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VP of Clinical Science

ECHO RESTO OÜ
San Francisco · KohapealTäistööaegLisatud 1 näd tagasi

<div class="content-intro"><h2 data-pm-slice="1 1 []">Company Overview</h2> <p>Echo Neurotechnologies is an exciting new startup in the Brain-Computer Interface (BCI) space, driving innovation through advanced hardware engineering and AI solutions. Our mission is to deliver cutting-edge technologies that restore autonomy to people living with disabilities and improve their quality of life.</p> <p>&nbsp;</p> <h2>Team Culture</h2> <p>Join a small, dedicated team of knowledgeable and motivated professionals. Our early-stage environment offers the opportunity to take ownership of broad decisions with significant and long-lasting impact. We emphasize continuous learning and growth, fostering cross-functional collaboration where your contributions are vital to our success.</p></div><h3>Job Description</h3> <p>We are seeking an experienced <strong>VP of Clinical Science</strong> to lead clinical science and scientific affairs for our Class III program. This is a high-impact leadership role responsible for designing and executing the clinical evidence strategy required for a successful PMA, while building a strong scientific foundation through KOL engagement, publications, and medical education. The ideal candidate is both a rigorous clinical scientist and a strategic leader who can operate hands-on in a startup environment while preparing the organization for clinical trials and regulatory success.</p> <h3>Role Responsibilities</h3> <ul> <li>Own the clinical evidence strategy in support of the Class III PMA pathway, including IDE strategy, pivotal trial design, endpoints, and statistical considerations.</li> <li>Lead the development of clinical protocols, investigator brochures, clinical investigation plans, and related study documents.</li> <li>Drive clinical data interpretation, evidence synthesis, and preparation of clinical sections for regulatory submissions.</li> <li>Partner closely with Regulatory, Quality, and R&amp;D to ensure clinical evidence aligns with design controls, risk management, and overall product strategy.</li> <li>Lead scientific affairs strategy, including KOL identification, advisory board development, and long-term scientific partnerships.</li> <li>Drive publication and congress strategy (abstracts, manuscripts, presentations) to build clinical awareness and scientific credibility.</li> <li>Represent the company at key scientific and medical meetings; support medical education and training initiatives.</li> <li>Serve as a scientific spokesperson with clinicians, investigators, and external stakeholders.</li> <li>Provide clinical and scientific input to Board updates, investor materials, and due diligence processes.</li> <li>Contribute to reimbursement and health economics strategy through clinical evidence planning.</li> </ul> <h3>Qualifications</h3> <h4>Required Qualifications</h4> <ul> <li>Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant scientific or clinical field<s>;</s></li> <li>Demonstrated success leading clinical strategy and evidence generation for at least one Class III PMA (or equivalent high-risk pathway).</li> <li>Strong expertise in clinical trial design, endpoints, biostatistics interpretation, and GCP/FDA clinical regulations.</li> <li>Proven ability to engage and manage KOLs, build advisory boards, and drive high-impact publications and scientific communications.</li> <li>Experience operating in a startup or high-growth environment, with comfort being both strategic and hands-on.</li> <li>Excellent written and verbal communication skills; ability to translate complex clinical science for diverse audiences (regulators, investors, clinicians, Board).</li> </ul> <h4>Preferred Qualifications</h4> <ul> <li>Direct experience with IDE submissions, pivotal trial execution, and PMA clinical modules.</li> <li>Background in complex devices (e.g., implants, interventional systems, or software-enabled technologies).</li> <li>Prior leadership of a clinical or scientific affairs function in a Series A–C company.</li> <li>Experience contributing to health economics/outcomes research or reimbursement strategy.</li> <li>Existing network of relevant KOLs and investigators in the target therapeutic area.</li> </ul><div class="content-pay-transparency"><div class="pay-input"><div class="title">Salary</div><div class="pay-range"><span>$260,000</span><span class="divider">&mdash;</span><span>$320,000 USD</span></div></div></div><div class="content-conclusion"><h2 data-pm-slice="1 1 []">What We Offer</h2> <ul> <li> <p>An opportunity to work on exciting, cutting-edge projects to transform patients’ lives in a highly collaborative work environment.</p> </li> <li> <p>Competitive compensation, including stock options.</p> </li> <li> <p>Comprehensive benefits package.</p> </li> <li> <p>401(k) program with matching contributions.</p> </li> </ul> <p>&nbsp;</p> <h2>Equal Opportunity Employer</h2> <p>Echo Neurotechnologies is an Equal Opportunity Employer (EOE). We celebrate diversity and are committed to creating an inclusive environment for all employees.</p> <p>&nbsp;</p> <h2>Confidentiality</h2> <p>All applications will be treated confidentially. Applicants may be asked to sign an NDA after the initial stages of the interview process.</p></div>

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