; Slough; Hybrid; GBP 40,000 - 55,000; Full time

Job summary

A leading global specialty pharmaceutical company is seeking a Senior Clinical Research Associate to enhance their dynamic team in Slough. This role focuses on site monitoring and ensuring compliance with regulatory requirements. Candidates should have 4-5 years of CRA experience and possess strong communication and problem-solving skills, with the flexibility to operate across various therapeutic areas.

Benefits

Competitive Compensation Package

Flexible Hybrid Working Model

Supportive Environment with Diverse Clinical Projects

Qualifications

• 4-5 years of experience as a Clinical Research Associate.
• On-site monitoring experience is essential.
• Proven ability to work independently with minimal oversight.

Responsibilities

• Conduct on-site monitoring visits including initiation, routine, and close-out visits.
• Ensure trials are conducted according to protocol, SOPs, ICH-GCP.
• Build and maintain strong site relationships.

Skills

Site Monitoring

Communication

Problem-Solving

Job description

Social network you want to login/join with:

Senior Clinical Research Associate (Senior CRA), slough

col-narrow-left

Client:

EPM Scientific

Location:

slough, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

3

Posted:

31.05.2025

Expiry Date:

15.07.2025

col-wide

Job Description:

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 experienced Senior Clinical Research Associate (Snr CRA) to join a dynamic team based in West London. This role requires a strong background in site monitoring, with regular on-site presence (2 days/week). The ideal candidate will bring a minimum of 4-5 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!