Travel-Heavy Clinical Research Associate – Site Monitoring

Travel-Heavy Clinical Research Associate – Site Monitoring

Full-Time 37305 - 45595 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead site monitoring and ensure compliance for clinical research protocols.
  • Company: MSD Malaysia, a leader in clinical research with a global impact.
  • Benefits: Competitive salary, travel opportunities, and professional development.
  • Other info: Expect 65–75% travel, including international trips.
  • Why this job: Join a dynamic team and make a difference in clinical research.
  • Qualifications: Experience in clinical research and strong organisational skills.

The predicted salary is between 37305 - 45595 £ per year.

MSD Malaysia is seeking a Clinical Research Associate to lead performance and compliance for assigned protocols and sites in the North West England region.

The role requires 65–75% travel, including days abroad, and reports to the CRA Manager or CRD.

You will manage site activities, ensure ICH/GCP adherence, and develop new sites to expand our clinical research footprint.

Key responsibilities include monitoring, data integrity, regulatory documentation, and cross‑functional collaboration with

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Travel-Heavy Clinical Research Associate – Site Monitoring employer: MSD Malaysia

Merck & Co., Inc. is an exceptional employer, offering a dynamic work environment in Rahway, NJ, where innovation meets a commitment to animal health and well-being. Employees benefit from a culture that prioritises collaboration, professional growth, and a strong sense of purpose, all while working with cutting-edge systems like SAP to enhance operational efficiency. With opportunities for continuous improvement and a focus on ethical integrity, Merck fosters a rewarding atmosphere for those looking to make a meaningful impact in global healthcare.

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Contact Details:

MSD Malaysia Recruitment Team

We think you need these skills to ace Travel-Heavy Clinical Research Associate – Site Monitoring

Site Monitoring
Performance Management
Compliance Adherence
ICH/GCP Knowledge
Data Integrity
Regulatory Documentation
Cross-Functional Collaboration