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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 innovation and impact.
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. We can’t stress enough how important it is to build relationships; you never know who might help you land that dream job.
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your relevant experience and skills. Be ready to discuss specific projects you've worked on, especially those involving clinical trial design or data analysis. We want to see your passion for the field shine through!
✨Follow Up After Interviews
After an interview, don’t just sit back and wait! Send a quick thank-you email to express your appreciation for the opportunity. This not only shows your enthusiasm but also keeps you fresh in their minds. We love candidates who take initiative!
✨Apply Through Our Website
If you’re eyeing a position with us, make sure to apply directly through our website. It’s the best way to ensure your application gets seen by the right people. Plus, we often have exclusive roles listed there that you won’t find anywhere else!
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 Clinical Trials
Make sure you brush up on the latest trends in clinical trial design and methodology. Familiarise yourself with ICH GCP guidelines and be ready to discuss how they apply to your past experiences. This will show that you’re not just knowledgeable but also passionate about the field.
✨Prepare for Scenario Questions
Expect questions that ask you to solve hypothetical problems related to clinical trials. Think about challenges you've faced in previous roles and how you overcame them. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly.
✨Showcase Your Collaboration Skills
Since this role involves working cross-functionally, be prepared to share examples of how you've successfully collaborated with different teams. Highlight any experience you have with CROs or clinical trial sites, as this will demonstrate your ability to build relationships and resolve issues effectively.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your interest in the company and the role. Inquire about their current projects in RNA-editing medicines or how they approach patient recruitment for clinical trials. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.