Stealth Neurotechnology Company
VP of Clinical Science
San Francisco
Lead clinical science and scientific affairs for a Class III program, designing and executing the clinical evidence strategy required for a successful PMA. Build a strong scientific foundation through KOL engagement, publications, and medical education. This role requires a rigorous clinical scientist and strategic leader who can operate hands-on in a startup environment.
Key Responsibilities
- • Own the clinical evidence strategy in support of the Class III PMA pathway, including IDE strategy, pivotal trial design, endpoints, and statistical considerations.
- • Lead the development of clinical protocols, investigator brochures, clinical investigation plans, and related study documents.
- • Drive clinical data interpretation, evidence synthesis, and preparation of clinical sections for regulatory submissions.
- • Partner closely with Regulatory, Quality, and R&D to ensure clinical evidence aligns with design controls, risk management, and overall product strategy.
- • Lead scientific affairs strategy, including KOL identification, advisory board development, and long-term scientific partnerships.
- • Drive publication and congress strategy (abstracts, manuscripts, presentations) to build clinical awareness and scientific credibility.
- • Represent the company at key scientific and medical meetings; support medical education and training initiatives.
- • Serve as a scientific spokesperson with clinicians, investigators, and external stakeholders.
- • Provide clinical and scientific input to Board updates, investor materials, and due diligence processes.
- • Contribute to reimbursement and health economics strategy through clinical evidence planning.
Required
- • Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant scientific or clinical field;
- • Demonstrated success leading clinical strategy and evidence generation for at least one Class III PMA (or equivalent high-risk pathway).
- • Strong expertise in clinical trial design, endpoints, biostatistics interpretation, and GCP/FDA clinical regulations.
- • Proven ability to engage and manage KOLs, build advisory boards, and drive high-impact publications and scientific communications.
- • Experience operating in a startup or high-growth environment, with comfort being both strategic and hands-on.
- • Excellent written and verbal communication skills; ability to translate complex clinical science for diverse audiences (regulators, investors, clinicians, Board).
Preferred
- • Direct experience with IDE submissions, pivotal trial execution, and PMA clinical modules.
- • Background in complex devices (e.g., implants, interventional systems, or software-enabled technologies).
- • Prior leadership of a clinical or scientific affairs function in a Series A–C company.
- • Experience contributing to health economics/outcomes research or reimbursement strategy.
- • Existing network of relevant KOLs and investigators in the target therapeutic area.
Benefits & Perks
- • An opportunity to work on exciting, cutting-edge projects to transform patients’ lives in a highly collaborative work environment.
- • Competitive compensation, including stock options.
- • Comprehensive benefits package.
- • 401(k) program with matching contributions.
Company Overview
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.
Team Culture
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.
Job Description
We are seeking an experienced VP of Clinical Science 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.
Role Responsibilities
Required Qualifications
$260,000 - $320,000 USD
What We Offer
Echo Neurotechnologies is an Equal Opportunity Employer (EOE). We celebrate diversity and are committed to creating an inclusive environment for all employees.
Confidentiality
All applications will be treated confidentially. Applicants may be asked to sign an NDA after the initial stages of the interview process.
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.
Team Culture
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.
Job Description
We are seeking an experienced VP of Clinical Science 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.
Role Responsibilities
- Own the clinical evidence strategy in support of the Class III PMA pathway, including IDE strategy, pivotal trial design, endpoints, and statistical considerations.
- Lead the development of clinical protocols, investigator brochures, clinical investigation plans, and related study documents.
- Drive clinical data interpretation, evidence synthesis, and preparation of clinical sections for regulatory submissions.
- Partner closely with Regulatory, Quality, and R&D to ensure clinical evidence aligns with design controls, risk management, and overall product strategy.
- Lead scientific affairs strategy, including KOL identification, advisory board development, and long-term scientific partnerships.
- Drive publication and congress strategy (abstracts, manuscripts, presentations) to build clinical awareness and scientific credibility.
- Represent the company at key scientific and medical meetings; support medical education and training initiatives.
- Serve as a scientific spokesperson with clinicians, investigators, and external stakeholders.
- Provide clinical and scientific input to Board updates, investor materials, and due diligence processes.
- Contribute to reimbursement and health economics strategy through clinical evidence planning.
Required Qualifications
- Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant scientific or clinical field;
- Demonstrated success leading clinical strategy and evidence generation for at least one Class III PMA (or equivalent high-risk pathway).
- Strong expertise in clinical trial design, endpoints, biostatistics interpretation, and GCP/FDA clinical regulations.
- Proven ability to engage and manage KOLs, build advisory boards, and drive high-impact publications and scientific communications.
- Experience operating in a startup or high-growth environment, with comfort being both strategic and hands-on.
- Excellent written and verbal communication skills; ability to translate complex clinical science for diverse audiences (regulators, investors, clinicians, Board).
- Direct experience with IDE submissions, pivotal trial execution, and PMA clinical modules.
- Background in complex devices (e.g., implants, interventional systems, or software-enabled technologies).
- Prior leadership of a clinical or scientific affairs function in a Series A–C company.
- Experience contributing to health economics/outcomes research or reimbursement strategy.
- Existing network of relevant KOLs and investigators in the target therapeutic area.
$260,000 - $320,000 USD
What We Offer
- An opportunity to work on exciting, cutting-edge projects to transform patients’ lives in a highly collaborative work environment.
- Competitive compensation, including stock options.
- Comprehensive benefits package.
- 401(k) program with matching contributions.
Echo Neurotechnologies is an Equal Opportunity Employer (EOE). We celebrate diversity and are committed to creating an inclusive environment for all employees.
Confidentiality
All applications will be treated confidentially. Applicants may be asked to sign an NDA after the initial stages of the interview process.
Keep track of your job search
Save personal notes for each job to track your thoughts, application status, and follow-ups.
Try for freeUpload your resume
Sign up to upload your resume and get AI-powered customization for job applications.
Sign up freePractice your interview
Get AI-powered mock interviews tailored to this VP of Clinical Science San Francisco role. Upload your resume and practice with real-time voice feedback.
Sign up to practice