Director, Regulatory Affairs
Confidential
Executive Director, Regulatory Affairs
About the Company
Innovative biotechnology (BioTech) company specializing in precision therapies for autoimmune & inflammatory diseases
Industry
Biotechnology
Type
Privately Held, VC-backed
Founded
2025
Employees
51-200
Specialties
- biotechnology
- pharmaceuticals
- drug development
- clinical development
- inflammatory diseases
- autoimmune diseases
- immune-mediated diseases
- immunology
- and precision therapies
About the Role
The Company is seeking an Executive Director for Regulatory Affairs to lead the global regulatory strategy and execution for its innovative therapeutic candidates. The successful candidate will be a seasoned professional with a minimum of 15 years' experience in regulatory affairs, including at least 5 years as a Global Regulatory Lead. The role involves direct and coordinated regulatory strategy for a range of submissions, from INDs to marketing applications, and requires a deep understanding of global regulatory requirements, particularly in the US and Europe. The Executive Director will be responsible for maintaining compliance, managing regulatory timelines, and overseeing a team to ensure the accuracy and completeness of all regulatory documents. Experience in immunology is highly preferred, and the ideal candidate will have a proven track record of leading global marketing applications and post-marketing activities. Applicants for the Executive Director position at the company should hold an advanced degree in a relevant life sciences discipline and have a strong background in regulatory affairs within the pharmaceutical or biotechnology industry. The role demands a proactive, execution-oriented individual with excellent leadership, communication, and interpersonal skills. The candidate must be adept at managing and mentoring a team, as well as being able to work independently and collaboratively to drive the regulatory process. A successful candidate will be able to balance strategic oversight with hands-on execution, demonstrate an entrepreneurial mindset, and have a history of effective negotiations with global health authorities. The position is pivotal in the company's mission to develop and deliver precision therapies that have the potential to transform the lives of patients with autoimmune and inflammatory diseases.
Hiring Manager Title
Senior Vice President, Regulatory Affairs & Quality
Functions
- Legal
- Operations
$170.9k - $231.3k
OverviewThe Associate Director of Regulatory Affairs Strategy will serve as US Regional Lead or Global Regulatory Lead for our early/mid/late-stage CNS programs. The role will lead the regulatory strategy and facilitate submission of data packages to the US. The role is...SuggestedFull timeTemporary workLocal areaFlexible hours2 days per week$154.4k - $242.55k
...leads global strategies to maximize global regulatory success towards achievement of program... ....Accountabilities:The Associate Director will be responsible for complex or highly... ...understanding broad concepts within regulatory affairs and implications across the organization...SuggestedMinimum wageTemporary workLocal areaRemote work$170.9k - $231.3k
Overview The Associate Director, Regulatory Affairs CMC Development is responsible for developing and implementating global CMC regulatory strategies for development-stage programs. This role will play a critical part in shaping regulatory strategies for emerging therapeutic...SuggestedFull timeTemporary workWork at officeLocal areaFlexible hours$154.4k - $242.55k
...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$276k - $414k
Job Title: Executive 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 direction for first-in-class cell therapies...SuggestedHourly payFull timeTemporary workWork at officeWorldwideFlexible hours3 days per week$238k - $374k
...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 regulatory...Minimum wageTemporary workWork at officeLocal areaRemote workWorldwide$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$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$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... ...in Chemistry, Biology, Pharmacy, Regulatory Affairs, Pharmaceutical Sciences, Engineering, or...Full timeSummer workRemote workFlexible hours2 days per week$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...$168k - $252k
...Job Description General Summary The Regulatory Strategy Associate Director will be responsible for overseeing the development of regional or global... ...This role requires advanced understanding of regulatory affairs frameworks in the US, Europe, or other international markets...Summer workRemote workFlexible hours2 days per week$200k - $240k
...Associate Director, Regulatory Affairs Operations At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with bespoke Fc biotherapeutics engineered to selectively...Work at officeLocal area$142.5k - $256.5k
...The Role The Associate Director, Global Regulatory Advertising and Promotion will be responsible for ensuring compliance with regulatory requirements... ...This role will serve as a key liaison between Regulatory Affairs, Legal, Medical, and Commercial teams to provide strategic...Work at officeWork from home$210.4k - $331.1k
Job DescriptionDepartment- Global Regulatory Affairs and Clinical Safety - Vaccine & Infectious DiseaseBrief Description of Position-The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy...Full timeFor contractorsLocal areaWorldwideFlexible hours$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- ...JOB TITLE: Executive Director, Global Regulatory Affairs DEPARTMENT: Regulatory Affairs REPORTS TO: Vice President, Regulatory Affairs / Sr. Vice President, Regulatory Affairs LOCATION: Boston, MA DATE PREPARED: March 27, 2026 JOB SUMMARY: The Executive Director, Global...
$281k - $344k
...patients – realizing a world where people with immune‑mediated diseases can live life fully. Job Summary The Executive Director, Regulatory Affairs will report to the Senior Vice President, Regulatory Affairs & Quality and serve as the Global Regulatory Lead to provide...For contractorsLocal areaFlexible hours2 days per week- ...evolving clinical‑stage pipeline. This individual will work closely with the CMC, Quality Assurance, Clinical Drug Supply, and Regulatory Affairs teams to ensure the successful planning, development, and delivery of CMC regulatory strategy across programs. The ideal...Flexible hours
- ...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...
- ...S&P Global Energy seeks an Associate Director, Regulatory Research Associates to lead evaluation of state utility regulation and market developments across the U.S. energy sector. You will shape datasets, build analytical frameworks, and deliver high-impact insights to...
$163.5k - $281.6k
...best to work that truly matters for patients, we invite you to join us. Responsibilities Develop and implement comprehensive global regulatory CMC strategies for assigned gene therapy programs, including IND/CTA, BLA/MAA, and post-approval submissions. Lead and manage the...Full timeFor contractorsWork at officeFlexible hours- ...Veeva Systems, Inc. in Boston, MA seeks a Mastery-level Regulatory Information Management leader focused on growing the Regulatory product market share. You will bridge complex regulatory requirements with modern software solutions and act as the ultimate authority on...
$117k - $171k
...environmental engineering projects, including performing senior‑level technical analysis and review; Develop environmental permitting and regulatory strategy for a variety of industrial and construction projects; Manage the preparation and submission of permits and compliance...Hourly payFull timeTemporary workFor contractorsWork experience placementFor subcontractorWork at officeLocal areaWorldwideFlexible hours$220k - $290k
...innovative combination therapy in the U.S. and are exploring regulatory pathways for Europe and Japan. We are continuing to... ...the Corporation’s short and long‑term plans. The Senior Director, Regulatory Affairs has foresight, is action oriented, a problem‑solver, is a...Temporary workFor contractorsWork at officeWeekday work$183.55k - $275.32k
...Director/Sr. Director, Regulatory Labeling Strategy, Advertising, and Promotion, Regulatory Who we are: At Agios, we are fueled by connections to transform... .... Director: 10+ years of experience in Regulatory Affairs within the biopharmaceutical industry. 7+ years experience...Temporary workLocal areaRemote workWork from homeFlexible hours3 days per week- ...Vertex Pharmaceuticals LLC is seeking a Director of Regulatory Affairs CMC in Boston. The role leads a Regulatory CMC team, shaping global strategies for small molecule programs and coordinating Health Authority interactions across development and commercialization. Hybrid...
- ...Agios Pharmaceuticals seeks a Director/Sr. Director for Regulatory Labeling Strategy to provide strategic regulatory guidance. You will oversee labeling... ...possesses significant experience in regulatory affairs and will contribute to innovative medicine development....Remote work
$210.4k - $331.1k
...Job Description Regulatory Affairs Headquarters Principal Scientist is responsible for the development and implementation of global regulatory strategy for their assigned projects in the Vaccines and Infectious Disease therapeutic area. Responsibilities Serve as the single...For contractorsWorldwide- ...’s research and development is focused on understanding and meeting patient needs using our novel therapies. Tasks The Director of Regulatory Affairs provides strategic and operational leadership to the development and commercialization of products for one or more of the...
- ...Beeline Medicines is seeking an Executive Director, Regulatory Affairs to lead global regulatory strategy for multiple programs. The role oversees IND/CTA/NDA/MAA submissions, health authority interactions, and lifecycle management. Hybrid work with on-site days is expected...
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