Veeva Safety Consultant-5 at Realign LLC
Illinois, Illinois, USA -
Full Time


Start Date

Immediate

Expiry Date

04 Dec, 25

Salary

0.0

Posted On

04 Sep, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Web Development, Computer Science, Management Skills, Validation, Life Sciences

Industry

Information Technology/IT

Description

JOB SUMMARY:

We are seeking a highly skilled Veeva Safety Consultant to join our team and support the implementation, optimization, and management of the Veeva Vault Safety Suite. This role will play a key part in ensuring regulatory compliance, data integrity, and process efficiency in pharmacovigilance operations. The ideal candidate has hands-on experience with Veeva Vault Safety, understands global drug safety regulations, and can bridge the gap between technical configuration and business requirements.

QUALIFICATIONS:

  • Bachelor’s or Master’s degree in Life Sciences, Computer Science, or related field.
  • 3+ years of experience in Veeva Vault Safety or similar pharmacovigilance systems.
  • Solid understanding of pharmacovigilance regulations and industry best practices.
  • Experience with system implementation, configuration, and validation (CSV).
  • Excellent communication and stakeholder management skills.
  • Ability to work independently in a fast-paced and dynamic environment.
  • Veeva certification (preferred but not required).

REQUIRED SKILLS

Graphic Design Consultant Web Development & Analytics Consultan

Responsibilities
  • Lead or support implementation and configuration of Veeva Vault Safety modules (e.g., Safety, SafetyDocs, MedDRA integration).
  • Collaborate with pharmacovigilance and IT teams to gather requirements and translate them into functional system specifications.
  • Provide subject matter expertise on drug safety workflows, case intake, processing, reporting, and safety data exchange.
  • Configure system workflows, user roles, security profiles, and custom objects within the Veeva Safety ecosystem.
  • Ensure compliance with global regulatory standards (e.g., FDA, EMA, ICH) and support audit readiness.
  • Assist with validation activities including IQ/OQ/PQ, documentation, and testing efforts.
  • Conduct user training, support change management, and act as a liaison between business and technical teams.
  • Troubleshoot system issues, coordinate with Veeva support, and implement solutions for system enhancements.
  • Stay updated with Veeva product releases and recommend improvements or new features.
Loading...