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- Tasks: Join a dynamic team to ensure successful execution of clinical trials in oncology.
- Company: Innovative biotech organisation focused on cutting-edge therapies.
- Benefits: Freelance role with flexible hours and the chance to make a real impact.
- Why this job: Be at the forefront of clinical research and contribute to life-changing therapies.
- Qualifications: Bachelor's in Life Sciences and 2+ years in clinical research required.
- Other info: Opportunity for travel and collaboration with top professionals in the field.
The predicted salary is between 35000 - 45000 £ per year.
Apsida Life Science are currently partnered with an innovative clinical-stage biotech organisation dedicated to advancing cutting-edge therapies in oncology. As part of their continued growth, they are now seeking an In-House Clinical Research Associate (IHCRA) to join their Clinical Operations team. This is an excellent opportunity to play a key role in ensuring the successful execution of clinical trials, working cross-functionally with internal teams and external partners.
- Reviews critical factors for site selection with Medical Science staff and Clinical Trial Manager
- Act as a QC reviewer for key study documentation including protocols, informed consent forms, and study materials
- Attends CRO CRA meetings periodically to provide further support and training to CRAs, and to gain insight into study challenges at site level
- Recruitment support initiatives (such as direct to coordinator enrolment calls, newsletters, flyer preparation) in collaboration with clinical operations and clinical science
- Reviews protocol deviation trends and works with Clinical Trial Manager to communicate expected actions to the CRO
Qualifications:
- Bachelor's degree in Life Sciences
- Minimum 2+ years of experience in clinical research, including site monitoring experience
- Strong understanding of ICH-GCP guidelines and clinical trial regulations
- Experience in oncology clinical research is highly desirable
- Familiarity with clinical systems, databases, and project management tools
- Willingness to travel up to 25%
If you are interested in learning more, please reach out to Nicole Skinner at Apsida Life Science.
In-House Clinical Research Associate - Freelance - UK Biotech in Oxford employer: Apsida Life Science
Contact Detail:
Apsida Life Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land In-House Clinical Research Associate - Freelance - UK Biotech in Oxford
✨Tip Number 1
Network like a pro! Reach out to your connections in the biotech field, especially those who work in clinical research. A friendly chat can lead to insider info about job openings or even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP guidelines and oncology research. We recommend practising common interview questions with a friend to boost your confidence.
✨Tip Number 3
Showcase your experience! When you get the chance to speak with potential employers, highlight your site monitoring experience and any specific projects you've worked on that relate to their needs.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals to join our team in advancing clinical trials.
We think you need these skills to ace In-House Clinical Research Associate - Freelance - UK Biotech in Oxford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the In-House Clinical Research Associate role. Highlight your relevant experience in clinical research and any specific skills that match the job description, like your understanding of ICH-GCP guidelines.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about oncology and how your background makes you a perfect fit for the team. Keep it concise but impactful!
Showcase Your Experience: Don’t just list your previous roles; describe your achievements and how they relate to the responsibilities of this position. Mention any experience with site monitoring or working with CROs to stand out.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any updates!
How to prepare for a job interview at Apsida Life Science
✨Know Your Stuff
Make sure you brush up on your knowledge of ICH-GCP guidelines and clinical trial regulations. Being able to discuss these confidently will show that you’re not just familiar with the basics, but that you truly understand the intricacies of clinical research.
✨Showcase Your Experience
Prepare specific examples from your past roles that highlight your site monitoring experience and any challenges you've faced in oncology research. This will help demonstrate your problem-solving skills and how you can contribute to the team.
✨Ask Smart Questions
Come prepared with insightful questions about the company’s current projects or their approach to clinical trials. This shows your genuine interest in the role and helps you gauge if the company is the right fit for you.
✨Be Ready to Collaborate
Since the role involves working cross-functionally, be ready to discuss how you’ve successfully collaborated with different teams in the past. Highlighting your teamwork skills will reassure them that you can thrive in a collaborative environment.