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Statistical Clinical Programmer (Temporary)
Remote • Clinical
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Description

*Note: this is temporary contract position lasting 6 months with the possibility of extension. Preference will be given to candidates based in San Diego, CA. *


Company Overview:


Vividion is a next generation biotechnology company based in San Diego that is leveraging its proprietary chemical proteomics platform to conduct proteome-wide footprinting of drug-protein interactions with unprecedented breadth and precision. Our technology allows us to screen, identify and optimize novel drugs that selectively bind virtually any protein, including proteins previously considered “undruggable”.  Our pipeline and emerging programs reflect a matured and productive platform capable of delivering first in class drugs utilizing novel mechanisms of action (allosteric inhibitors, protein-protein interaction inhibitors, functional activators, degraders etc.) against undruggable targets in the oncology and immunology space.


Vividion has been recognized as a Top Workplace by The San Diego Union-Tribune in 2022, 2023, and 2024.


Job Summary:


Statistical Programmer is responsible for providing statistical programming support using SAS or R to the clinical trial team.

Requirements

Essential Duties and responsibilities:

  • Provides comprehensive programming support to clinical project teams including Ad-hoc requests, SDTM/AdaM/TFL programming using SAS and comply with regulatory requirements, programming SOP and Working procedure.
  • QC CRO SDTM and ADaM data sets, tables, listings, and figures following CDISC standards for clinical trials for multiple studies. 
  • Reviews key planning documents (e.g., statistical analysis plan, mock shells, data review plan) to align with project objectives and ensures clarity and completeness of programming tasks; 
  • Independently develops, validates, troubleshoots, and maintains complex programs and utilities in accordance with predefined specifications and standards.
  • Develops unambiguous and robust programming specifications (e.g. ADaM specifications) for multiple studies
  • Demonstrates advanced knowledge of CDISC standards, medical terminology, clinical trial methodologies, and FDA/ICH regulations.
  • Communicates proactively and effectively around issues and risks and contributes to its remediation.
  • Provides visualization outputs using R programming to clinical development team

Qualifications:

  • Bachelor’s or MS degree in statistics, biostatistics, mathematics, computer science or life sciences required
  • Proficient in R and SAS language
  • At least 8 years programming experience in industry including support of significant regulatory filings
  • Proficient knowledge of programming in the analysis and submission of clinical data
  •  Broad expertise in statistical programming and in developing computing strategies
  • In-depth understanding of clinical data structure (e.g. CDISC standards) and relational databases
  • Demonstrated proficiency in using SAS to produce analysis datasets and TFLs and in using other software tools and applications (e.g. MS office, XML, Pinnacle 21)
  • Demonstrated ability in processing of upstream data (e.g. multiple data forms, workflows, eDC, SDTM); 

Pay:  


The hourly pay for this position ranges from $50.00 to $90.00 depending on relevant skills, competencies, experience, and education. 


EEO & Employment Eligibility:


Vividion Therapeutics, Inc. is an equal opportunity employer. All applicants will receive consideration for employment without regard to disability or veteran status.


Privacy Policy:


The protection of your personal information is a commitment we take seriously. For information regarding our Privacy Policy (CA candidates) please visit https://vividion.com/publication/privacy-noticeforcalifornia-candidates/.

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