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About Vita PanaceaVita Panacea is building Nexus- the first medication system you don’t have to hide.We’re creating a connected, design-led platform for people managing complex therapies at home- bringing structure, clarity and control to treatment that is currently fragmented and difficult to live with.The RoleThis is not a typical role.You will work directly with the founder to generate early traction from zero- speaking to patients, clinicians and partners, and shaping how this product comes to market.If you prefer structure and clear instructions, this isn’t the right fit.If you like figuring things out and building from scratch, it is.This role exists to build external credibility, validation, and access for Vita Panacea across:Clinical environmentsRegulatory pathwaysNHS and private healthcare systemsYour job is to turn early engagement into clear signals that de-risk the company for investors, partners, and regulators.You will act as the central point of coordination across clinical, regulatory, and external partners, ensuring progress is structured, visible, and aligned with company milestones.Clinical Validation & Market AccessDrive patient and clinician engagement into structured insight and validationBuild a pipeline of pilot opportunities (NHS and private sector)Secure letters of intent (LOIs) and early partnership signalsEstablish relationships across providers, clinics, and care networksPartnerships & External SignallingBuild and manage strategic partnerships (clinical, commercial, research)Convert activity into clear, usable proof pointsShape the validation narrative for investors and stakeholdersRegulatory & NHS NavigationWork closely with external regulatory partners to define and progress a clear regulatory pathwayCoordinate inputs required for MHRA classification, DTAC, DSPT, and broader compliance frameworksOwn day-to-day regulatory communication and follow-ups, ensuring timelines and outputs stay on trackTranslate regulatory requirements into clear internal actions and prioritiesManage NHS/ HIN/ stakeholder correspondence related to adoption and complianceResearch & Evidence PartnershipsEstablish academic and research collaborationsIdentify opportunities for formal validation or studiesContribute to a coherent evidence generation strategyWhat Success Looks LikeClear regulatory pathway defined and in motionActive NHS and private pilot pipeline and initiation3–5 LOIs or strong partnership signals securedEarly research and academic collaboration establishedA credible validation narrative strengthening fundraisingCompensationFractional consultancy role (flexible, outcome-driven)Monthly retainer in the range of £2,500–£3,000 depending on experienceTime commitment expected to vary depending on priorities and project phaseEquity available for long-term involvementHow to ApplySend a short note outlining:Relevant experienceExamples of partnerships, pilots, or validation work you’ve drivenWhy this role specifically
