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Veeva Jobs in Summit, NJ (NOW HIRING)

ImmunityBio, Inc.

Veeva RIM Specialist

Summit, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position Summary The Veeva RIM Specialist will provide expertise and guidance in the management and publishing of regulatory documents ensuring their conformance with Health Authority requirements.

NKW NantKwest Inc

Veeva RIM Specialist

Summit, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position Summary The Veeva RIM Specialist will provide expertise and guidance in the management and publishing of regulatory documents ensuring their conformance with Health Authority requirements.

Teachercool

Veeva Quality Lead

Jersey City, NJ · On-site

... the Veeva Vault QMS framework, covering change control, deviation management, CAPA, audit management, document control, training compliance and supplier qualification ● Guide internal teams and ...

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Veeva information

What is a Veeva?

A Veeva job typically refers to a role involving Veeva Systems' software, which is used primarily in the life sciences industry for CRM, content management, and regulatory compliance. Professionals in Veeva roles may work as administrators, developers, consultants, or business analysts, focusing on implementing, configuring, or managing Veeva applications like Veeva Vault or Veeva CRM. These roles often require expertise in cloud-based software, data management, and industry-specific regulations.

What are the key skills and qualifications needed to thrive in a Veeva position?

To thrive in a Veeva Specialist or Consultant role, you need a strong understanding of Veeva Vault or Veeva CRM platforms, combined with expertise in life sciences business processes and data management. Familiarity with software configuration, data migration, and certifications like Veeva Vault Administrator or Veeva CRM certification are often required. Excellent problem-solving abilities, communication skills, and the capacity to collaborate effectively with cross-functional teams distinguish top performers in this position. These competencies are critical for supporting efficient system implementations, ensuring compliance, and driving user adoption in regulated industries.

What does a Veeva specialist or consultant do?

As a Veeva Specialist or Consultant, your daily responsibilities may include configuring Veeva Vault or Veeva CRM systems, managing user access, supporting system integrations, and responding to end-user support requests. You'll work closely with business stakeholders to gather requirements, troubleshoot issues, and ensure the software aligns with regulatory requirements in the life sciences sector. Additionally, you might collaborate with project managers, IT, and compliance teams to support new releases or process improvements. This role often requires balancing technical tasks with user training and ongoing documentation.

What job categories do people searching Veeva jobs in Summit, NJ look for?

The top searched job categories for Veeva jobs in Summit, NJ are:

What cities near Summit, NJ are hiring for Veeva jobs?

Cities near Summit, NJ with the most Veeva job openings:

Veeva jobs near you
Infographic showing various Veeva job openings in Summit, NJ as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 67% In-person, and 33% Remote job distribution.

Veeva RIM Consultant

Stark Pharma Solutions Inc

Piscataway, NJ • On-site

Contractor

Posted 17 days ago

Job description

Position: Veeva RIM Consultant
Location: Remote
Duration: Long Term

Job Overview

We are seeking an experienced Veeva RIM Consultant to support regulatory data remediation and Veeva RIM initiatives for a leading pharmaceutical client. The ideal candidate will have strong expertise in Veeva RIM, regulatory information management, and data quality, along with experience supporting digital transformation and automation initiatives within a regulated life sciences environment.

Key Responsibilities

  • Perform regulatory data remediation activities within Veeva RIM.
  • Configure, maintain, and support Veeva RIM applications.
  • Support regulatory information management processes and system enhancements.
  • Collaborate with cross-functional teams to improve regulatory data quality and compliance.
  • Assist with Veeva RIM reporting, dashboards, and KPI development.
  • Support integrations between Veeva Quality and Veeva RIM.
  • Participate in SDLC activities, including requirements gathering, testing, and deployment.
  • Contribute to AI and automation initiatives to streamline regulatory processes.
  • Ensure compliance with regulatory standards and documentation requirements.

Required Qualifications

  • Strong hands-on experience with Veeva RIM (Required).
  • Experience performing regulatory data remediation.
  • Knowledge of IDMP and Pharmacovigilance Management System (PMS) (Required).
  • Experience with eCTD submissions and regulatory publishing.
  • Understanding of Software Development Life Cycle (SDLC).
  • Experience with AI and process automation initiatives.
  • Knowledge of integrations between Veeva Quality and Veeva RIM.
  • Experience creating and analyzing Veeva RIM reports and KPIs.
  • Experience working in a regulated pharmaceutical or biotechnology environment.
  • Excellent analytical, communication, and cross-functional collaboration skills.