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- Tasks: Provide statistical expertise for clinical trials and communicate findings effectively.
- Company: Join a leading pharmaceutical company making a difference in healthcare.
- Benefits: Enjoy flexible working arrangements and the chance to work on impactful projects.
- Why this job: Be part of a dynamic team driving innovation in clinical development.
- Qualifications: MSc or PhD in Biostatistics; experience with SAS or R required.
- Other info: This is a contract role, perfect for those looking to make an impact.
The predicted salary is between 48000 - 84000 £ 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: Walker Cole International
Contact Detail:
Walker Cole International 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. Attend relevant conferences or webinars where you can meet potential colleagues and employers. Engaging with others in your field can lead to job opportunities that may not be advertised.
✨Tip Number 2
Showcase your expertise in SAS and R through online platforms like GitHub or personal blogs. Sharing your projects or analyses can demonstrate your skills to potential employers and set you apart from other candidates.
✨Tip Number 3
Familiarise yourself with the latest regulatory standards from MHRA, EMA, and FDA. Being well-versed in these guidelines will not only enhance your knowledge but also show potential employers that you are proactive and committed to compliance.
✨Tip Number 4
Prepare for interviews by practising how to communicate complex statistical findings clearly and concisely. Role-playing with a friend or mentor can help you articulate your thoughts effectively, which is crucial when discussing results with stakeholders.
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 Relevant Skills: In your application, clearly outline your skills in developing and reviewing Statistical Analysis Plans (SAPs). Provide examples of how you've communicated findings to stakeholders in previous roles.
Highlight Educational Background: Include your MSc or PhD in Biostatistics, Statistics, or a related field prominently in your application. This will help demonstrate your academic qualifications and reinforce your suitability for the role.
How to prepare for a job interview at Walker Cole International
✨Showcase Your Statistical Expertise
Be prepared to discuss your experience with statistical analyses 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've 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 them to illustrate your skills.
✨Communicate Findings Effectively
Practice explaining complex statistical concepts in simple terms. During the interview, you may need to demonstrate how you would communicate findings to both technical and non-technical stakeholders, so clarity is key.
