Senior Clinical Research Associate - UK

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

At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post‑marketing.

Our therapeutic expertise spans renal, cardiometabolic, and oncology, areas where we make a significant impact on improving global health.

At the heart of our success is our ability to combine global reach with local knowledge. Our on‑the‑ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results, bringing therapies to patients in need.

About The Role

We are seeking an experienced Senior Clinical Research Associate (SCRA) to join our Clinical Operations team in the United Kingdom. In this role, you will be responsible for overseeing site management and monitoring activities across clinical trials, ensuring studies are conducted in accordance with protocols, ICH‑GCP, regulatory requirements, and company SOPs. As a Senior CRA, you will act as a key link between investigative sites and the project team, ensuring high standards of data quality, subject safety, and protocol compliance. This role requires strong independent monitoring experience, excellent communication skills, and the ability to build trusted relationships with investigators and site staff. You will work closely with cross‑functional teams to ensure studies are delivered on time and to the highest quality standards.

Your Responsibilities

• Conduct all monitoring visits in accordance with the study monitoring plan, including site selection visits, site initiation visits, routine monitoring visits, and close‑out visits
• Act as the primary contact for investigative sites, building strong professional relationships with site staff
• Ensure participant safety, protocol adherence, and data integrity throughout the study lifecycle
• Review source documentation and clinical trial data to ensure accuracy, completeness, and compliance
• Identify and escalation risks, issues, or protocol deviations in a timely manner
• Support sites with study start‑up activities and provide ongoing training and guidance where required
• Monitor site performance including recruitment, data quality, and study timelines
• Collaborate with project managers, clinical trial assistants, start‑up teams, and other cross‑functional stakeholders
• Prepare and maintain accurate monitoring documentation, including visit reports and follow‑up communications
• Support audit readiness and contribute to regulatory inspection preparation where necessary
• Provide guidance and mentorship to junior CRAs where appropriate

About You

• Previous experience as a Clinical Research Associate within a CRO, pharmaceutical, or biotechnology organisation
• Strong independent monitoring experience across all monitoring visit types
• Solid knowledge of ICH‑GCP, clinical trial regulations, and monitoring best practices
• Experience managing multiple investigative sites and maintaining strong site relationships
• Excellent organisational skills with the ability to manage competing priorities
• Strong communication and stakeholder management skills
• Comfortable working independently in a remote, field‑based environment
• Willingness to travel across the UK for site visits as required
• Full right to work in the United Kingdom

Why Join Us?

At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first, both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.

Here’s What Makes Us Stand Out

• Purpose‑Driven Work: You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
• Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.
• Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.

What We Offer

• Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.
• Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.
• Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
• Employee Wellbeing: Participate in programs and initiatives designed to promote work‑life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.
• Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.

We are an equal‑opportunity employer and encourage applications from all qualified candidates.

Interested? Apply now and help us achieve our mission to improve the health of millions worldwide.