高级产品经理 - 生命科学会议管理(欧洲/美国 - 远程)
Senior Product Manager - Life Sciences Meetings Management (Europe/US - Remote)
使命 - 我们存在的意义、我们的工作以及为何需要你
SpotMe 是一家领先的 B2B 事件平台,帮助企业在线下、线上、混合模式活动和网络研讨会中通过与 CRM 连接的高质量体验提升活动影响力。我们专注于生命科学领域,SpotMe 支持 Onomi:Live HCP Engagement Platform,使医疗和商业团队能够高效地举办大会、专题会议、顾问委员会和网络研讨会。SpotMe 和 Onomi 共同将现场活动转变为公司最有效的参与渠道。
制药公司使用活动平台作为注册表单,而请求、审批、预算、HCP 注册、价值转移(ToV)和报告则在 Excel 中或通过代理完成。我们正在构建 Onomi 360,这是一款生命科学战略会议管理(SMM)产品,用于取代该领域的现有活动平台。首批客户已经在 Onomi 360 中运行他们的会议请求和审批;需求已得到验证,发展轨迹令人兴奋。
你的重点将是 MeetingsEQ,Onomi 360 的 SMM 层:一个统一的入口,用于每项请求、审批和预算配置,统一的 HCP 身份,按参会者分配 ToV,以及将参与和支出流回 CRM 而无需重新输入。客户的 CRM 和主数据保持原样;会议项目背后的活动平台是我们发挥作用的地方。AI 辅助开发是我们的工作方式,你将有真正的自由去使用它。
这个职位适合一位来自生命科学会议、合规或 HCP 数据领域的实干型产品经理,他们更倾向于交付和测试而不是讨论问题,并希望从头到尾负责一个产品,看到他们曾经操作的流程被现代的、以 AI 为先的工作流所取代。
作为 Onomi 360 高级产品经理,你将向产品副总裁汇报。你的时间将用于:
- [35%] 定义详细的产品。将客户工作簿、操作规程、RFP 要求和我们的能力图谱转化为路线图优先级和可构建的规格。
- [30%] 交付。每天与 Onomi 360 代码库中的设计和工程团队合作:精简的生产切片、原型、范围讨论、在运行产品中的验证。日常的基于 AI 的原型设计和客户验证。
- [25%] 客户和合作伙伴。与会议运营、合规、医学事务、财务、代理机构和客户的数据团队合作。定义 Onomi 360 如何与 Veeva、Salesforce、Snowflake 等系统集成。
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Mission - Why we exist, what we do, and why we need you
SpotMe is a leading B2B event platform that helps enterprises increase the impact of their events by delivering CRM-connected, high-quality experiences across in-person, virtual, hybrid events, and webinars. With a strong focus on life sciences, SpotMe powers Onomi: the Live HCP Engagement Platform that enables medical and commercial teams to run impactful congresses, symposia, advisory boards, and webinars. Together, SpotMe and Onomi turn live events into a company’s most effective engagement channel.
Pharma companies use event platforms as registration forms while request, approval, budget, HCP registration, transfer of value (ToV), and reporting run in Excel and at agencies. We are building Onomi 360, the life-sciences strategic meetings management (SMM) product, to replace the incumbent event platform in that space. First accounts already run their meeting requests and approvals in Onomi 360; the demand is validated and the trajectory is exciting.
Your focus will be MeetingsEQ, the SMM layer of Onomi 360: one front door for every request, approval and budget as configuration, unified HCP identity, per-attendee ToV allocation, and engagement and spend flowing back into the CRM without re-keying. The customer's CRM and master data stay where they are; the event platform behind the meetings program is where we play. AI-assisted development is how we work, and you will have real freedom to use it.
This position is the ideal role for a hands-on product leader from the life-sciences meetings, compliance, or HCP-data world who would rather ship and test than talk about the problem, and who wants to own one product end to end and see the process they once operated replaced with a modern, AI-first workflow.
As a Senior Product Manager, Onomi 360, you will be reporting to the VP Product. Your time will be spent on:
- [35%] Defining the detailed product. Turn customer workbooks, operating procedures, RFP requirements, and our capability map into roadmap priorities and build-ready specifications.
- [30%] Shipping. Work daily with design and engineering in the Onomi 360 codebase: thin production slices, prototypes, scope calls, validation in the running product. Daily AI-based prototyping and customer validation.
- [25%] Customers and partners. Work with meetings operations, compliance, medical affairs, finance, agencies, and the customer’s data team. Define how Onomi 360 works with Veeva, Salesforce, Snowflake, and consent, and own the venue-sourcing and fair-market-value partner integrations.
- [10%] Product truth. Keep what we claim, what we demo, and what we ship documented, clear and moving in the right direction.
Objectives - The problems you will solve
In your first month, you will:
- Take over the first customer’s move from their meeting request form to Onomi 360: spec, build, history migration, customer session.
- Get set up with AI-based toolkit and the Onomi 360 codebase, and use both in your daily work.
- Meet the early access customers (design partners) for Onomi 360.
After 3 months, you will have:
- The first customer live on meeting request and approvals in Onomi 360, measured against their baseline.
- The roadmap priorities for the next two quarters defined, and the first priorities specified to build depth with engineering.
- A clean separation everyone uses: aspirational (slides), forward-looking (prototype-based demo), and committed (roadmap and backlog).
After 6 months, you will have:
- The full end-to-end MeetingsEQ product specified and engineering-reviewed, request through approval, budget, HCP registration, ToV, and reporting.
- One customer replacing Excel with the Onomi 360 ToV module, and the first live account expanded from request and approval into budget, ToV, or venue sourcing.
After 12 months, you will have:
- One customer closing a full ToV reporting cycle in Onomi 360 instead of Excel.
- Three accounts running request to closure in production, and the org-wide calendar or HCP engagement view used outside compliance.
- Onomi 360 winning the meetings-management scope in RFPs.
What you need to be great at
- Life-sciences meetings, compliance, or transparency operations. You have built or operated workflows spanning approval, budgeting, ToV, and closure, and you know what EFPIA and Sunshine disclosure mean in practice.
- HCP data and integration fluency. Identity across Veeva, Salesforce, OneKey, and NPI; match rates; what a data team expects from a write-back.
- Domain-to-product translation. A messy operating process becomes states, rules, configuration, permissions, and audit events, with regulation separated from customer policy.
- Sequencing. The smallest production slice that proves the model without hiding the hard architectural or compliance question.
- Bias to execute. You ship, prototype, and put things in front of users in days, not spend weeks describing the problem. You drive decisions to a close and pull others along.
- Precise writing and direct communication. Specs detailed enough to build and review, plain words, disagreement in the open.
- Technical and AI fluency. You work in Claude Code or OpenAI Codex, you understand code, data flows, and architecture well enough to challenge an engineering design. You know the software development lifecycle deeply, from RFC and specification through review, release, and support. AI takes you from evidence to a testable artifact in hours.
What we want to hear about
- Life-sciences meetings and transfer of value. Tell us about a meetings or transfer-of-value process you built or ran end to end, from request through approval, budget, HCP registration, and disclosure. Where did it break, and what did you change? This is the process Onomi 360 replaces, and we want someone who has lived it.
- From operating process to product. Tell us about a messy process you turned into a product: which rules you made fixed, which you made configurable, what you integrated, and what you left manual. That translation is the heart of this role.
- Shipping fast. Tell us about the last thing you shipped or prototyped within two weeks of first hearing the problem. What did you skip, and what did users do with it? Here you put working software in front of pharma design partners every few weeks, not slides.
- Building with AI. Tell us about something you built yourself with Claude Code or another AI tool that changed a product decision, and what it taught you about the code or the architecture underneath. AI-assisted development is how we build, and you will have real freedom to use it.
Fluent English (written and spoken). Remote, based in Europe or in the US Eastern or Central time zones, with about 10-20 % travel to design partners and industry events.
SpotMe recruits, compensates, and promotes regardless of race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, parental status, or veteran status.
Originally posted on Himalayas