医学流程顾问
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
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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