At a Glance
- Tasks: Lead statistical analysis for clinical trials and ensure data quality.
- Company: Join an award-winning CRO known for its supportive and innovative culture.
- Benefits: Enjoy a competitive salary, remote work, and career advancement opportunities.
- Other info: Be part of a dynamic environment with excellent employee retention and satisfaction.
- Why this job: Make a real impact in clinical research while working with a collaborative team.
- Qualifications: Master's or PhD in statistics with relevant experience and strong SAS skills.
The predicted salary is between 55000 - 70000 £ per year.
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognised for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Senior Biostatistician Roles & Responsibilities
- Provides advanced input into statistical sections and overall consistency of clinical study protocols.
- Develops and reviews statistical analysis plans (SAP).
- Determines appropriate analyses for clinical endpoints based on input from the protocol and the client.
- Performs senior-level reviews and is responsible for the datasets and outputs of a project.
- Ensures consistency with the SAP and reviews for correctness and quality.
- Works with programming team to provide definitions for analysis/ADaM datasets to be used for final analyses.
- Develops specifications and reviews datasets based on what is needed for the planned tables, listings and graphs (TLGs).
- Prepares TLG shells/specifications and programming notes based on SAP and analysis/ADaM datasets.
- Works with data management team to review data collection (e.g., CRFs) and helps ensure data quality throughout the clinical trial.
- Performs and/or coordinates the preparation, execution, reporting and documentation of high-quality statistical analysis according to the SAP.
- Provides high level of support to the programmers and medical writers on all statistical matters according to client requirements.
- Prepares and reviews statistical methods and results sections for the clinical study report (CSR) with in-house medical writers.
- Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician.
- Generates sample size calculations appropriate for the primary endpoint and based on input from the protocol.
- Generates and reviews randomization schedules per the protocol and randomization specifications.
- Works with the project management group to ensure timelines are appropriate given the scope of the project.
- Is familiar with and stays current with the latest industry practices and updated regulatory guidelines.
- Communicates competently and independently with client to coordinate the statistical and programming considerations of the project.
- Demonstrates strong understanding of ICH guidelines, as applicable to statistics.
- Practices good internal and external customer service.
Requirements
- Master of Science (in statistics or equivalent) with five (5) plus years relevant work experience or PhD (in statistics or equivalent) with two (2) plus years of relevant work experience.
- Strong knowledge of and experience with SAS (SAS Stat, SAS Base, SAS macros, SAS/ODS, SAS/Graph).
- Able to be in a hands-on role by digging into data and using SAS to validate datasets and outputs.
- Excellent mathematical and problem-solving skills.
- Advanced knowledge of the statistical considerations involved in drug development including hands-on experience with clinical trial data.
- Strong knowledge of study designs and statistical analysis methods (e.g., GLMs, non-parametric methods, survival analysis techniques, general imputation methods, common descriptive stats).
- Strong familiarity with a variety of clinical data and databases (including EDC systems).
- Working knowledge of SDTM/ADaM standards (in the absence of ADaM experience, considerable experience working with analysis or derived datasets).
- At least three (3) years of experience in pharmaceutical industry.
- Ability to coordinate the analytical aspects of multiple projects or clinical trials at the same time.
- Proficiency with MS Office applications (e.g., Word, PowerPoint and Excel).
- Good interpersonal, oral, and written communication skills.
- Self-motivated, hardworking, dependable, and positive team-oriented personality.
- Ability to communicate effectively and provide clear directions to Statistical Programmers.
Senior Biostatistician - Remote (UK) Biometrics LONDON, ENGLAND, UNITED KINGDOM employer: MMS Holdings Inc
MMS is an award-winning clinical research organisation that values your contributions and fosters a supportive, innovative work culture. With a Great Place to Work certification and a commitment to employee growth, we offer exceptional opportunities for career advancement in a collaborative environment, all while working remotely from the UK. Join us to be part of a team that is shaping the future of clinical research and enjoy the benefits of a company that prioritises employee satisfaction and retention.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Biostatistician - Remote (UK) Biometrics LONDON, ENGLAND, UNITED KINGDOM
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant webinars, and join online forums. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to biostatistics. Use the STAR method (Situation, Task, Action, Result) to structure your answers and showcase your experience effectively.
✨Tip Number 3
Showcase your skills with a portfolio! If you’ve worked on interesting projects or analyses, compile them into a portfolio to share during interviews. This gives potential employers a tangible sense of what you can bring to the table.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our awesome team at MMS.
We think you need these skills to ace Senior Biostatistician - Remote (UK) Biometrics LONDON, ENGLAND, UNITED KINGDOM
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Biostatistician role. Highlight your relevant experience with SAS and clinical trial data, and don’t forget to showcase your problem-solving skills. We want to see how your background aligns with what we do at MMS!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about biostatistics and how you can contribute to our innovative team. Be sure to mention any specific projects or experiences that relate to the responsibilities outlined in the job description.
Showcase Your Communication Skills:As a Senior Biostatistician, you'll need to communicate complex statistical concepts clearly. In your application, demonstrate your written communication skills by being concise and clear. We appreciate candidates who can convey their thoughts 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, you’ll get to explore more about our culture and values while you’re there!
How to prepare for a job interview at MMS Holdings Inc
✨Know Your Stats Inside Out
As a Senior Biostatistician, you'll need to demonstrate your expertise in statistical methods and clinical trial data. Brush up on key concepts like GLMs, survival analysis techniques, and the latest ICH guidelines. Be ready to discuss how you've applied these in past projects.
✨Showcase Your SAS Skills
Since strong knowledge of SAS is crucial for this role, prepare to talk about your hands-on experience with SAS Stat, Base, and macros. Consider bringing examples of datasets you've validated or analyses you've performed using SAS to illustrate your capabilities.
✨Understand the Company Culture
MMS prides itself on its supportive and innovative culture. Research their values and think about how your personal work style aligns with their collaborative environment. Be prepared to share examples of how you've thrived in team settings or contributed to a positive workplace.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about the role, team dynamics, and ongoing projects at MMS. This shows your genuine interest in the position and helps you assess if it's the right fit for you.
