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Senior Clinical Database Programmer
Senior Clinical Database ProgrammerActalent • South San Francisco, California, USA
Senior Clinical Database Programmer

Senior Clinical Database Programmer

Actalent • South San Francisco, California, USA
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  • [job_card.full_time]
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Job Title : Sn Clinical Database Programmer

Job Description

We are seeking a Sn Clinical Database Programmer to provide expertise in clinical database programming. This role is crucial in ensuring that clinical programming deliverables are completed on time, within budget, and adhere to quality standards and study requirements. You will play a key role in leading clinical data build and management activities for multiple trials, ensuring the success of both outsourced and in-house projects.

Responsibilities

  • Lead and oversee Electronic Data Capture (EDC) build, migration, post-production management, and deployment.
  • Develop and execute user acceptance testing plans and test scripts.
  • Implement data integrations with external vendor data sources such as IRT, laboratory, and imaging.
  • Oversee setup of other clinical management systems like IRT and JReview.
  • Contribute to the preparation of clinical data programming documents.
  • Manage URL configuration and access.
  • Lead the development of custom and Business Objective reports, SAS clinical programming report specifications, and data visualization output.
  • Standardize and develop Standard Operation Procedures and work instructions.
  • Collaborate with Clinical Science, Clinical Operations, Data Management, and Safety teams to create specifications and develop reports and tools.

Essential Skills

  • Bachelor's degree in computer science, health-related field, or a related discipline.
  • 6-8 years of experience in clinical programming or relevant work experience.
  • 5+ years of programming experience.
  • 2+ years of experience working with Veeva CDMS clinical software solutions.
  • Experience in the life sciences industry and clinical trial processes.
  • Strong knowledge of CDISC standards, FDA and ICH / GCP regulations and guidelines.
  • Additional Skills & Qualifications

  • CRO or CDM vendor management experience in oncology.
  • Early phase adaptive trial management experience preferred.
  • Experience with CDASH terminology.
  • Experience with R or SAS programming techniques is a plus.
  • Experience with Rave is a plus.
  • Experience with Spotfire and / or JReview is a plus.
  • Proficient in configuration, design, testing, validation, data collection, data review process, and data standardization.
  • Work Environment

    This is a fully remote position requiring availability during West Coast hours. You will work in a dynamic and multidisciplinary team environment, collaborating both internally and externally.

    Job Type & Location

    This is a Contract position based out of South San Francisco, CA.

    Pay and Benefits

    The pay range for this position is $70.00 - $105.00 / hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following :

  • Medical, dental & vision
  • Critical Illness, Accident, and Hospital
  • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
  • Life Insurance (Voluntary Life & AD&D for the employee and dependents)
  • Short and long-term disability
  • Health Spending Account (HSA)
  • Transportation benefits
  • Employee Assistance Program
  • Time Off / Leave (PTO, Vacation or Sick Leave)
  • Workplace Type

    This is a fully remote position.

    Application Deadline

    This position is anticipated to close on Jan 28, 2026.

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