Senior Statistician - USA/Canada - Remote

Worldwide Clinical Trials; Durham (NC); Remote; USD 90,000 - 120,000; Full time

Job summary

A leading global CRO seeks a Senior Statistician to manage statistical support for projects and contribute to clinical trial designs. The ideal candidate will have strong analytical skills, leadership experience, and a degree in mathematics or statistics. Join a diverse team committed to improving patients' lives.

Qualifications

• At least 4 years of industry experience in a CRO, pharmaceutical, or biotech company.
• Strong statistical component in education.

Responsibilities

• Manage statistical support for projects.
• Review study designs and analysis plans.
• Develop and run SAS programs for data analysis.

Skills

Leadership

Analytical Skills

Customer Focus

Innovative Mindset

Education

Degree in Mathematics

Degree in Statistics

Tools

SAS

Job description

Join to apply for the Senior Statistician - USA/Canada - Remote role at Worldwide Clinical Trials

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, a global team of over 3,500 experts, bright thinkers, dreamers, and doers, 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. We value diversity and inclusion, fostering a supportive environment where everyone can thrive and do their best work.

What the Biostatistics Department Does at Worldwide

As part of our Biostats and Statistical Programming team, your programming, analytical skills, and data interpretation abilities are key to success. You will grow your SAS and CDISC knowledge across all clinical trial phases, working directly with sponsors, data managers, statisticians, and the wider study team across various therapeutic areas.

What You Will Do

1. Manage statistical support for projects, ensuring expert and timely consultancy.
2. Review study designs, analysis plans, and reports.
3. Assist in designing clinical trials, including statistical sections and analysis plans.
4. Liaise with internal departments, sponsors, and third parties regarding statistical issues.
5. Support reporting processes, including tables, figures, listings, and report writing.
6. Develop, test, and run SAS programs for data analysis and reporting.
7. Maintain documentation of programs and validation.
8. Produce ad hoc data summaries and extract information during trials.
9. Validate software and maintain validation documentation.

What You Will Bring to the Role

• Computer literate and numerate with adaptability to various systems.
• Experienced project statistician with leadership skills.
• Strong design and analysis consultancy skills, with customer focus and innovative mindset.

Your Experience

• Degree in mathematics, statistics, or a related field with a strong statistical component.
• At least 4 years of industry experience in a CRO, pharmaceutical, or biotech company, preferably in phases II & III.

Additional Information

We are committed to diversity and equal opportunity. Join us to make a difference in patients' lives.

Job Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Research, Analysis, IT
• Industry: Research Services