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Senior Statistical Programmers

This role is for two Senior Statistical Programmers with 12+ months renewable contract, remote work in Pacific hours. Key skills include SAS, oncology submissions, and data integration. Requires 12-15+ years experience, preferably with solid tumor expertise and late-phase submissions.
🌎 - Country
United States
💱 - Currency
$ USD
💰 - Day rate
Unknown
Unknown
🗓️ - Date discovered
February 19, 2025
🕒 - Project duration
More than 6 months
🏝️ - Location type
Remote
📄 - Contract type
Unknown
🔒 - Security clearance
Unknown
📍 - Location detailed
United States
🧠 - Skills detailed
#REST (Representational State Transfer) #Programming #ADaM (Analysis Data Model) #Consul #SAS #Data Integration
Role description
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SENIOR STATISTICAL PROGRAMMER (2 OPENINGS)

12+ MONTHS RENEWABLE

LOCATION: Work will be performed remotely. The company is based in CA, core Pacific working hours must be accommodated.

Summary

A clinical-stage biotech company in the Bay area is in need of two Senior Statistical Programmers to support the team on a long-term basis. This organization is dedicated to the development of oncological therapeutics. With a growing pipeline, the workload is picking up, and the Programming team needs more support.

These consultants must have strong oncology submissions experience, preferably solid tumor experience. The best individuals for these opportunities will thrive in a fast-paced environment, be willing to wear multiple hats, and have excellent communication skills. They will be a part of a very experienced team and must be able to work well both independently and with the rest of the team with a high degree of independence and decision-making.

Qualifications & Requirements
• 12-15+ years of statistical programming experience (small-mid sized sponsor company experience is preferred)
• Oncology expertise is required; preferable to have solid tumor experience and an understanding of RECIST criteria
• Late-phase oncology submissions experience
• Able to independently develop SAS programs and specifications (SDTM, ADaM), for use in study or other analyses
• Experience with data integration used for clinical summaries and/or creation and quality control of statistical submission components to regulatory agencies
• Experience creating and maintaining listings, tabulations, graphical summaries, and formal statistical estimates and tests.
• Excellent understanding and review of CRFs/CRF specs, protocols, etc.