Associate Consultant, Entry-Level Clinical Data Technology Consulting

Veeva Systems

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Hybrid

Quick summary

Work type
Hybrid
Location
MadisonBoston, MANew York, NY
Posted
12 days ago
Freshness
Confirmed live today

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How this pay compares to similar roles

Similar $152k
$104k $189k
below market most similar roles pay here above market

This listing doesn't post a salary. Most similar roles pay $123,750–$180,500.

Based on 240 similar postings.

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About Veeva Systems

Veeva Systems is a cloud software company serving the global life sciences industry, providing CRM, clinical, regulatory, quality, and data applications used by pharmaceutical and biotech companies.

Veeva Systems currently has 72 open roles on FindRole.

Listed pay typically runs $80,000–$175,000 across 69 roles with salary data.

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At a glance

TL;DR · Associate Consultant, Entry-Level Clinical Data Technology Consulting

As an Associate Consultant - Entry-Level Clinical Data Technology Consulting within the Consultant Development Program, you will join the Professional Services team to support global Life Sciences companies. You will work hands-on with clinical data management technology to design, configure, and implement cloud and AI solutions. Your daily responsibilities include leading discovery workshops to gather requirements, tailoring the Vault CDMS platform to specific study protocols, and managing project scopes from design through go-live. You will utilize skills in data analysis, database concepts, and communication to solve complex clinical trial data management problems. The role requires familiarity with SQL, Python, or R, and a background in quantitative or life science fields to help optimize clinical data collection and study management processes for maximum long-term business value.

What you'll do

  • Design and configure the Vault CDMS platform to meet unique clinical trial requirements.
  • Structure clinical data models and set up study workflows based on study protocols.
  • Lead interactive discovery workshops with stakeholders to gather business requirements.
  • Translate customer visions into actionable technical specifications and data management workflows.
  • Scope study requirements and build timeline estimates for project deliverables.
  • Manage project milestones from initial study design through the final go-live.
  • Provide expert guidance on best practices to optimize clinical data collection processes.

What we're looking for

  • Candidates must be legally authorized to be employed in the United States.
  • Applicants must live within a reasonable commuting distance of the Madison, Boston, or New York offices.
  • Candidates must have a maximum of 2 years of postgraduate experience.
  • A Bachelor's or Master's degree in a quantitative or life science field is preferred.
  • Prior experience in healthcare data management, clinical trial operations, or technical consulting is highly valued (preferred).
  • Prior experience in data analysis using SAS, SPSS, Python, or R is highly valued (preferred).
  • Basic familiarity with database concepts such as SQL, Python, or R is required.
  • Work Authorization: Qualified candidates.

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