Sr. Manager, Information Technology

Scorpion Therapeutics; South San Francisco (CA); Hybrid; USD 140,000 - 180,000; Full time

Job summary

Acadia seeks a leader to manage and strategically develop our Veeva-based commercial and medical platforms, including Vault CRM, MedComms, and PromoMats. The role partners with stakeholders to translate business needs into technical solutions and oversee platform lifecycle.

You will guide enhancements, integrations, and environment management while ensuring compliance within a regulated GxP setting. Domestic and international travel may be required.

Qualifications

• Bachelor's in Information Systems or related field required.
• 7+ years of Veeva platform administration experience in pharma/biotech.
• Veeva certifications preferred; strong knowledge of regulated GxP settings.

Responsibilities

• Act as primary technology partner translating business needs into technical solutions.
• Oversee platform lifecycle, enhancements, integrations and environment management.
• Manage vendor relationships and ensure compliance within a GxP environment.
• Document processes and maintain system governance.

Skills

Veeva administration

Stakeholder management

Project execution

GxP compliance

Veeva certifications

Education

Bachelor's in Information Systems or related field

Job description

Role: Lead the management and strategic development of Acadia's Veeva-based commercial and medical platforms, including Vault CRM, MedComms, and PromoMats.

Responsibilities: act as the primary technology partner for stakeholders, translating business needs into technical solutions, overseeing platform lifecycle, managing vendor relationships, and ensuring compliance within a GxP environment. Responsibilities include platform administration, system enhancements, integrations, environment management, and process documentation.

Requirements

• Bachelor's in Information Systems or related field, 7+ years of Veeva platform administration experience within pharma/biotech, Veeva certifications, and strong knowledge of regulated GxP settings.

Preferred skills include stakeholder management, project execution, and proficiency in technical and analytical tools.

High-Value: focus on commercial and medical Veeva ecosystems, cross-functional collaboration, and supporting compliance in regulated environments.

Location: hybrid work in San Diego or San Francisco, CA, with domestic and international travel as needed.