At a Glance
- Tasks: Oversee monitoring activities for sponsor-led oncology trials and ensure regulatory compliance.
- Company: Join Parexel, a leader in clinical research with a focus on innovation.
- Benefits: Enjoy remote work flexibility, competitive salary, and opportunities for professional growth.
- Other info: Be part of a supportive environment that values your expertise and career development.
- Why this job: Make a real impact in oncology research while working with a dynamic team.
- Qualifications: 4+ years in CRO or Pharma with experience in oncology trials and RECIST criteria.
The predicted salary is between 45000 - 55000 £ per year.
Parexel is seeking a Senior Clinical Research Associate in the UK to oversee monitoring activities for sponsor-led trials.
The role emphasizes regulatory compliance, ICH-GCP guidelines, and ensuring study conduct aligns with the protocol, CMP/SMP, and data integrity.
You will manage site performance, conduct on-site or remote monitoring as allowed, and escalate issues to the project team.
Experience in oncology trials and RECIST criteria is essential, with at least 4 years in CRO or Pharma
#J-18808-Ljbffr
Senior Oncology CRA (UK) - Remote Monitoring Expert employer: Parexel
At Parexel FSP, we pride ourselves on being an exceptional employer, offering a dynamic and supportive work environment for our IRT Vendor Start-up Manager role. With a focus on employee growth and development, we provide comprehensive training and opportunities to collaborate with industry experts, all while enjoying the flexibility of a home-based position in the UK or Ireland. Our commitment to excellence and innovation ensures that you will be part of a team that values your contributions and fosters a culture of success.
