CCS-Global
Clinical Research Associate
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Clinical Research Associate
Senior CRA or Lead CRA - England, Fully Home-Based
Are you an accomplished Clinical Research Associate seeking a stimulating and pivotal career move? Do you excel in a culture where quality site engagement is prioritised over rigid metrics, and where your well-being is a core value? This is your chance to join a clinical research organisation with a strong UK presence.
We are specifically looking for candidates based within these regions:
- South West
- London
- Midlands
- North West
The client, a distinguished global Contract Research Organisation (CRO), is recruiting for a high-calibre CRA II, Senior CRA, or Lead CRA to drive clinical trials in high-impact therapeutic areas within the UK. These include:
- Oncology
- Haematology-Oncology
- Rare and Orphan Diseases
- Cutting-edge specialities
You will play a crucial role in ensuring compliant and efficient operation of these studies across networks of clinical sites.
Why Consider This Opportunity?
This organisation stands out by prioritising people, quality, and professional growth:
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- Empowerment and Quality-First Monitoring: They focus on proactive collaboration and trusting expert judgement over rigid visit protocols—greater flexibility is valued.
- Structured Career Advancement: Opportunities for clear progression paths supported by training, mentorship, and development resources.
- Meaningful Contribution: You’ll help refine clinical processes and shape the organisational culture, fostering employee engagement and longevity.
Your Role as a CRA II / Senior / Lead CRA
Location: Fully home-based, regionally focused (South West, London, Midlands, North West) Responsibilities include:
- Managing and overseeing clinical monitoring processes from site set-up to final closure in compliance with approved protocols, Good Clinical Practice (GCP), and UK/European regulations.
- Building and maintaining strong professional relationships with research investigators and site personnel.
- Ensuring study documentation is accurate, up-to-date, and compliant.
- Supporting less experienced CRAs when in the Lead CRA role.
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Essential Candidate Profile
To excel in this role, you should possess:
- Substantial experience in independent clinical monitoring during clinical trials.
- Deep knowledge of Good Clinical Practice (GCP) and UK regulatory requirements.
- Exceptional interpersonal skills, organisational aptitude, and analytical problem-solving.
- A proactive, diligent, and detail-oriented work ethic.
- Prior experience in therapeutic areas such as Oncology, Haematology-Oncology, or Rare Diseases (preferable).
If you’re seeking an engaging, supportive workplace where your expertise is valued and your career growth is actively nurtured—this organisation is for you.
Location: Fully home-based (South West, London, Midlands, or North West) How to Apply: Submit your CV to r.kelly@completeclinicalsolutions.com.
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