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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 cutting-edge therapies.
- Benefits: Freelance role with flexible hours and impactful work in life sciences.
- Why this job: Make a real difference in patient outcomes while growing your career.
- 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 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. 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 Chelmsford, 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 Chelmsford, Essex
✨Tip Number 1
Network like a pro! Reach out to your connections in the biotech field, especially those who are already working in clinical research. A friendly chat can lead to insider info about job openings or even referrals.
✨Tip Number 2
Get your LinkedIn game on point! Make sure your profile is up-to-date and highlights your experience in clinical research. Join relevant groups and engage with posts to get noticed by recruiters.
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of ICH-GCP guidelines and oncology research. Practice common interview questions and have examples ready that showcase your skills and experiences.
✨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 over other candidates.
We think you need these skills to ace In-House Clinical Research Associate - Freelance - UK Biotech in Chelmsford, 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, especially any site monitoring or oncology-related work. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how you can contribute to our innovative team. Keep it concise but impactful – we love a good story!
Showcase Your Skills: Don’t forget to highlight your organisational skills and familiarity with ICH-GCP guidelines. Mention any experience with clinical systems or project management tools, as these are key for the role. We’re looking for someone who can juggle multiple priorities with ease!
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 important updates. Plus, it’s super easy!
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.