Senior Statistical Programmer

4 weeks ago


Maidenhead, Windsor and Maidenhead, United Kingdom Fortrea Full time

Fortrea is 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 with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.

As a Lead Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you will be central to the successful delivery of complex oncology projects for a renowned, innovative, and global top pharmaceutical company. You will liaise with the entire study team as needed, including Clinical, Medical Writing, Safety, and Biometrics.

This is a great opportunity to see how clinical trials work from a Big Pharma perspective while being part of a global CRO with opportunities for future career growth. You can work 100% from home in EMEA or from our local office in your home country.

We offer highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, and remote working allowances. You will also enjoy a genuine work-life balance, a permanent employment contract, excellent training and career development opportunities, and strong support from your Line Manager and team.

Key responsibilities include planning, executing, and overseeing all programming activities on a study, including resource estimation, working within budget, meeting timelines, maximizing quality, and interaction with other departments. You will also liaise with other Sponsor departments for additional programming needs, ensure all activities are conducted efficiently, and prioritize quality at all times.

Requirements include a degree in a relevant field such as mathematics, life sciences, statistics, or computer sciences, or professional experience in statistical programming within clinical trials in a biotech, CRO, or pharmaceutical company. Solid experience with complex clinical trials and the corresponding datasets' content is also required. Expert knowledge of base SAS, SAS macros, SAS/STAT, and debugging SAS programs is essential. Fluency in English is a must.

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. We strive for diversity and inclusion in the workforce and do not tolerate harassment or discrimination of any kind.



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