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- Tasks: Join a dynamic team to provide statistical expertise in clinical trials.
- Company: Collaborate with a leading pharmaceutical company focused on impactful clinical development.
- Benefits: Enjoy flexible freelance work with opportunities for professional growth.
- Why this job: Make a real difference in healthcare while working in a science-driven environment.
- Qualifications: MSc or PhD in Biostatistics; experience in pharma or CRO settings required.
- Other info: Must be UK-based and eligible to work as a contractor.
The predicted salary is between 48000 - 72000 £ per year.
We’re working with a pharmaceutical company seeking an experienced Biostatistician to join their team on a contract basis. This is a fantastic opportunity to contribute to impactful clinical development programs and collaborate with cross-functional teams in a dynamic, science-driven environment.
Job Requirements:
- Provide statistical expertise across clinical trial design, analysis, and reporting.
- Develop and review Statistical Analysis Plans (SAPs).
- Conduct statistical analyses using SAS or R.
- Interpret and communicate findings to internal and external stakeholders.
- Ensure compliance with MHRA, EMA, and FDA regulatory standards.
Experience needed:
- Proven experience as a Biostatistician in pharma or CRO settings.
- Strong knowledge of clinical trial methodology and regulatory frameworks.
- Proficiency in SAS and/or R.
- MSc or PhD in Biostatistics, Statistics, or a related field.
- UK-based and eligible to work as a contractor.
Freelance Biostatistician employer: LinkedIn
Contact Detail:
LinkedIn Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Freelance Biostatistician
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who work as Biostatisticians. Attend relevant conferences or webinars to meet potential colleagues and learn about job openings that may not be advertised.
✨Tip Number 2
Join online forums and groups focused on biostatistics and clinical trials. Engaging in discussions can help you stay updated on industry trends and may lead to job referrals from fellow members.
✨Tip Number 3
Consider reaching out directly to hiring managers or team leads at companies you're interested in. A well-crafted message expressing your interest and relevant experience can make a strong impression.
✨Tip Number 4
Stay current with the latest statistical software updates and methodologies. Being proficient in SAS and R is crucial, so consider taking short courses or certifications to enhance your skills and demonstrate your commitment to continuous learning.
We think you need these skills to ace Freelance Biostatistician
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience as a Biostatistician, particularly in pharmaceutical or CRO settings. Emphasise your proficiency in SAS and R, and include any relevant projects that demonstrate your statistical expertise.
Craft a Strong Cover Letter: Write a cover letter that specifically addresses the job requirements. Mention your experience with clinical trial design, analysis, and reporting, and how you ensure compliance with regulatory standards like MHRA, EMA, and FDA.
Showcase Your Technical Skills: In your application, provide examples of how you've developed and reviewed Statistical Analysis Plans (SAPs). Highlight any specific statistical analyses you've conducted and the impact of your findings on previous projects.
Prepare for Communication: Since the role involves interpreting and communicating findings to stakeholders, consider including examples of how you've effectively communicated complex statistical concepts to non-statistical audiences in your application.
How to prepare for a job interview at LinkedIn
✨Showcase Your Statistical Expertise
Be prepared to discuss your experience with statistical analysis in detail. Highlight specific projects where you developed or reviewed Statistical Analysis Plans (SAPs) and how your contributions impacted the outcomes.
✨Familiarise Yourself with Regulatory Standards
Understand the compliance requirements of MHRA, EMA, and FDA. Be ready to explain how you have ensured adherence to these standards in your previous roles, as this will demonstrate your knowledge of the regulatory landscape.
✨Demonstrate Proficiency in SAS or R
Since proficiency in SAS or R is crucial for this role, be prepared to discuss your experience with these tools. You might even want to bring examples of analyses you've conducted using these software packages to illustrate your skills.
✨Communicate Findings Effectively
Practice explaining complex statistical concepts in simple terms. The ability to communicate findings to both technical and non-technical stakeholders is key, so think of examples where you successfully conveyed your results.