Senior Statistical Programmer

Location United States of America
Discipline: Biometrics
Job type: Permanent
Salary: £Salary Range - $115,000-125,000
Contact name: Dan Sidell

Contact email: dan.sidell@rbwconsulting.com
Contact phone: 6179821238
Job ref: 22261 - Snr
Published: about 1 month ago
Expiry date: 22 October 2021

Senior Statistical Programmer

Location: Fully Remote

Several Senior Statistical Programmers roles available with a leading CRO that CAN sponsor H1B Visa’s!

Exciting opportunity to join a top company in one of many prolific groups! Looking for candidates who have experience leading projects.

Duties:

You will provide technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to the analysis and reporting of clinical study data. In addition, liaise with sponsors, Data Operations Leads, and other functional areas as required.

  • Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to.

  • Lead a statistical programming team to successful completion of a study within given timelines and budget

  • Monitor project resourcing, project budgets, and identify changes in scope

  • Interact with Sponsors as the key contact regarding statistical programming issues

  • Provide technical support and advice to the internal team

  • Check own work in an ongoing way to ensure first-time quality

  • Ensure quality control (QC) on all process and technical activities related to derived dataset, table, listing, and figure programming in accordance with corporate quality standards, WSOPs/Guidelines, ICH-GCP and/or other international regulatory requirements are performed.

Job Qualifications :

  • Educated to a degree level (biological science, pharmacy or other health related discipline preferred) or relevant clinical or business equivalent

  • 5 plus years proficiency in SAS programming

  • 2+ years of ADaM, CDISC or SDTM

  • Lead experience within clinical trials

  • Attention to detail, ability to be self-driven and solid organization skills

  • Excellent communication skills (verbal and written)