Senior Clinical Research Associate - Remote/Hybrid UK Trials

Emerald Clinical; Staines-upon-Thames; Hybrid; GBP 40,000 - 60,000; Full time

Benefits offered by this job

Competitive compensation

Flexibility in working arrangements

Career growth opportunities

Employee wellbeing programs

Global opportunities for diverse projects

Job summary

A global Contract Research Organization is seeking an experienced Senior Clinical Research Associate to oversee site management and monitoring activities in the UK. This role requires expertise in ICH-GCP and strong communication skills to ensure data integrity, participant safety, and protocol compliance throughout clinical trials. The ideal candidate will have independent monitoring experience and the ability to maintain strong relationships with investigative sites. Join our team to help improve global health outcomes through impactful clinical research.

Qualifications

• Previous experience as a Clinical Research Associate within a CRO or pharmaceutical organisation.
• Strong independent monitoring experience across all visit types.
• Solid knowledge of ICH‑GCP and clinical trial regulations.
• Experience managing multiple investigative sites and maintaining site relationships.

Responsibilities

• Conduct monitoring visits in accordance with the study monitoring plan.
• Act as the primary contact for investigative sites.
• Ensure participant safety, protocol adherence, and data integrity.
• Support sites with study start‑up activities and provide ongoing training.

Skills

Independent monitoring experience

Excellent communication skills

Organisational skills

Stakeholder management

Job description

A global Contract Research Organization is seeking an experienced Senior Clinical Research Associate to oversee site management and monitoring activities in the UK. This role requires expertise in ICH-GCP and strong communication skills to ensure data integrity, participant safety, and protocol compliance throughout clinical trials. The ideal candidate will have independent monitoring experience and the ability to maintain strong relationships with investigative sites. Join our team to help improve global health outcomes through impactful clinical research.