CDISC StandardsClinical TrialsDatasetsIndustry StandardsMacrosOrganization SkillsRegulatory RequirementsSASStatistical ProgrammingStudy Data Tabulation Model
MaidenheadUK
10190+ employees
HealthcarePharmaceuticalBiotechnologyClinical Research
Role
Who you are
Review SAPs and TFL shells from a programming perspective
Develop and lead the development of complex specifications for SDTMs and ADaM datasets
Develop and maintain SAS programs for SDTM and ADaM datasets and TFLs
Produce XML/PDFs, ARM, aCRFs, and Reviewers Guides for SDTMs and ADaMs
Respond to QA and client audits
Improve clinical statistical programming business efficiency
Maintain awareness of industry standards, regulatory requirements, and SOPs
Desirables
Strong organizational skills
Curious mind
Keen attention to detail
Collaborative work style
What the job involves
Develop and validate SAS programs for data presentations and analyses
Provide programming support to a global project team
Participate in the development of benchmark drugs for chronic and rare diseases
Fortrea is a leading global provider of clinical development and patient access solutions, partnering with biopharmaceutical and medical device companies to drive healthcare innovation. Their extensive experience across over 20 therapeutic areas enables them to deliver clinical trial management and technology-enabled solutions, ensuring the accelerated delivery of life-changing therapies to patients worldwide.
Company benefits
Rewarding and meaningful work
Highly competitive compensation packages
Various local benefits such as pension contributions and health insurance plans
Remote working allowances
Work life balance
Flexibility in working hours
Thorough onboarding with personal mentor
Permanent employment contract
Excellent training and career development opportunities