CCS-Global

About the Company

CCS-Global were formed to offer dedicated clinical trial recruitment solutions on a Global basis.
With the demand on medication continuing to expand to meet the international requirements in many complex medical needs, CCS-Global are perfectly positioned to support clients hire the talent they need and active job seekers secure new opportunities, enabling the delivery of unique and life changing medications.

As a dedicated Life Sciences and Clinical Research partner, we cater to Global CRO's, Biotech & Pharmaceutical organisations, SME and Start-ups, we offer extensive experience within full life-cycle clinical development from Phase 1 first in human studies to post marketing, allowing us to deliver complete hiring solutions in Global Locations.

Listed Jobs

Company Name

CCS-Global

Job Title

Clinical Research Associate

Job Description

**Job Title** Clinical Research Associate **Role Summary** Execute and manage clinical trial site visits (Screening, Initial, Regular, and Closing) in accordance with ICH‑GCP. Build and maintain consultative relationships with investigators across the UK, ensuring protocol adherence, data integrity, and patient safety. Work collaboratively with global project teams to meet enrolment targets and quality milestones, while supporting the next‑generation of clinical research through dedicated monitoring and professional development. **Expectations** * Perform independent on‑site monitoring (6–12 months experience for CRA I, 12–18 months+ for CRA II). * Demonstrate a solutions‑first mindset with strong analytical and problem‑solving skills. * Progress through defined career tracks: Senior CRA → Lead CRA → Clinical Project Management. * Maintain a flexible schedule for nationwide site visits and travel as required. **Key Responsibilities** 1. Conduct all site visit types (SQV, SIV, RMV, COV) per ICH‑GCP and sponsor protocols. 2. Foster strong, consultative relationships with investigative sites. 3. Manage complex clinical data ensuring patient safety and data integrity. 4. Collaborate with global project teams to meet enrolment timelines and quality milestones. 5. Record and report monitoring findings, deviations, and corrective actions. **Required Skills** * Independent on‑site monitoring experience (UK setting). * Strong knowledge of UK regulatory requirements (MHRA, NICE, etc.). * Excellent written and verbal communication skills. * Solutions‑first mindset and proactive problem‑solving. * Valid UK driving licence and willingness to travel nationwide. **Required Education & Certifications** * Bachelor’s degree in Life Sciences or a related field (Nursing/Pharmacy backgrounds highly encouraged). * Familiarity with ICH‑GCP guidelines; additional GCP certification preferred.

United kingdom

Remote

09-03-2026