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- Tasks: Join a dynamic team to ensure successful execution of clinical trials in oncology.
- Company: Innovative biotech firm focused on advancing impactful therapies.
- Benefits: Freelance role with flexible hours and the chance to make a real difference.
- Why this job: Be part of groundbreaking research that improves patient outcomes globally.
- Qualifications: Bachelor's in Life Sciences and 2+ years in clinical research required.
- Other info: Opportunity for travel and collaboration with top industry professionals.
The predicted salary is between 40000 - 50000 £ per year.
Apsida Life Science are currently partnered with an innovative clinical-stage biotech organisation dedicated to advancing cutting-edge therapies in oncology. With a strong and growing clinical pipeline, the company is committed to delivering impactful treatments that improve patient outcomes globally. 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.
Responsibilities:
- Site Feasibility Process
- Reviews critical factors for site selection with Medical Science staff and Clinical Trial Manager
- Reviews site feasibility/qualification reports from CRO to ensure evidence-based site assessments
- 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
Requirements:
- 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
- Excellent organisational skills with the ability to manage multiple priorities
- Willingness to travel up to 25%
If you are interested in learning more, please reach out to Nicole Skinner at Apsida Life Science: +44 74413 41417.
Locations
In-House Clinical Research Associate - Freelance - UK Biotech in Basildon, Essex 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 Basildon, Essex
✨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 that could land you an interview.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP guidelines and oncology research. We recommend doing mock interviews with friends or using online platforms to practice common questions. Confidence is key!
✨Tip Number 3
Showcase your skills! Create a portfolio that highlights your experience in clinical trials, site monitoring, and any relevant projects. This can be a great conversation starter during interviews and helps you stand out from the crowd.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you an edge. Plus, it’s super easy to keep track of your applications!
We think you need these skills to ace In-House Clinical Research Associate - Freelance - UK Biotech in Basildon, Essex
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 great fit for the team. Keep it concise but impactful!
Showcase Your Organisational Skills: Since the role requires excellent organisational skills, consider including examples of how you've managed multiple priorities in past roles. This will show us that you can handle the demands of the position.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates during the process!
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 clinical 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 clinical pipeline and their approach to site feasibility. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
✨Be Organised
Since the role requires managing multiple priorities, showcase your organisational skills during the interview. You could mention tools or methods you use to stay on top of tasks, which will reassure them that you can handle the demands of the position.