Clinical Research Associate I β€” Frontline Study Monitors

Clinical Research Associate I β€” Frontline Study Monitors

Full-Time 37000 - 45000 Β£ / year (est.) No working from home possible
PSI CRO

At a Glance

  • Tasks: Monitor clinical sites, manage data quality, and ensure compliance with regulations.
  • Company: Join PSI CRO, a leader in clinical research operations.
  • Benefits: Gain valuable experience, travel opportunities, and a supportive work environment.
  • Other info: Exciting career growth potential in a dynamic industry.
  • Why this job: Be at the forefront of clinical research and make a difference in healthcare.
  • Qualifications: Life sciences background and willingness to travel required.

The predicted salary is between 37000 - 45000 Β£ per year.

PSI CRO in the United Kingdom is seeking a Clinical Research Associate I to join the frontline of clinical research operations.

You will monitor sites, manage data quality and interact with investigators to ensure timelines and regulatory compliance.

The role involves study startup involvement, CRF review, site communications, and feasibility activities.

Travel and a life sciences background are required to contribute to high-quality studies.

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Clinical Research Associate I β€” Frontline Study Monitors employer: PSI CRO

As a Remote Director of Business Development at our company, you will join a supportive and innovative team that prioritises employee well-being and professional growth. With a strong emphasis on collaboration and a commitment to making a difference in medical science, we offer a dynamic work culture, competitive benefits, and opportunities for career advancement, all while working from the comfort of your own home in the UK.

PSI CRO

Contact Details:

PSI CRO Recruitment Team

We think you need these skills to ace Clinical Research Associate I β€” Frontline Study Monitors

Site Monitoring
Data Quality Management
Regulatory Compliance
Study Startup Involvement
CRF Review
Site Communications
Feasibility Activities