ImmunityBio

Veeva Clinical Analyst

ImmunityBio$87K — $98K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in IT, Computer Science, Bio-Informatics, Life Sciences, or related field.
  • 2+ years of experience in IT support, data coordination, or application management role.
  • Prior exposure to clinical trial software systems is preferred.
  • Foundational knowledge or academic exposure to cloud systems, particularly Veeva Vault applications is a plus.
  • Familiarity with Excel and basic configurations in Veeva Vaults.

Responsibilities

  • Manage user administration for Clinical Vault applications.
  • Assist with system configuration, including modifying workflows and document types.
  • Create reports based on user requirements.
  • Act as first line of support for user access issues and clarify system behavior.
  • Draft documentation for Computer Software Validation and participate in User Acceptance Testing.
  • Support review and testing of Veeva software updates in sandbox environments.
  • Maintain data integrity and assist with data uploads and clean-up.

Benefits

  • Eligibility for a discretionary bonus and equity award.
  • Flexible work schedule available with manager approval.
  • Traditional working hours Monday to Friday.
  • Opportunities for cross-functional projects.
Full Job Description
Position Summary

Veeva Clinical Vault Systems Analyst provides foundational technical and operational support for ImmunityBio's cloud-based Veeva Clinical Vault applications. Working under manager guidance, this role assists in basic system configuration, user access management, and routine troubleshooting. This is an excellent opportunity for someone with a baseline understanding of life sciences software to develop specialized skills in a highly regulated GxP environment.

Essential Functions
  • Manage day-to-day user administration, including provisioning user accounts, assigning security profiles, and managing permission sets across Clinical Vault applications.
  • Assist in executing low-to-medium complexity system configurations, such as modifying picklists, updating document types, and adjusting basic lifecycle states or workflows.
  • Create basic reports and Dashboards based upon user provided requirements.
  • Monitor the access email inbox, acting as the first line of triage for end-user support. Diagnose access issues, clarify system behavior for users, and escalate complex technical bugs to senior team members or Veeva support.
  • Assist in drafting documentation for Computer Software Validation (CSV). Participate in executing User Acceptance Testing (UAT) scripts and documenting results in strict accordance with GxP and 21 CFR Part 11 regulations.
  • Support the review process for Veeva's routine software updates. Assist in testing new platform features in sandbox environments before they are pushed to production.
  • Maintain data integrity within the Vault by running routine reports, identifying data entry inconsistencies, and assisting with bulk data uploads or clean-up tasks.
  • Create, edit and adhere to Standard Operating Procedures (SOPs), process improvements, and standardization of templates.
  • Performs ad-hoc and cross-functional duties and/or projects as assigned to support business needs and provide developmental opportunities.


Education & Experience

  • Bachelor's degree in Information Technology, Computer Science, Bio-Informatics, Life Sciences, or a related field is required.
  • 2+ years of experience in an IT support, data coordination, or application management role is required.
  • Prior exposure to software systems used in clinical trials, pharmaceutical manufacturing, or regulatory affairs is highly preferred.


Knowledge, Skills, & Abilities

  • Foundational knowledge or academic exposure to cloud systems. Direct experience using or configuring Veeva Vault applications (such as eTMF, CTMS, CDMS/EDC or RIM) is a major plus but not strictly mandatory if the candidate has strong technical aptitude.
  • Understanding GxP validation meaning and a willingness to learn the rigorous documentation standards required in the life sciences industry.
  • Familiarity with Excel (for data mapping). Hands-on working knowledge of basic configurations, Veeva security, document types and reports in any of the Veeva vaults.
  • Understanding of DIA Reference model, Submissions structures, EDC development principles, Software Development Life Cycle.
  • Good communication skills and ability to collaborate with all levels of an organization.
  • Ability to adapt quickly, work independently and manage competing priorities.
  • Strong attention to detail.
  • Strong research & analysis skills, creative thinker who can focus on the details without losing sight of the big picture.


Working Environment / Physical Environment

  • This position works on site based in Dunkirk, NY.
  • Regular work schedule is Monday - Friday, within standard business hours. Flexibility is available with manager approval.
  • Must possess mobility to work in a standard office setting and to use standard office equipment, including a computer.
  • Lift and carry materials weighing up to 20 pounds


This position is eligible for a discretionary bonus and equity award. The hourly base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.

$42.20 (entry-level qualifications) to $47.12 (highly experienced) per hour

The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.

ImmunityBio uses artificial intelligence (AI) tools to assist with sourcing and identifying potential candidates for open positions. These tools help us reach qualified applicants and improve the efficiency of our recruitment outreach. No preference is given to applicants sourced or identified by AI tools.

Important: AI is not used to screen, evaluate, rank, assess, or make hiring decisions about applicants. All applications are reviewed by human recruiters and hiring managers. Hiring decisions are made solely by ImmunityBio personnel without automated decision-making.

About ImmunityBio

ImmunityBio is a biotechnology company that develops immunotherapies for cancer and infectious diseases. The company's lead product candidate is a cancer vaccine that targets multiple tumor antigens. ImmunityBio was founded in 2015 by Patrick Soon-Shiong, and has raised over $1 billion in funding from investors such as NantWorks and Blackstone Group.
Learn more about ImmunityBio
Size
200 employees
Market Cap
$2 billion
Industry
Net Income
-$92.3 million
5 Year Trend
+84.2%
Revenue
$110,000
NASDAQ

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