Clinical Research Associate

CCS-Global; Chesterfield; On-site; GBP 28,000 - 42,000; Full time

Job summary

CCS-Global is seeking Clinical Research Associates (CRA I & II) for its UK FSP team. You will monitor oncology, immunology, and rare disease trials, performing site visits and building relationships with investigative sites across the UK.

The role emphasizes growth, training, and progression to senior CRA and leadership positions. You will work within a structured FSP framework, traveling to sites nationwide and ensuring high standards of data integrity and patient safety while collaborating

Qualifications

• Knowledge of UK regulatory requirements and ICH-GCP standards is essential.
• Ability to think in a solutions-first way to resolve site challenges.
• Willingness to travel and monitor sites on-site across the UK.

Responsibilities

• Perform on-site monitoring visits (SIV/SQV/RMV/COV) in line with ICH-GCP.
• Build and maintain strong relationships with investigative sites across the UK.
• Manage site data integrity and patient safety through close collaboration with the project team.
• Support enrollment timelines and meet quality milestones within sponsor pipelines.

Skills

UK regulatory knowledge

Solutions-first mindset

On-site monitoring

Site relationship building

Education

Life Sciences degree / Nursing or Pharmacy background

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.