Statistical Programmer

4 weeks ago

Maidenhead, Windsor and Maidenhead, United Kingdom Pharmiweb Full time
Job Title: Statistical Programmer - Clinical Trials Specialist

About the Role:

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, we provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, we are transforming drug and device development for partners and patients across the globe.

Key Responsibilities:

- Develop and validate SAS and R programs for data presentations and analyses
- Provide programming support to your multidisciplinary global project team
- Participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as chronic and rare diseases

Requirements:

- Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.
- Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company
- Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs
- Programming experience in R is required
- Proven professional experience with SDTMs, ADaM datasets (safety and efficacy) and TFLs
- Solid knowledge of CDISC standards
- Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail
- Business fluency in English - both spoken and written - is a must

What We Offer:

- Rewarding and meaningful work in an established, diverse, highly profitable and respected global company
- Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
- A genuine work life balance
- Flexibility in working hours
- A thorough onboarding with support from your personal mentor
- A permanent employment contract with us
- Excellent training and career development opportunities, as well as support with advancing your individual education
- Strong support from your Line Manager and your team, as well as from more than 20,000 colleagues worldwide

Work Environment:

This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as chronic and rare diseases. Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day.

Requirements for the Role:

- In this role, programming experience in R and SAS is required.
- In this role, you can be 100% home-based or you can work from our local offices.

What Else Can You Expect from Us?

- Rewarding and meaningful work in an established, diverse, highly profitable and respected global company
- Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
- A genuine work life balance
- Flexibility in working hours
- A thorough onboarding with support from your personal mentor
- A permanent employment contract with us
- Excellent training and career development opportunities, as well as support with advancing your individual education
- Strong support from your Line Manager and your team, as well as from more than 20,000 colleagues worldwide

Equal Opportunity Employer:

As an EOE/AA employer, we strive for diversity and inclusion in the workforce and do not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

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