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# Chief Medical Officer – Boston, MA


Role Overview for Chief Medical Officer – Boston, MA
JRG Partners is proud to lead the exclusive search for a visionary and strategic Chief Medical Officer (CMO) on behalf of our client, a rapidly growing and well-funded medical device company based in the heart of Boston’s thriving life sciences ecosystem. This is a pivotal executive leadership position for an individual passionate about revolutionizing patient care through groundbreaking technology. Our client is at the forefront of developing next-generation medical devices designed to address significant unmet needs in the healthcare landscape.
The Chief Medical Officer will be the senior clinical leader within the organization, reporting directly to the Chief Executive Officer and serving as a key member of the executive team. This individual will be responsible for defining and executing the company’s global clinical development and medical affairs strategy. The CMO will provide the medical and scientific vision that guides the company from early-stage clinical trials through to successful product commercialization and post-market surveillance.
You will be the primary voice of medical and clinical expertise, both internally to guide our cross-functional teams and externally to engage with regulatory bodies, key opinion leaders (KOLs), and the broader medical community. This role requires a unique blend of scientific rigor, strategic business acumen, and inspirational leadership to steer the company’s innovative portfolio towards global success and, most importantly, to make a tangible impact on patients’ lives.
Key Responsibilities of Chief Medical Officer – Boston, MA
The CMO will have a broad range of responsibilities, encompassing the entire clinical lifecycle of the company’s products. This is a hands-on, strategic role that demands both high-level oversight and deep involvement in tactical execution.
Clinical Strategy and Development

Develop and implement comprehensive, long-range clinical development plans that are aligned with corporate objectives and designed for successful global regulatory approvals and market adoption.
Provide direct oversight for the design, execution, and interpretation of all clinical studies, from early feasibility and pivotal trials to post-market registries and real-world evidence generation.
Author and review key clinical documents, including study protocols, investigator brochures, clinical study reports (CSRs), and regulatory submission sections (e.g., Clinical Evaluation Reports).
Ensure all clinical trials are conducted in strict adherence to Good Clinical Practice (GCP), ICH guidelines, and other applicable global regulations, prioritizing patient safety above all else.
Lead the biostatistics and data management functions, ensuring robust data collection, rigorous analysis, and clear interpretation of clinical trial results.
Develop and execute a high-impact publication and presentation strategy to disseminate clinical data in top-tier peer-reviewed journals and at major medical congresses.

Medical Affairs and Scientific Communication

Serve as the company’s lead medical expert, providing deep clinical and scientific insights across the organization, including to the R&D, marketing, and business development teams.
Establish and cultivate strong, collaborative relationships with a global network of Key Opinion Leaders (KOLs), clinical investigators, and scientific advisors.
Oversee the development of all medical and scientific communications, ensuring accuracy, consistency, and compliance in all materials, including medical information responses, MSL resources, and promotional materials.
Lead the company’s presence at scientific conferences, representing the organization and presenting key clinical data to the medical community.

Regulatory Affairs and Compliance

Provide critical clinical leadership and strategic input for all regulatory interactions and submissions with global health authorities, including the FDA’s Center for Devices and Radiological Health (CDRH), European Notified Bodies (under MDR), and other international agencies.
Play a leading role in meetings with regulatory bodies, articulating the clinical rationale and benefit-risk profile of the company’s products.
Collaborate closely with the Quality and Regulatory departments to ensure that all clinical activities are inspection-ready and that the company maintains a culture of compliance.

Safety and Risk Management

Establish and oversee a robust pharmacovigilance and medical device safety monitoring program for all products, both investigational and commercialized.
Lead the company’s Safety Review Committee, responsible for the ongoing evaluation of the benefit-risk profile of the product portfolio.
Develop and implement comprehensive Risk Management Plans in accordance with ISO 14971 and other global standards.

Executive Leadership

Build, mentor, and lead a world-class clinical and medical affairs organization, attracting and retaining top talent.
As a member of the executive team, contribute to the overall corporate strategy, long-range planning, and fundraising activities.
Provide clinical due diligence and expert assessment for potential M&A, licensing, and partnership opportunities.
Foster a dynamic, collaborative, and scientifically driven culture throughout the organization.

Requirements for the Chief Medical Officer – Boston, MA
We are seeking a seasoned and accomplished physician-executive with a proven track record of success in the medical device industry.
Required Qualifications & Experience
Medical Doctor (MD) or equivalent medical degree is required.

Board certification in a relevant medical specialty is highly preferred.
A minimum of 15 years of progressive experience in clinical research and development within the medical device, pharmaceutical, or biotechnology industry.
A minimum of 10 years in a leadership capacity, with demonstrated experience building and managing high-performing clinical development and/or medical affairs teams.
Extensive, hands-on experience designing and executing clinical trials for medical devices, particularly Class II and/or Class III devices.
A proven track record of successful regulatory submissions and interactions with the FDA (e.g., IDE, PMA, 510(k)) and other major international regulatory bodies.
Deep understanding of the global regulatory landscape, including GCP, ISO 14155, and medical device regulations (e.g., FDA 21 CFR 812, EU MDR).

Preferred Qualifications & Skills

An advanced degree such as a PhD, MPH, or MBA is a significant plus.
Experience in a small, fast-paced, entrepreneurial company environment is highly desirable.
Established network of relationships with KOLs and clinical investigators in a relevant therapeutic area.
Exceptional strategic thinking capabilities with the ability to integrate clinical, scientific, and commercial objectives.
Outstanding communication skills (written, verbal, and presentation) with the ability to articulate complex scientific concepts to a wide range of audiences, from board members to clinical site staff.
Strong leadership presence, with a demonstrated ability to inspire teams, influence stakeholders, and drive results in a collaborative, cross-functional setting.
Unquestionable personal integrity and a deep commitment to patient safety and ethical conduct.

Benefits & Perks Offered
Our client offers a highly competitive executive compensation and benefits package designed to attract and retain a leader of this caliber. The package includes:

Highly competitive base salary commensurate with experience.
Substantial annual performance-based bonus.
Significant equity stake in the company (stock options or RSUs) providing meaningful upside potential.
Comprehensive health, dental, and vision insurance plans for you and your dependents with low employee premiums.
A 401(k) retirement plan with a generous company matching contribution.
Generous paid time off (PTO) and company holiday schedule.
Full relocation assistance package for candidates moving to the Boston area.
Annual budget for professional development, including attendance at major medical conferences, continuing medical education (CME), and leadership training.
Access to executive coaching and leadership development programs.
A dynamic, innovative, and mission-driven work culture in a state-of-the-art facility.

How to Apply
JRG Partners has been exclusively retained for this critical executive search. If you are a visionary clinical leader with the experience and passion to drive the next wave of medical device innovation, we encourage you to apply.
To express your interest in this opportunity, please submit your curriculum vitae and a cover letter detailing your qualifications. All inquiries and applications will be handled with the strictest confidence. To learn more about our dedicated recruitment services in this space, we invite you to explore our expertise in Life Sciences executive search. We look forward to connecting with you.