Senior Clinical Research Associate, CFSP – Global Trials

IQVIA Inc

Livingston

On-site

GBP 45,000 - 65,000

Full time

7 days ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

IQVIA is seeking a Senior CRA to join our Clinical Functional Service Partnership team in the UK. Work across sponsors, performing site qualification, initiation, monitoring and close-out visits on relevant programs with a focus on quality and compliance.

You will build strong relationships with investigators, ensure patient safety and data integrity, and support study start-up activities while collaborating with cross-functional teams. Travel up to 40–60% is required.

Qualifications

  • University degree in Life Sciences or related field.
  • Minimum 4 years on-site monitoring in CRO/pharma.
  • Strong knowledge of GCP/ICH and regulations.
  • Experience in sponsor-dedicated or cfSP environment preferred.
  • Excellent communication and stakeholder management.

Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out visits.
  • Ensure patient safety, data integrity, and study quality.
  • Build relationships with investigators and site staff.
  • Monitor progress: regulatory docs, recruitment, data queries.
  • Collaborate with sites to optimize recruitment and timelines.
  • Maintain ISF/TMF and monitoring reports, follow-ups.
  • Identify and escalate study risks and issues promptly.
  • Mentor junior team members and support training.

Skills

GCP/ICH knowledge
Site monitoring
Communication skills
Travel willingness
Cross-functional teamwork
Independent work
Regulatory knowledge

Education

University degree in Life Sciences or related

Job description

IQVIA is seeking a Senior CRA to join our Clinical Functional Service Partnership team in the UK. Work across sponsors, performing site qualification, initiation, monitoring and close-out visits on relevant programs with a focus on quality and compliance.

You will build strong relationships with investigators, ensure patient safety and data integrity, and support study start-up activities while collaborating with cross-functional teams. Travel up to 40–60% is required.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Clinical Research Associate – CFSP Leader
Senior Clinical Research Associate – CFSP Leader

IQVIA • Livingston

On-site
GBP 40,000 - 60,000
Senior Clinical Research Associate – CFSP, Global Trials
Senior Clinical Research Associate – CFSP, Global Trials

IQVIA Inc • Reading

On-site
GBP 42,000 - 65,000
Senior CRA II - Global Trials & Travel
Senior CRA II - Global Trials & Travel

IQVIA • Manchester

On-site
GBP 40,000 - 60,000
Senior Clinical Research Associate – CFSP
Senior Clinical Research Associate – CFSP

IQVIA Inc • Bath

Remote
GBP 40,000 - 65,000
Senior Clinical Research Associate - Global Trials Travel
Senior Clinical Research Associate - Global Trials Travel

IQVIA • Bath

On-site
GBP 45,000 - 60,000
Senior CRA: Global Trials & Impact (Travel 40–60%)
Senior CRA: Global Trials & Impact (Travel 40–60%)

IQVIA • Bath

On-site
GBP 50,000 - 65,000
Senior CRA: Global Clinical Trials & Site Leadership
Senior CRA: Global Clinical Trials & Site Leadership

IQVIA Inc • Livingston

On-site
GBP 55,000 - 75,000
Senior CRA: Global Trials Monitoring & Site Leadership
Senior CRA: Global Trials Monitoring & Site Leadership

IQVIA Inc • Manchester

On-site
GBP 40,000 - 60,000
Senior CRA – Global Clinical Trials & Mentorship
Senior CRA – Global Clinical Trials & Mentorship

IQVIA Inc • England

On-site
GBP 42,000 - 65,000
Senior CRA, CFSP Specialist – Global Trials
Senior CRA, CFSP Specialist – Global Trials

IQVIA • Reading

On-site
GBP 55,000 - 85,000