Senior CRA: Drive Site Monitoring & Study Quality

IQVIA

Reading

On-site

GBP 45,000 - 60,000

Full time

9 days ago
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Job summary

IQVIA UK is expanding its Site Management team and seeking two Senior CRAs to monitor sites and manage study data in line with protocol, regulations and sponsor requirements. You will perform visits, support recruitment plans, provide protocol training, and ensure TMF/ISF documentation is maintained.

The role requires monitoring experience, GCP/ICH knowledge, and strong communication. This is an on-site position in the UK, with emphasis on collaboration with study teams and sites to achieve

Qualifications

  • Bachelor's degree in scientific discipline or health care.
  • Good knowledge of, and skill in applying, regulatory requirements (GCP/ICH).
  • Requires at least 2 years of on-site monitoring experience.
  • Strong written and verbal English communication skills.
  • Proficient in MS Word, Excel and PowerPoint; comfortable with laptop, iPhone/iPad.

Responsibilities

  • Perform site monitoring visits (selection, initiation, monitoring and close-out) per SOP and GCP.
  • Collaborate with sites to drive and track subject recruitment plans.
  • Administer protocol training and maintain communication with sites to manage expectations.
  • Evaluate site quality and adherence to regulations; escalate issues as needed.
  • Track regulatory submissions, recruitment, CRF completion, data queries and resolution; support start-up phase.

Skills

Attention to detail
Communication skills
Time and financial management
Relationship building

Education

Bachelor's Degree in scientific discipline or health care

Tools

MS Word
MS Excel
PowerPoint
iPhone/iPad usage

Job description

IQVIA UK is expanding its Site Management team and seeking two Senior CRAs to monitor sites and manage study data in line with protocol, regulations and sponsor requirements. You will perform visits, support recruitment plans, provide protocol training, and ensure TMF/ISF documentation is maintained.

The role requires monitoring experience, GCP/ICH knowledge, and strong communication. This is an on-site position in the UK, with emphasis on collaboration with study teams and sites to achieve

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