At a Glance
- Tasks: Conduct site visits and manage clinical data for innovative trials.
- Company: Join a leading global team in clinical research with a focus on growth.
- Benefits: Competitive salary, car allowances, private healthcare, and generous pension plans.
- Other info: Work on groundbreaking trials in Oncology, Immunology, and Rare Diseases.
- Why this job: Elevate your career with clear progression paths and industry-leading training.
- Qualifications: Experience in clinical monitoring and a degree in Life Sciences or related fields.
The predicted salary is between 40500 - 49500 £ per year.
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?
- Clear Path for Progression: If you perform, you progress, with defined tracks into Senior CRA, Lead CRA, and Clinical Project Management.
- Great Work Structure: 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 minimums.
- Best-in-Class Training: Their continuous professional development programs are industry-leading.
- Industry-Leading 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.
How to Apply
This is an exclusive vacancy managed by CCS Global. You won’t find this specific growth opportunity anywhere else. Take the next step in your career today. Ready to talk? Submit your CV directly by email.
Clinical Research Associate in Guildford employer: CCS-Global
CCS Global is an exceptional employer, offering Clinical Research Associates the chance to work with a leading organisation dedicated to advancing clinical research and improving patient outcomes. With a strong emphasis on career development, comprehensive training, and broad therapeutic exposure, employees can expect a supportive work culture that prioritises quality and innovation in clinical trials across the UK. Join us to be part of a forward-thinking team that values your expertise and fosters meaningful growth opportunities.
