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- Tasks: Design and analyse clinical trials for innovative RNA-editing medicines.
- Company: Join a pioneering biotechnology firm focused on transforming patient care.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real difference in patients' lives through groundbreaking research.
- Qualifications: Advanced degree in life sciences and 2-6 years of clinical experience.
- Other info: Collaborative environment with a focus on rare diseases and impactful projects.
The predicted salary is between 36000 - 60000 £ per year.
BioTalent are excited to partner with a biotechnology client developing RNA-editing medicines for patients with rare and common diseases in recruiting a clinical scientist for their team. This position will support the design, execution and analysis of clinical trials and work cross functionally to ensure scientific integrity and operational excellence in company sponsored trials.
Your responsibilities will include:
Clinical Trial Design & Protocol Development
- Assist in or lead the design of clinical study protocols and amendments
- Write or contribute to study-related documents (e.g., IB, informed consent forms, CRFs, recruitment materials)
Study Execution Support
- Provide scientific and clinical input during trial conduct
- Monitor data for consistency, completeness, and potential safety/efficacy signals
- Collaborate with CROs, sites, and internal teams to resolve study-related issues
- Build relationships with sites including PIs and clinical trial site staff, supporting their start up activities and patient recruitment activities
Data Analysis & Interpretation
- Review clinical trial data in collaboration with data management and biostatistics
- Interpret data in the context of the disease, target, and competitive landscape
- Contribute to clinical study reports and documentation for regulatory submissions
Cross-functional Collaboration
- Work closely with Clinical Operations, Medical Monitors, Pharmacovigilance, and Regulatory Affairs
- Participate in clinical development plan creation and updates
- Present study results and strategy to internal stakeholders and internal governance bodies
Regulatory & Safety Input
- Support preparation of INDs, NDAs, CTAs and other regulatory documents
- Provide input into safety review processes and risk-benefit assessments
Ideally, you will have:
- An advanced degree in life sciences or health discipline (PhD, Pharmacy degree, MD, or MS with relevant experience)
- 2–6+ years of industry experience in clinical development and/or clinical operations
- Strong knowledge of ICH GCP and clinical trial methodology
- Ability to critically evaluate scientific data and literature
- Strong communication skills (verbal and written)
- Ability to manage multiple priorities and collaborate across functions
- Experience in rare disease
- Familiarity with working with and supporting clinical trial sites for study start-up and recruitment
- Working knowledge of clinical trial site monitoring
- Ability to travel to clinical trial sites and build relationships with PIs and clinical trial site staff
LOCATION: This is a remote position that will require travel to sites. A candidate based in Europe/UK is preferred
Clinical Scientist employer: BioTalent
Contact Detail:
BioTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Scientist
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups related to clinical trials and biotechnology. Building relationships can open doors to opportunities that aren’t even advertised.
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your relevant experience and skills. Talk about specific projects you've worked on, especially those involving clinical trial design or data analysis, to show you’re the right fit for the role.
✨Follow Up After Interviews
Don’t just leave it at the interview! Send a quick thank-you email to express your appreciation for the opportunity and reiterate your interest in the position. It’s a simple way to keep yourself top of mind.
✨Apply Through Our Website
We’ve got a fantastic platform for job applications! Make sure to apply through our website to ensure your application gets the attention it deserves. Plus, you’ll find loads of resources to help you ace the process!
We think you need these skills to ace Clinical Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Scientist role. Highlight your relevant experience in clinical trial design and execution, and don’t forget to mention any specific skills that match the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about RNA-editing medicines and how your background makes you a perfect fit for our team. Keep it concise but impactful!
Showcase Your Communication Skills: Since strong communication is key for this role, make sure your written application reflects that. Use clear, professional language and structure your documents well to demonstrate your ability to convey complex information effectively.
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’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at BioTalent
✨Know Your Science
Make sure you brush up on the latest developments in RNA-editing and clinical trial methodologies. Being able to discuss recent advancements or challenges in the field will show your passion and expertise, which is crucial for a Clinical Scientist role.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific situations, like resolving issues with CROs or managing data inconsistencies. Think of examples from your past experience where you successfully navigated similar challenges, as this will demonstrate your problem-solving skills.
✨Showcase Your Collaboration Skills
Since this role involves working cross-functionally, be ready to discuss how you've effectively collaborated with different teams in previous positions. Highlight any experiences where you built relationships with clinical trial sites or contributed to team success.
✨Understand Regulatory Requirements
Familiarise yourself with the regulatory documents like INDs and NDAs that are relevant to the role. Being able to speak knowledgeably about these processes will not only impress your interviewers but also show that you're prepared for the responsibilities of the position.