Senior Statistician
1 week ago
Join to apply for the Senior Statistician - USA/Canada - Remote role at Worldwide Clinical Trials 3 days ago Be among the first 25 applicants Join to apply for the Senior Statistician - USA/Canada - Remote role at Worldwide Clinical Trials Who We AreWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. Who We AreWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.Why WorldwideWe believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join usWhat Biostatistics Department Does At WorldwideAs an individual on our Biostats and Statistical Programming team, your programming, analytical skills, and ability to process and interpret data are the keys to success. At Worldwide, you’ll be able to grow your knowledge of SAS and CDISC standards across all phases of clinical trials. You’ll work directly with multiple sponsors, data managers, statisticians, statistical programmers, and the wider study team across a variety of therapeutic areas including cardiovascular, metabolic, neuroscience, oncology & rare diseases. When you work here, you have the autonomy to do your work through hands-on involvement, the support you need to succeed and grow, and the realization that, here, your work really does matter.What You Will DoManage the statistics support to one or more projects/sponsor programmes of work, ensuring that needs are fully met by expert and timely statistical consultancy and support. Provides expert review of study designs, analysis plans and reports. Assist sponsors in the design of clinical trials, including statistical sections of the study protocol, randomisation methodology and writing statistical analysis plans. Liaise with internal departments, sponsors and other third parties regarding statistical issues and reporting requirements. Provide project support to the statistics reporting process through the specification/review of tables, figures and listings shells, writing/review of derived dataset specifications and the formatting of report documents and tabulations. Undertake the preparation of final reports, including the production of tables, listings and figures, and report writing. Develop, test and run SAS programs for the statistical analysis and reporting of clinical study data. This includes programs for derived datasets, CDISC (SDTM and ADaM) datasets, tables, figures and listings and their validation. Ensure the maintenance of documentation e.g. the description of programs and validation Produce ad hoc data summaries when requested during the course of a trial. Extract information from the system during the course of a trial e.g. summaries, data listings, study data sets. Validate software, in the role of system owner or tester, and test SAS Macros, maintaining the required validation and testing documentation. What You Will Bring To The RoleThe job holder must be computer literate and numerate with a proven ability to adapt to various computer systems Hands-on expert level project statistician experienced in providing statistical leadership to projects. Design and analysis consultancy skills and knowledge across a broad range of applications together with key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change. Your ExperienceEducated to degree level in mathematics, statistics or another subject with a strong statistical component. 4+ years of industry experience in a CRO, Pharmaceutical or Biotechnology company as a statistician, ideally working in phases II & III. We love knowing that someone is going to have a better life because of the work we do.To view our other roles, check out our careers page at Discover a world of difference at Worldwide For more information on Worldwide, visit or connect with us on LinkedIn.Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Research Services Referrals increase your chances of interviewing at Worldwide Clinical Trials by 2x Sign in to set job alerts for “Senior Statistician” roles. We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr
-
Senior Statistician
2 weeks ago
Toronto, Montreal, Calgary, Vancouver, Edmonton, Old Toronto, Ottawa, Mississauga, Quebec, Winnipeg, Halifax, Saskatoon, Burnaby, Hamilton, Surrey, Victoria, London, Halton Hills, Regina, Markham, Brampton, Vaughan, Kelowna, Laval, Southwestern Ontario, R, Canada worldwide.com Full timeSenior Statistician - USA/Canada - Remote page is loaded## Senior Statistician - USA/Canada - Remoteremote type: Remotelocations: Virtual Canada Ontario: Durham, North Carolina: Quebec, Canada: Ontario, Canadatime type: Full timeposted on: Posted 30+ Days Agojob requisition id: JR100667**Who we are**We’re a global, midsize CRO that pushes...
-
Senior Statistician
3 weeks ago
Toronto, Montreal, Calgary, Vancouver, Edmonton, Old Toronto, Ottawa, Mississauga, Quebec, Winnipeg, Halifax, Saskatoon, Burnaby, Hamilton, Victoria, Surrey, Halton Hills, London, Regina, Markham, Brampton, Vaughan, Kelowna, Laval, Southwestern Ontario, R, Canada Mercor Full timeA leading AI research organization is seeking a Senior Statistician to serve as an AI tutor in statistics. The role entails ensuring data annotation quality and statistical rigor across AI models. Qualified candidates should have a Master's or PhD in Statistics or Mathematics, with strong analytical and research skills. The position offers a salary range of...
-
Senior Biostatistician
4 weeks ago
Quebec, Canada Veristat Full timeJoin to apply for the Senior Biostatistician role at Veristat.OverviewThe Senior Biostatistician provides statistical input into Phase I‑IV clinical trial development, performs analysis of clinical trial, and contributes to reporting of clinical trial results. This role can work independently and function as a lead statistician on clinical...
-
Senior Biostatistician
3 weeks ago
Quebec, Canada Veristat Full timeJoin to apply for the Senior Biostatistician role at Veristat.OverviewThe Senior Biostatistician provides statistical input into Phase I‑IV clinical trial development, performs analysis of clinical trial, and contributes to reporting of clinical trial results. This role can work independently and function as a lead statistician on clinical...
-
Senior Biostatistician
3 weeks ago
Quebec, Canada Veristat Full timeJoin to apply for the Senior Biostatistician role at Veristat . Overview The Senior Biostatistician provides statistical input into Phase I‑IV clinical trial development, performs analysis of clinical trial, and contributes to reporting of clinical trial results. This role can work independently and function as a lead statistician on clinical trials....
-
Senior Biostatistician
4 weeks ago
Toronto, Montreal, Calgary, Vancouver, Edmonton, Old Toronto, Ottawa, Mississauga, Quebec, Winnipeg, Halifax, Saskatoon, Burnaby, Hamilton, Victoria, Surrey, Halton Hills, London, Regina, Markham, Brampton, Vaughan, Kelowna, Laval, Southwestern Ontario, R, Canada Veristat Full timeSenior Biostatistician – Veristat Job Description The Senior Biostatistician provides statistical input into Phase I - IV clinical trial development, performs the analysis of clinical trial data, and provides statistical input into the reporting of clinical trial results. The Senior Biostatistician can work independently and function as a lead statistician...
-
Senior Biostatistician
3 weeks ago
Toronto, Montreal, Calgary, Vancouver, Edmonton, Old Toronto, Ottawa, Mississauga, Quebec, Winnipeg, Halifax, Saskatoon, Burnaby, Hamilton, Victoria, Surrey, Halton Hills, London, Regina, Markham, Brampton, Vaughan, Kelowna, Laval, Southwestern Ontario, R, Canada Alira Health Group Full timeSenior Biostatistician page is loaded## Senior Biostatisticianremote type: Remotelocations: Boston-Remote: Toronto-Remotetime type: Full timeposted on: Posted Todayjob requisition id: JR000436If so, please apply using the referral link emailed to you.Join our global team dedicated to innovation and initiative, where physical walls and different...
-
Principal Statistician
4 weeks ago
Toronto, Montreal, Calgary, Vancouver, Edmonton, Old Toronto, Ottawa, Mississauga, Quebec, Winnipeg, Halifax, Saskatoon, Burnaby, Hamilton, Victoria, Halton Hills, Surrey, London, Regina, Markham, Brampton, Vaughan, Kelowna, Laval, Southwestern Ontario, W, Canada Warman O'Brien Full timeGet AI-powered advice on this job and more exclusive features. FSP Principal Biostatistician – Early Phase Clinical Development (PK) | Home-based | Canada | Permanent We are working with a leading global CRO who have an opportunity within their FSP team for a Senior or Principal Biostatistician to provide statistical support for early-phase drug...
-
Consultant principal, statisticien
2 weeks ago
Toronto, Montreal, Calgary, Vancouver, Edmonton, Old Toronto, Ottawa, Mississauga, Quebec, Winnipeg, Halifax, Saskatoon, Burnaby, Hamilton, Surrey, Victoria, London, Halton Hills, Regina, Markham, Brampton, Vaughan, Kelowna, Laval, Southwestern Ontario, R, Canada IQVIA Full timePRÉSENTATION Les conseillers principaux sont des responsables de l’exécution de projets chargés de mettre en œuvre une recherche de synthèse des données probantes méthodologiquement rigoureuse, de superviser le travail du personnel subalterne et de gérer l’ensemble du projet. Ils travaillent de manière indépendante et en équipe, agissent sur...
-
Remote Senior Statistician: Clinical Trials
2 weeks ago
Calgary, Toronto, Montreal, Vancouver, Edmonton, Old Toronto, Ottawa, Mississauga, Quebec, Winnipeg, Halifax, Saskatoon, Burnaby, Hamilton, Surrey, Victoria, London, Halton Hills, Regina, Markham, Brampton, Vaughan, Kelowna, Laval, Southwestern Ontario, R, Canada Alimentiv Inc. Full timeA global research organization is seeking a statistical expert to support clinical trials in Calgary, Canada. Responsibilities include statistical analysis, data management, and guidance throughout the project lifecycle. The ideal candidate has a Bachelor's or Master's degree, with 1-3 years of relevant experience. This home-based position offers a...