Product Manager

Paradromics, Inc. • Austin, TX

2d • Onsite

About The Position

Brain-computer interfaces have the power to turn incurable brain conditions into solvable engineering problems. At Paradromics, we're leading in the hardware that makes that possible — and we're now looking for someone to help us build the clinical and commercial communication infrastructure that will carry our platform from Early Feasibility Study through approval and beyond. We are looking for a Product Manager to sit within our Marketing team and serve as the connective tissue between our clinical, regulatory, and commercial functions. The immediate and most critical focus of this role is supporting our Early Feasibility Study (EFS) — developing the materials, strategies, and site-level tools that drive enrollment, enable clinical teams, and build the foundation for a successful path to market. We need someone who speaks both marketing and medtech fluently — and can bridge a fast-moving marketing team to the clinical and regulatory experts who drive our program. If you know how implantable devices actually get approved — and how to communicate that process to patients, clinicians, and regulators in language that lands — this role was built for you.

Requirements

• 4–7 years of experience in medical device or pharmaceutical marketing, medical communications, or a related field
• Experience with implantable devices is essential; background in neurology, neurosurgery, or neurotechnology strongly preferred
• Experience supporting clinical trial communications, patient recruitment marketing, or early feasibility/IDE-stage programs is required — this is the core of the role
• Demonstrated experience developing and executing direct-to-patient and HCP outreach strategies, ideally in a rare disease or specialty device context
• Deep familiarity with FDA promotional guidelines for devices and a track record of making sound, independent compliance judgments on marketing content
• Ability to translate dense clinical and scientific content into clear, compelling language for varied audiences — patients, clinicians, and regulators
• Proven experience working cross-functionally with Clinical Affairs, Regulatory Affairs, and Medical Affairs teams
• Comfort in clinical and surgical environments, including the ability to be present at implantation cases and patient home visits with professionalism and sensitivity
• Strong project management skills with the ability to manage multiple content workstreams, outreach campaigns, and review cycles simultaneously
• Collaborative instincts around content capture — comfortable being on-site for milestone moments and contributing to how those stories are shaped, without needing to lead production
• Bachelor's degree required; background in life sciences, communications, or health sciences preferred
• Willingness to travel approximately 20–30% of the time

Nice To Haves

• Experience navigating MLR or promotional review committees
• Knowledge of health literacy best practices and plain-language writing standards
• Familiarity with ALS, rare neurological disease, or disability advocacy communities
• Experience with patient advocacy partnerships or community-based outreach

Responsibilities

• Serve as the marketing point of contact for Connect-One study investigators, representing patient recruitment and media efforts at investigator meetings and internal team reviews
• Own the development of patient recruitment materials and strategies, including site-facing toolkits that help investigators identify and engage eligible patients
• Build and execute a national multi-channel HCP outreach strategy, working with surgeons and clinical partners to reach neurologists, neurosurgeons, and referring physicians across geographies
• Develop and execute direct-to-patient outreach in partnership with ALS organizations, patient advocacy groups, caregiver networks, and community events
• Develop patient-facing educational content explaining BCI technology, the trial process, and what participants can expect before, during, and after implantation — written to appropriate health literacy standards
• Partner with Clinical Affairs to support patient home visits, helping assess communication style and environment to inform how materials and messaging are tailored for individual participants
• Partner with Clinical Affairs and Regulatory Affairs to develop informed consent materials that are accurate, compliant, and accessible
• Create and maintain site and investigator-facing materials including procedure guides, clinical staff training resources, and reference tools for neurosurgeons, neurologists, and clinical coordinators
• Support the development of lay summaries and patient-facing components of IRB and FDA submission materials
• Manage the MLR review process for all EFS-related communications and ensure materials meet FDA promotional guidelines
• Be present on-site for landmark Paradromics moments — including first surgeries and early clinical activations.
• Ensure all outward-facing content — including press releases and website updates related to regulated products — complies with FDA promotional regulations, exercising sound independent judgment and escalating to Regulatory Affairs when in doubt
• Provide direct field support at clinical sites, including attendance at implantation cases and hands-on engagement with surgical and clinical teams
• Attend and represent the company at medical congresses, industry trade shows, and training functions
• Collaborate with Regulatory Affairs to develop consistent product labeling, indications for use language, and patient-facing IFUs
• Serve as the ongoing marketing liaison to Regulatory Affairs, making routine compliance calls on content and routing decisions independently while maintaining a conservative, escalation-first posture on ambiguous cases
• Support post-market surveillance by working cross-functionally to investigate product complaints and resolve quality issues
• Serve as the primary Marketing liaison to Clinical Affairs and Regulatory Affairs teams, bringing deep device industry fluency to a fast-moving marketing organization
• Maintain a library of approved language, data references, and content assets that the broader team can draw from with confidence
• Support go-to-market planning as the program advances from EFS toward pivotal trial and commercialization
• Adhere to all compliance, quality, and regulatory procedures governing the development and distribution of marketing materials

Benefits

• We will not win on marketing spend. We will win on the quality of our ideas, the credibility of our science, and the strength of the clinical foundation we build right now. If you want to be part of writing that story from the inside, we'd like to meet you.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 11-50 employees