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Statistical Programmer II - Sponsor Dedicated (FSP)

CTI Clinical Trial and Consulting Services

Maidenhead

Remote

GBP 40,000 - 60,000

Full time

Today
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Job summary

A leading global contract research organization is seeking a Statistical Programmer II to support complex clinical trials. The role involves programming, leading studies, and creating datasets crucial for regulatory submissions. Offering flexible working arrangements, this position is ideal for motivated individuals eager to make a significant impact in clinical research.

Qualifications

  • Minimum Bachelor’s degree in a relevant field.
  • 1-2 years of SAS programming experience in a CRO or Pharmaceutical industry.
  • Knowledge of CDISC requirements.

Responsibilities

  • Lead programming activities for complex clinical trials.
  • Develop and maintain SAS programs for SDTM and ADaM datasets.
  • Produce analysis results and documentation.

Skills

SAS programming
Data management
Statistical analysis

Education

Bachelor's degree in mathematics, statistics, computing, life science, or health science

Job description

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

As a Statistical Programmer II in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests.

You can be 100% home-based or if you prefer, you can work from our local office in your home country.

Your Responsibilities

  • With sufficient experience assume the role of a Lead Statistical Programmer for CP studies only with support from senior programming staff
  • Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and the client, etc.
  • Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs
  • Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated eCRFs and Reviews Guides to support SDTMs and ADaMs
  • With support from senior programming staff, develop specifications for SDTMs and ADaM datasets
  • Review SAPs and TFL shells from a programming perspective for studies with support from senior programming staff
  • Respond to QA and client audits with support from senior programming staff
  • And all other duties as needed or assigned

Your Profile

  • Minimum Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects
  • Typically, 1 - 2 years of SAS programming experience in the CRO or Pharmaceutical industry, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
  • Knowledge of CDISC requirements
  • Business fluency in English – both spoken and written – is a must

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

Fortrea Is Proud To Be An Equal Opportunity Employer

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does 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. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.

If you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: . Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.

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