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Medical Process Consultant

Hiring from
Europe, United States
Work type
Remote
Posted
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Engagement

  • Remote: EU or US East Coast

  • Duration: November–March

  • Allocation: Approximately 2–2.5 days/week

  • Total: Approximately 42 days

We are looking for an experienced Medical Process Consultant to support a global pharmaceutical transformation to Vault CRM. The consultant will translate Medical Affairs and Medical Information stakeholder needs into clear processes, controlled workflows, and testable business requirements.

Key Responsibilities

  • Lead medical process analysis and engage with MSLs, Medical Information teams, and global/local process owners.

  • Facilitate stakeholder sessions and reconcile regional requirements and variations.

  • Map medical engagement, medical insights, and inquiry workflows, including exceptions, handoffs, ownership, and closure criteria.

  • Develop process narratives, requirements, business rules, and acceptance scenarios.

  • Support the transition to Vault CRM by reviewing capabilities, identifying gaps, and documenting dependencies.

  • Review solution demonstrations, clarify requirements, and coordinate with Veeva and retained-system owners.

  • Support business testing and prepare handover documentation.

  • Identify and escalate policy, clinical, or safety-related decisions to the appropriate stakeholders.

Requirements

  • 5+ years of experience in business analysis or process consulting.

  • 3+ years of experience in pharmaceutical Medical Affairs, Medical Information, or medical CRM workflows.

  • 2+ years of relevant experience with Salesforce-based Veeva CRM processes.

  • Experience participating in at least one Vault CRM discovery, transition, requirements, configuration review, or business-testing project related to medical processes.

  • Experience working across multiple markets and directly with medical stakeholders.

  • Strong experience with SOP-based process analysis, requirements traceability, and acceptance criteria.

  • Understanding of scientific interaction recording, medical insights, inquiry routing, and the separation between medical and commercial activities.

  • Experience with medical information systems, safety escalation handoffs, or business UAT is a plus.

  • BPMN, Jira/Confluence, and German or French are desirable.

  • Life sciences, pharmacy, or related education is a plus but not required.

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