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MAXconnect is a curated group of former payers, proxy payers, regulatory experts from around the globe who we call for counsel and ad-hoc advice

Join MAXconnect

Cutting edge projects
in Rare Disease / CGTs

‘Bring in an expert’
referral bonus​

Competitive and
punctual payments​

MAXconnect Payer Sign-Up

Please provide your email address for future contact

Please note, we will review your survey answers, add you to our MAXconnect database and contact you if your profile and experience fits a future project

Please provide your workplace address

This will help us to understand the relevant payers required for particular projects. We will not keep your details on file if you choose to opt out of joining MAXconnect, our internal expert database.
1Do you currently work for an organization or government body where a conflict of interest may arise if we were to call on your services as an advisor?
2Our interviews are conducted in English, please indicate your level of English proficiency
3Do you have prior experience or knowledge in the following? (tick all that apply)
4During the interviews we would require insights from a former/proxy HTA, pricing or regulatory perspective. What perspective / experience best describes you? (tick all that apply)
5At which level(s) can you provide payer and/or regulator perspectives? (tick all that apply)
6Please specify all countries / regions / regulatory bodies you can provide robust insights for
7Do you have prior experience or knowledge of the following therapeutic products? (tick all that apply)

P4A pay on a per use basis, typically by hour. The compensation rate can vary from each project and dependent on the fair market value rates set by our client.

We want experts who can advise on:

  • Macro and micro environmental insights
  • Future trends for price, access and procurement
  • Clinical trial design feedback; value story & messages
  • Advising on evidence gaps and mitigation strategies
  • Optimize an asset’s value communication
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We are award winning global experts in access for orphan drugs and Cell and Gene Therapies.

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