Clinical Research Associate

CCS-Global; Coventry; On-site; GBP 32,000 - 45,000; Full time

Job summary

CCS-Global invites applications for Clinical Research Associates (CRA I & II) to join a UK-based FSP for an exclusive client. You will conduct site visits, collaborate with investigative sites, and ensure data integrity across oncology, immunology and rare disease trials.

Progression paths include advancing to Senior CRA, Lead CRA and Clinical Project Management, supported by industry-leading training and a comprehensive benefits package.

Qualifications

• A degree in Life Sciences or related field is required; Nursing/Pharmacy backgrounds encouraged.
• A minimum of 6–12 months of independent on-site monitoring experience within the UK (CRA I) or 12–18+ months (CRA II).
• Strong knowledge of UK regulatory requirements and a solutions-first mindset.
• Must hold a valid UK driving license with the ability to travel nationwide.

Responsibilities

• Perform all site visits (SQV, SIV, RMV, COV) per ICH-GCP.
• Build consultative relationships with investigative sites across the UK.
• Manage complex clinical data ensuring patient safety and data integrity.
• Collaborate with a global project team to meet enrollment timelines and quality milestones.

Skills

Regulatory knowledge (UK)

On-site monitoring

Problem solving

Travel readiness

Education

Life Sciences degree

Job description

Join the Future of Clinical Research | CRA I & II (FSP)

Are you ready to elevate your monitoring career within a team that actually values your growth? Due to significant project wins and a rapidly expanding global portfolio, we are looking for dedicated Clinical Research Associates (CRA I & II) to join our world-class Functional Service Provider (FSP) team in the UK for an exclusive client to CCS-Global.

Why This Role?

We know the market is starting to get busy, but here is why CCS Global's client stands out:

• Clear Path for Progression: If you perform, you progress, with defined tracks into Senior CRA, Lead CRA, and Clinical Project Management.
• Great Work Structure: Say goodbye to burnout. The FSP model is designed for focus, allowing you to work deeply within a specific sponsor's pipeline with manageable site loads and travel needs and no onsite minimum's
• Best-in-Class Training: Whether you are a CRA I looking to master complex protocols or a CRA II aiming for leadership, their continuous professional development programs are industry-leading.
• Industry-Leaning Benefits: From competitive car allowances, new home office setups, to comprehensive private healthcare and generous pension and bonus structures.

The Opportunity

As part of the UK FSP team, you will be at the forefront of innovative trials in therapeutic areas such as Oncology, Immunology, and Rare Disease.

Key Responsibilities:

• Perform all types of site visits (SQV, SIV, RMV, and COV) in accordance with ICH-GCP.
• Build strong, consultative relationships with investigative sites across the UK.
• Manage complex clinical data and ensure the highest standards of patient safety and data integrity.
• Collaborate with a global project team to meet enrollment timelines and quality milestones.

What We’re Looking For

• Experience: A minimum of 6-12 months of independent on-site monitoring experience within the UK (for CRA I) or 12 to 18 months+ (for CRA II).
• Education: A degree in Life Sciences or a related field (Nursing/Pharmacy backgrounds are highly encouraged).
• Skills: Strong knowledge of UK regulatory requirements and a "solutions-first" mindset.
• Mobility: A valid UK driving license and the flexibility to travel to sites nationwide.