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Medical Process Consultant

其他限定地区(需当地身份)
公司TransPerfect
薪资未公开
工作地点United States
地域资格限定地区(需当地身份)
时区要求日间重叠约 9 小时,基本正常作息
用工类型Contractor
发布时间5 天前
数据来源Himalayas
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注意地域限制:该职位明确限定在 United States 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。

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.

Originally posted on Himalayas

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