At a Glance
- Tasks: Monitor and deliver exciting oncology clinical trials across the UK.
- Company: Join a leading organisation in clinical research with a global impact.
- Benefits: Competitive salary, travel opportunities, and professional development.
- Other info: Flexible travel and excellent career growth potential.
- Why this job: Make a difference in cancer research while working in a dynamic environment.
- Qualifications: 5+ years as a CRA with oncology trial experience required.
The predicted salary is between 36000 - 60000 £ per year.
We are seeking an experienced Senior Clinical Research Associate (SCRA) to support the monitoring and delivery of Phase I-III oncology clinical trials across the UK. This role is ideal for a proactive, highly organized CRA with strong oncology experience who thrives in a fast‑paced, international research environment. You will be responsible for overseeing multiple clinical trial sites, ensuring compliance with regulatory requirements, and maintaining high standards of data quality and patient safety.
Key Responsibilities
- Conduct on‑site and remote monitoring visits for Phase I-III oncology clinical trials
- Oversee site performance, data quality, and protocol compliance
- Apply and assess RECIST criteria confidently within oncology studies
- Ensure compliance with ICH‑GCP, regulatory requirements, and study protocols
- Identify, anticipate, and elevate study‑related issues, developing effective solutions
- Build strong relationships with investigators, site staff, and internal stakeholders
- Prepare accurate and timely monitoring reports and documentation
- Support early‑phase oncology studies where required
Education & Experience
- Bachelor's degree (BSc, BA, RN, or equivalent) in a biological or science‑related field, or equivalent experience
- Minimum of 5 years' experience as a Clinical Research Associate
- Proven track record of on‑site monitoring in oncology trials
- Experience monitoring Phase I-III oncology studies (early phase experience required)
Skills & Competencies
- Strong working knowledge of ICH‑GCP and regulatory requirements
- Excellent multitasking, execution, and problem‑solving skills
- High level of organizational ability, efficiency, and attention to detail
- Outstanding interpersonal, communication, and presentation skills
- Ability to work collaboratively within a team environment
- Strong written and verbal communication skills
- Proficient in Microsoft Outlook, Word, and Excel
Additional Requirements
- Fluent in English and Spanish
- Willingness and ability to travel domestically and internationally as required (approximately 6-7 days per month)
- Ability to commute within 1 hour of a major airport or railway station
- Valid driver's license and passport preferred
- Successful completion of background clearance checks
Study & Site Details
- Number of studies: approximately 1-3
- Number of sites: 4-7
- Site locations include: Manchester, London, Glasgow, Liverpool, Sheffield, and Cardiff
Candidate Profile (Essential Criteria)
- At least 5 years of oncology CRA on‑site monitoring experience
- Confident application of RECIST criteria
- Experience monitoring Phase I-III oncology trials
- Based in the UK with strong travel flexibility
Senior CRA in Crawley employer: SEC Recruitment Ltd
Join a leading organisation that prioritises employee development and fosters a collaborative work culture, making it an exceptional employer for Senior Clinical Research Associates. With a focus on oncology clinical trials across the UK, you will benefit from a dynamic environment that encourages professional growth, offers competitive remuneration, and provides opportunities to work with cutting-edge research while building strong relationships within the healthcare community.
StudySmarter Expert Advice🤫
We think this is how you could land Senior CRA in Crawley
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We think you need these skills to ace Senior CRA in Crawley
Some tips for your application 🫡
Show Off Your Lab Skills:In the biotechnology field, it's super important to highlight your lab experience in your CV. Be sure to mention specific techniques or instruments you've mastered (think PCR, gel electrophoresis, etc.) and any relevant projects you've worked on. This will show SEC Recruitment Ltd that you have the hands-on skills they need.
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How to prepare for a job interview at SEC Recruitment Ltd
✨Brush Up on Lab Techniques
Since you're eyeing a full-time gig in biotechnology, make sure you're well-versed in the lab techniques relevant to the role. Be ready to talk about PCR, CRISPR, or any specific methods mentioned in the job description at SEC Recruitment Ltd. You might even be asked to demonstrate your understanding of these processes.
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Get comfortable with bioinformatics tools that are commonly used in the industry, like BLAST or Bioconductor. These are key in biotechnology, and having hands-on experience or at least familiarity can set you apart. Prepare to discuss any relevant projects you've worked on, especially if they involved data analysis or genomic research.
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