Director of Regulatory
$175k - $225kElucid
We are a rapidly growing, Boston-based medical technology company using AI to enable clinicians to make informed decisions on cardiovascular care - leading to better patient outcomes, improved quality of care, and reduced healthcare costs. Come work at Elucid and be part of delivering on our mission to prevent heart attacks and strokes!Every product we build has to earn its way to patient care, and regulatory strategy is how it gets there. We're looking for a Director of Regulatory who thrives on translating complex, evolving global requirements into clear paths to clearance for AI-enabled medical imaging software. You'll lead the execution of our regulatory strategy across FDA, EU MDR and other international markets, guiding submissions from pre-sub through post-market lifecycle management for a quickly growing startup. Partnering closely with our Quality, Engineering, Clinical, Commercial and Product teams, you'll sit at the center of how we bring innovative cardiovascular software safely and compliantly to the people who need it.The ideal candidate will have:7+ years of Regulatory Affairs experience in the medical device industry, with a track record of successful submissions in the US and EU (pre-submissions, IDEs, 510(k)s, De Novo, EU MDR product registrations).Advanced degree in Regulatory Affairs, Life Sciences, Engineering, or a software-related discipline.2-5+ years of people management experience, with strong cross-functional collaboration and communication skills.Expertise in global device regulatory requirements and standards (21 CFR Part 820, EU MDR, ISO 13485, ISO 14971, IEC 62304, IEC 62366). Experience in Software as a Medical Device (SaMD); familiarity with FDA Class II devices and EU MDR Class IIa/IIb products preferred.Strong collaboration and communication skills, with the ability to translate complex regulatory requirements into actionable guidance and drive effective, cross-functional execution.Work Location:This role is based out of our office in Boston, MA. For local candidates, we operate in a hybrid model with regular in-office collaboration. Candidates outside of the Boston area are invited to apply as fully-remote employees.Salary Range:The anticipated base salary range for this position at Elucid is $175,000-$225,000. Compensation will be influenced by a wide array of factors including but not limited to internal pay equity, job-related knowledge, skills, education, relevant experience, certifications, and geography as outlined in the job description.SummaryLocation: Boston, MA, United StatesType: Full TimeExperience: Senior Manager/Supervisor
$170.9k - $231.3k
OverviewThe Associate Director of Regulatory Affairs Strategy will work on assigned programs with the respective Global Regulatory Portfolio Lead, Global Regulatory Lead and cross-functional team to lead and define the regulatory strategy, facilitate submission of data...SuggestedFull timeTemporary workLocal areaWorldwideFlexible hours2 days per week$154.4k - $242.55k
...Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex... ...their regional counterparts.Accountabilities:The Associate Director will be responsible for complex or highly complex or multiple...SuggestedMinimum wageTemporary workLocal areaRemote work$154.4k - $242.55k
...the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of...SuggestedMinimum wageTemporary workLocal areaRemote workWorldwide$268.2k - $402.2k
Job DescriptionGeneral Summary:The Executive Director, Regulatory Strategy will serve as a seasoned regulatory leader with expert technical and tactical regulatory knowledge and advanced drug development expertise in Type 1 Diabetes (T1D). The incumbent will be responsible...SuggestedFull timeSummer workLocal areaRemote workFlexible hours2 days per week$170.9k - $231.3k
## Associate Director, Regulatory Affairs, CMCUnited StatesApply NowFind out how well you match with this jobJob ID3315This role is considered:Hybrid**Overview**The Associate Director, Regulatory Affairs CMC Development is responsible for developing and implementating...SuggestedFull timeTemporary workWork at officeLocal areaFlexible hours$238k - $374k
...that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionExecutive Director, Global Regulatory Affairs CMC Early DevelopmentAre you looking for a patient-focused company that will inspire you and support your career?...Minimum wageTemporary workLocal areaRemote work$238k - $374k
...we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.As Executive Director, Global Regulatory Affairs CMC Devices and Drug-Device Combination Product, you will provide strategic leadership and development to global...Minimum wageTemporary workWork at officeLocal areaRemote workWorldwide$190.4k - $285.6k
Job DescriptionGeneral Summary:The Director, Chemistry Manufacturing Controls (CMC) leads a Regulatory CMC team responsible for developing and executing global regulatory strategies across multiple investigational and commercial products in the small molecule portfolio....Full timeSummer workRemote workFlexible hours2 days per week$232k - $348k
Job DescriptionThe Regulatory Strategy Senior Director is a regulatory leader with expert technical and tactical experience in regulatory strategy for the assigned global or regional position and will be responsible for overseeing the development and implementation of advanced...Full timeSummer workWork at officeLocal areaRemote workFlexible hours2 days per week3 days per week$185.6k - $278.4k
Job DescriptionGeneral Summary:The Regulatory Labeling Director will lead the strategic development of global labeling on one or more marketed products. This role will be responsible for the development and maintenance of global product labeling across a therapeutic area...Full timeSummer workWork at officeLocal areaRemote workFlexible hours2 days per week$218.06k - $327.09k
Job Title: Senior Director, Regulatory Affairs Strategy - Cell Therapy Available locations: Gaithersburg, MDBoston, MASouth San Francisco, CASanta Monica, CAIntroduction to role: Are you ready to set the global regulatory vision for pioneering cell therapies and turn breakthrough...Hourly payFull timeTemporary workStart working todayWork at officeFlexible hours3 days per week$215k - $235k
...above self. At Arbor, our people embrace these qualities, so if this sounds like you then please read on!About the Role: The Director of Regulatory Affairs is responsible for leading regulatory strategy and execution for Abror’s development programs across the portfolio,...$180k - $245k
OverviewMonte Rosa Therapeutics is seeking an experienced and strategic Director of Regulatory Affairs to lead and support global regulatory efforts across our development programs, with a focus on immunology. The ideal candidate will be responsible for developing and...- ...comLocation: Watertown, MA - Hybrid, 2-3 days/week onsiteReports to: Chief Medical OfficerPosition SummaryThis individual will lead regulatory strategy and execution for growing clinical-stage oncology pipeline. The role will work closely with Clinical Development,...2 days per week3 days per week
$196.7k - $353.4k
The RoleModerna is seeking an individual to lead development and execution of global regulatory strategy for programs in its oncology portfolio. This leader will shape regulatory pathways for novel, first-in-class therapeutics and drive successful global development and...Permanent employmentFull timeWork at officeWork from home$196.7k - $353.4k
The Role:Moderna Therapeutics is seeking a Sr. Director of Regulatory Strategy to support oncology programs to be based in its Cambridge headquarters. This is a newly created role intended for a forward looking, creative regulatory strategist able to anticipate and address...Permanent employmentFull timeWork at officeWork from home$231.9k - $365k
Job DescriptionOur Regulatory Affairs team in General Medicine advances medical innovation to patients by establishing clear, timely, and... ...rigor and professionalism.Position Description:The Executive Director, Regulatory Affairs Liaison reports to the Vice President (VP)...Full timeFor contractorsLocal areaWorldwideFlexible hours- ...Cambridge, US; New Jersey, US | full time | Job ID: 9842 About the role: As an Associate Director in Regulatory Affairs, Advertising and Promotion at BioNTech, you will play a pivotal role in ensuring our promotional materials and medical communications comply with...Full timeWork at office
- ...Zugo-cel CAR-T franchise at CRISPR. Reporting to the Head of Regulatory Affairs, you will work closely with cross-functional teams and... ...demonstrated track record of significant accomplishments: ~ Associate Director: ~12+ Years of relevant experience with a bachelor's degree...Contract workRemote work
$166.4k - $249.6k
Job DescriptionGeneral Summary:The Chemistry Manufacturing Controls (CMC) Associate Director leads and executes global regulatory CMC strategies across investigational and commercial products focusing on biologics. This role is accountable for authoring, reviewing, and...Full timeSummer workRemote workFlexible hours2 days per week$143k - $233k
As part of the Pharmaceutical Development team, this position will play a key role in regulatory strategy development and execution of assigned Chemistry, Manufacturing and Control (CMC) programs. Your Role: With minimal supervision, accountable for developing and leading...$136.5k - $270k
...organizational success.Provide leadership and technical guidance on complex financial statement disclosures, accounting matters, and regulatory requirements, including the interpretation and application of GAAP and other relevant accounting standards.Serve as the senior...Temporary workWorldwideFlexible hours- About the OpportunityAn innovative neuropsychology company is seeking an experienced and strategic regulatory leader to join a growing biotechnology organization advancing innovative therapies for patients with significant unmet medical needs. This individual will play...
$195k - $330k
..., seen, and heard.How you’ll make an impact:Act as the global regulatory strategy lead for Kymera’s IRF5 degrader program, developing and... ...required; advanced degree preferred but not required.Director: 8-10 years of Regulatory Affairs experience. Senior Director:...Flexible hours$195k - $330k
...inclusivity, so that our people are valued, seen, and heard.How you’ll make an impact:Lead the development and execution of global regulatory CMC strategies for degrader programs across all stages of development, from early-stage activities through late-stage development...$182k - $275k
...overcome barriers, together.Opportunity OverviewThis role is responsible for executing high-quality, science-based, and compliant regulatory CMC deliverables for assigned program(s), in alignment with strategies established by Global Regulatory Affairs and Technical...Work at office$275k - $315k
Position OverviewBicara Therapeutics is seeking a strategic and experienced Senior Director of Regulatory Affairs to lead and execute US regulatory strategy for our biologics pipeline. Reporting to the VP, Regulatory Affairs, you will serve as the primary US regulatory...Full timeTemporary workWork at officeLocal area3 days per week$220k - $249.71k
...novel medicines. Most importantly, while experience within a Regulatory Writing department at a growing biotech is beneficial, a motivated... ...Affairs team at Entrada is a dynamic, growing team. The Director of Regulatory Writing will coordinate and lead the efficient generation...Work at office- ...Akebia Therapeutics in Cambridge, MA is seeking a Director of Regulatory Affairs - Labeling. This high-visibility role shapes global labeling strategy and partners cross-functionally to ensure labeling complies with FDA and global requirements. You will influence senior...Work at officeRelocation
- ...Bausch Health Companies Inc. is seeking a Senior Director of Advertising & Promotion – Regulatory Affairs to lead and participate in reviews of promotional labeling for prescription, OTC, and cosmetics in the US, with support for Canada. The role ensures materials comply...
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