Clinical Applications Manager

Cynosure, LLC•Westford, MA

18h

About The Position

The Clinical Applications Manager plays a leading role in the successful execution of global clinical trials and the generation of high-quality evidence to support the safety, effectiveness, and market adoption of Cynosure Lutronic technologies. This position combines hands-on field leadership with strategic involvement in shaping clinical programs that inform product development and innovation. The ideal candidate is an experienced clinician with a proactive, hands-on approach to site management, a strategic mindset capable of translating field experiences into actionable insights, and a passion for energy-based devices and elevating standards of care in Dermatology and Medical Aesthetics.

Requirements

Bachelor’s degree in nursing. Advanced degree (PA, MS, NP, or equivalent) preferred.
8+ years of clinical experience, in energy-based treatment delivery / clinical research.
Proven expertise and deep understanding of energy-based devices, developing clinical workflows, or executing clinical trials.
Deep familiarity with clinical-study design, working with IRB, data analysis, regulatory compliance, and publications.
Track record of engaging and influencing key opinion leaders and senior stakeholders.
Solid understanding of laser-tissue interaction and clinical workflows in Dermatology and Medical Aesthetics.
Strong foundation in clinical study design, trial operations, and data management practices.
Excellent verbal and written communication skills; able to translate complex information clearly across audiences.
Strategic thinker with a problem-solving mindset and a focus on actionable results.
High attention to detail with proven ability to manage multiple priorities across concurrent projects.
Proactive, self-directed, and adaptable in both independent fieldwork and cross-functional team environments.

Responsibilities

Responsible for delivering hands-on patient treatments and end-to-end management of the Westford in-house clinic.
Serve as primary contact for clinical sites, ensuring smooth trial implementation, patient enrollment, protocol adherence, and on-time delivery.
Manage day-to-day trial operations across multiple studies, ensuring timelines, objectives, and budgets are met.
Oversee preparation and delivery of study materials, clinical supplies, and investigational devices.
Monitor site performance and compliance with study protocols, GCP, and local regulatory requirements.
Maintain accurate tracking and management of study documentation, including data, consents, and compliance records.
Analyze and summarize clinical data to support internal reports, publications, and regulatory filings.
Partner with R&D, Marketing, and regional clinical teams to develop and execute a clinical roadmap aligned with innovation strategy and unmet needs.
Shape and refine clinical protocols and endpoints to support evidence generation and regulatory success.
Provide field-based clinical insights to inform product design, user workflows, and commercial messaging.
Support claims development and regulatory submissions with credible clinical input.
Stay informed on emerging trends, treatment practices, and standards of care in Dermatology and Aesthetics to guide forward-looking clinical programs.