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Senior Clinical Programmer - Remote

Posted 7 weeks ago
All others
Full Time
CA, USA
$155,000 - $171,000/year

Overview

The Senior Clinical Programmer will be responsible for support of team data review, data reconciliation and edit checks, and programming submission ready SDTM deliverables. This position will report to an Associate Director of Clinical Programming or higher and will interact regularly with internal and external biostatisticians, clinical data managers, and other team members. Demonstrated ability to prioritize work and to effectively communicate and collaborate with key stakeholders both within Biometrics and beyond (research, translational science, clinical science, clinical operations and regulatory) is a must.

In Short

  • Working from specifications developed by Data Management, with some support build and execute programs for internal data reviews, data reconciliation, and edit checks.
  • Assist in developing/maintaining clinical programming related standards and tools.
  • Work with data management to review case report forms, database specifications and similar documents.
  • With some support, develop data transfer specifications and manage the transfer of external data.
  • Program SDTM datasets and produce related CDISC deliverables such as aCRF, define.xml, reviewer’s guide, etc.
  • With minimal supervision, performs stakeholder management, negotiating timelines and scope of deliverables.
  • Participate in standards governance and developing biometric department operational processes.

Requirements

  • Bachelor’s or Master’s degree in a data science field, e.g., statistics, mathematics, epidemiology, computer science, bioinformatics, or another field with commensurate levels of experience.
  • Minimum 4+ years of biotechnology or pharmaceutical experience, with (immuno-) oncology experience preferred.
  • Good programming experience in SAS. Experience working with other languages (R) in validated environments is a plus.
  • Good knowledge of CDISC data standards (CDASH, SDTM).
  • Good knowledge of data standards and demonstrated experience in the handling of non-CRF data including proven ability to work with diverse data types, such as biomarker, PK/PD, pharmacovigilance, etc.
  • Demonstrated ability to rapidly adapt to changing project and strategic requirements.
  • Takes a fit-for-purpose mindset to daily work as well as long-term vision.

Benefits

  • Competitive market-based salary.
  • Opportunity to participate in stock programs.
  • Performance-based bonus.
  • Comprehensive benefits package.

A.B

Arcus Biosciences

Arcus Biosciences is a biotechnology company focused on developing innovative cancer therapies, particularly in the field of oncology and immunotherapy. The company emphasizes a collaborative and cross-functional approach to clinical development, aiming to drive the design, planning, and implementation of clinical trials for investigational products. With a commitment to scientific excellence and regulatory compliance, Arcus Biosciences fosters an inclusive work environment that values diversity and equal opportunity for all employees.

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