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- Tasks: Manage clinical trial sites and ensure compliance with protocols while driving data integrity.
- Company: Join a top-5 Pharma company focused on groundbreaking oncology treatments.
- Benefits: Enjoy remote work options, performance incentives, travel allowances, and private medical coverage.
- Why this job: Make a global impact in medicine while growing your career in a supportive, innovative culture.
- Qualifications: 2-4 years as a Clinical Research Associate with strong GCP knowledge and excellent communication skills.
- Other info: Flexible working options and opportunities for professional development and corporate retreats.
The predicted salary is between 36000 - 60000 £ per year.
Top-5 Pharma Hybrid CLINICAL RESEARCH ASSOCIATE – Accelerate Innovation & Shape the Future of Medicine.
Location: London, United Kingdom (Fully remote options available)
I\’m working on an exciting opportunity with a top-5 Pharma client with a focus on a groundbreaking new treatment in Oncology, this role brings significant opportunities for growth and leadership for driven professionals.
What makes this opportunity exceptional?
- Impactful Work: Contribute to the advancement of vital medicines, impacting patient outcomes globally.
- Career Growth: Dedicated investment in your professional development, including career progression, engaged line management, technical and therapeutic area training, and peer recognition.
- Supportive Culture: Be part of our \”Total Self\” culture, where diversity of thoughts, backgrounds, and perspectives are celebrated, fostering a sense of belonging and taking care of our people.
- Innovation at Your Fingertips: Leverage cutting-edge tools and processes to enhance your monitoring capabilities and contribute to the evolution of clinical trial execution.
Key responsibilities:
- Own and Oversee Clinical Trial Sites: Take responsibility for managing assigned study sites, ensuring the highest standards of quality, compliance, and patient safety from initiation through close-out.
- Become a Trusted Partner: Build strong, collaborative relationships with investigators, site staff, and other stakeholders, providing guidance and support to ensure smooth and successful study conduct.
- Drive Data Integrity: Conduct thorough on-site and remote monitoring visits, performing Source Document Verification (SDV) to verify the accuracy and completeness of data and ensuring strict adherence to protocols, according to ScienceDirect.com.
- Navigate the Regulatory Landscape: Ensure meticulous compliance with Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements (e.g., FDA, EMA, MHRA).
- Empower Innovation: Actively participate in the design, implementation, and improvement of monitoring tools, procedures, and processes, such as developing monitoring plans, SOPs, and training materials.
Requirements:
- Proven CRA Expertise: Minimum of 2-4 years of experience as a Clinical Research Associate, demonstrating a strong understanding of clinical trial processes and a track record of successful site monitoring.
- GCP Mastery: In-depth knowledge and practical application of ICH-GCP guidelines and relevant regulatory requirements.
- Exceptional Communication & Interpersonal Skills: Ability to build rapport, communicate effectively with diverse stakeholders, and resolve issues collaboratively.
- Autonomous & Detail-Oriented: Ability to work independently, manage multiple priorities, and maintain meticulous attention to detail in all aspects of trial oversight.
- Tech-Savvy: Proficiency in using clinical trial management systems (CTMS) and other relevant software for efficient monitoring and data handling.
- Continuous Improvement Mindset: A proactive approach to identifying opportunities for process enhancement and contributing to a culture of excellence
Tangible benefits:
- Higher band negotiable salary & Performance-Based Incentives
- Travel Allowances & Expenses: Covering per diem and travel costs for UK and EU monitoring activities.
- Private medical.
- Professional Development & Career Growth: Opportunities for training, certifications, conference attendance, and advancement to senior roles.
- Flexible Working Options
- Corporate retreats
Hybrid Clinical Research Associate employer: Barrington James
Contact Detail:
Barrington James Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Hybrid Clinical Research Associate
✨Tip Number 1
Network with professionals in the clinical research field, especially those who have experience as Clinical Research Associates. Attend industry events or webinars to connect with potential colleagues and learn about the latest trends in oncology research.
✨Tip Number 2
Familiarise yourself with the specific regulatory requirements and guidelines relevant to the role, such as ICH-GCP. This knowledge will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Showcase your tech-savviness by getting hands-on experience with clinical trial management systems (CTMS). Familiarity with these tools can set you apart from other candidates and highlight your ability to adapt to innovative processes.
✨Tip Number 4
Prepare to discuss your previous experiences in managing clinical trial sites and how you ensured data integrity. Use specific examples to illustrate your problem-solving skills and ability to build strong relationships with stakeholders.
We think you need these skills to ace Hybrid Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate. Focus on your expertise in clinical trial processes, GCP knowledge, and any specific achievements that demonstrate your ability to manage study sites effectively.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for oncology and your commitment to advancing patient outcomes. Mention how your skills align with the company's values, particularly their focus on innovation and supportive culture.
Highlight Relevant Skills: In your application, emphasise your exceptional communication and interpersonal skills. Provide examples of how you've built strong relationships with stakeholders and resolved issues collaboratively in previous roles.
Showcase Continuous Improvement: Demonstrate your proactive approach to process enhancement by including examples of how you've contributed to improving monitoring tools or procedures in past positions. This will show your alignment with the company's emphasis on innovation.
How to prepare for a job interview at Barrington James
✨Showcase Your CRA Experience
Be prepared to discuss your previous roles as a Clinical Research Associate in detail. Highlight specific projects you've worked on, the challenges you faced, and how you overcame them. This will demonstrate your expertise and understanding of clinical trial processes.
✨Emphasise Communication Skills
Since building relationships with investigators and site staff is crucial, be ready to provide examples of how you've effectively communicated and collaborated with diverse stakeholders in past roles. This will show that you can navigate the interpersonal aspects of the job.
✨Demonstrate Regulatory Knowledge
Familiarise yourself with Good Clinical Practice (GCP) guidelines and relevant regulatory requirements. Be prepared to discuss how you've ensured compliance in your previous work, as this is a key responsibility of the role.
✨Highlight Your Tech Savviness
As the role requires proficiency in clinical trial management systems, mention any relevant software or tools you've used in your previous positions. Discuss how these technologies have improved your monitoring capabilities and contributed to successful trial execution.
