At a Glance
- Tasks: Lead statistical analysis for oncology studies, ensuring data quality and accuracy.
- Company: ClinChoice is a global CRO focused on quality and professional development in clinical research.
- Benefits: Enjoy remote work flexibility, career growth opportunities, and a supportive team culture.
- Why this job: Join a mission-driven company that values diversity and offers impactful work in drug development.
- Qualifications: MS or PhD in Statistics/Biostatistics with relevant experience in clinical trials and FDA regulations.
- Other info: Be part of a diverse team committed to innovation and excellence in healthcare.
The predicted salary is between 48000 - 84000 £ per year.
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. ClinChoice is searching for a Senior Statistician Consultant- Onco Late Phase to join one of our clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client's counterparts.
Main Job Tasks and Responsibilities:
- Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.
- Provide statistical oversight to studies and assure adequate quality and consistency with project requirements.
- Responsible for assuring that data for statistical analyses are complete, accurate and consistent.
- Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions.
- Responsible for validity of analysis and explore alternative analysis strategies as needed.
- Demonstrates extensive understanding of statistical concepts and methodologies.
- Recognizes and corrects flaws in scientific reasoning and statistical interpretation.
- Responsible for accuracy and consistency of statistical tables, figures, and data listings, accuracy of report text, and consistency between summary tables in the body of reports and the corresponding source tables and listings.
- Responsible for statistical methods section for the reports.
- Identifies and corrects common flaws in interpretation of results, inconsistency in presentation or inference, adherence to the report guidelines, and assures project-wide consistency.
- Effectively mentor peers with regards to statistical methodology and provide appropriate training to less experienced statisticians.
- Manage activities of statisticians across projects by appropriately coordinating assignments and reviewing work so that projects are delivered on time with high quality.
Education and Experience:
- MS or PhD in Statistics, Biostatistics or related field.
- PhD with 2-4 years of experience or MS with 4-6 years of experience.
- Strong oral and written communications skills, with ability to effectively communicate internally and with clients.
- Demonstrated understanding and insight in statistics, drug development process and relevant FDA regulations.
- Pharmaceutical, CRO, or related industry experience with clinical trials, including interaction with Regulatory Agencies, especially FDA.
The Application Process:
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
About ClinChoice:
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos:
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK) employer: CROMSOURCE
Contact Detail:
CROMSOURCE Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land #699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK)
✨Tip Number 1
Familiarise yourself with the latest statistical methodologies and tools relevant to oncology. Being well-versed in these areas will not only boost your confidence during interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals in the CRO and pharmaceutical industries, especially those who have experience in late-phase oncology studies. Engaging in discussions or attending industry events can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples from your past work that showcase your ability to manage statistical analysis plans and mentor junior statisticians. Real-life scenarios will help illustrate your expertise and problem-solving skills to potential employers.
✨Tip Number 4
Research ClinChoice's recent projects and their approach to statistical oversight in clinical trials. Tailoring your conversation to reflect an understanding of their work will show your genuine interest in the role and the company.
We think you need these skills to ace #699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in statistics, biostatistics, and clinical trials. Emphasise your skills in protocol development, statistical analysis plans, and any experience with FDA regulations.
Craft a Strong Cover Letter: Write a cover letter that showcases your understanding of the role and the company. Mention your ability to work independently and establish trust with clients, as well as your mentoring experience with less experienced statisticians.
Highlight Relevant Education: Clearly state your educational qualifications, especially if you hold an MS or PhD in Statistics or Biostatistics. Include any specific coursework or projects that relate to late-phase oncology studies.
Showcase Communication Skills: Since strong oral and written communication skills are essential for this role, provide examples in your application where you've effectively communicated complex statistical concepts to non-experts or collaborated with cross-functional teams.
How to prepare for a job interview at CROMSOURCE
✨Showcase Your Statistical Expertise
Be prepared to discuss your understanding of statistical concepts and methodologies in detail. Highlight specific examples from your past experience where you successfully applied these skills, especially in the context of late-phase oncology studies.
✨Demonstrate Client-Facing Skills
Since this role involves direct interaction with clients, practice articulating how you've built trust and rapport in previous roles. Share anecdotes that illustrate your ability to communicate complex statistical information clearly and effectively.
✨Prepare for Technical Questions
Expect questions related to protocol development, sample size calculations, and statistical analysis plans. Brush up on relevant FDA regulations and be ready to discuss how you've ensured data accuracy and consistency in your previous projects.
✨Emphasise Mentorship Experience
If you have experience mentoring less experienced statisticians, make sure to highlight this during the interview. Discuss how you've provided training and guidance, and how this has contributed to project success and team development.