Senior Statistician - USA / Canada - Remote

Worldwide Clinical Trials; Quebec; Remote; CAD 80,000 - 120,000; Full time

Job summary

Join a leading global CRO as a Senior Statistician, contributing to high-impact clinical trials. In this remote role, leverage your statistical expertise to support project teams and enhance data quality through SAS programming. A degree in mathematics or statistics and several years of hands-on experience in a clinical environment are essential for this mid-senior level position. Be part of a collaborative and inclusive workplace dedicated to improving patient outcomes.

Qualifications

• 4+ years in a CRO or pharmaceutical setting as a statistician.
• Hands-on expertise in project statistics.
• Experience in phases II & III clinical trials.

Responsibilities

• Manage statistical support for multiple projects.
• Provide expert review of study designs and analysis plans.
• Develop and run SAS programs for statistical analysis.

Skills

Statistical consultancy skills

Project leadership

Data interpretation

Customer focus

Communication skills

Education

Degree in mathematics or statistics

Tools

SAS

Job description

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Who We Are

We’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 Are

We’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 Worldwide

We 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 us!

What Biostatistics Department Does At Worldwide

As 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 Do

• Manage 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 Role

• The 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 Experience

• Educated 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 www.Worldwide.com 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

Research Services

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