Manager, Regulatory Affairs
$100k - $143kRelay Therapeutics
We are looking for a motivated and strategic regulatory professional to join our growing regulatory team at Relay Tx. You will contribute to the development and execution of innovative regulatory strategies to support the advancement of our transformative pipeline. You will support the global regulatory lead to drive regulatory planning and execution for our development programs. You will collaborate with cross-functional teams to deliver domestic and international regulatory submissions including IND, CTA, NDA and MAA submissions. Your Role: You will work closely with research and development colleagues to support the development and execution of innovative regulatory strategies for programs ranging from first-in-human through late-stage clinical development, including the implementation of non-clinical and clinical regulatory strategy. You will coordinate the preparation and submission of high quality domestic and global regulatory submission documents (e.g. IND, CTA, NDA/MAA), ensuring compliance with applicable regulations and internal standards. You will assist in the preparation and conduct of meetings with health authorities, which includes the development of robust briefing packages and comprehensive meeting preparation to support successful outcomes of meetings. You will monitor for and integrate regulatory intelligence/guidelines into program strategies and contribute to risk identification and mitigation planning within development teams. You will support the efforts to plan and obtain regulatory designations including but not limited to breakthrough therapy designations, fast‑track designations, and orphan drug designations and contribute to the CDx strategy development and submissions. You will provide oversight to the global regulatory activities that are performed by our Clinical Research Organization (CROs) and regulatory vendors. Your Background: You have earned your B.S and/or M.S. and bring 2+ years of relevant experience. Advanced degree or education in a scientific field is a plus. You are results-oriented and have working knowledge of the drug development process and regulatory submissions (IND, CTA, NDA/MAA, etc.). Experience in precision oncology, rare disease and/or companion diagnostic (CDx) is a plus. You are a proactive problem-solver, capable of identifying solutions to regulatory challenges. You have strong verbal and written communication skills, including the ability to present strategic regulatory topics to internal teams. You are detail-oriented, organized, and able to work both independently and collaboratively in a fast-paced environment. You are intellectually curious and eager to contribute to a growing team focused on innovation and patient impact. Estimated Salary Range : [ $100,000 - $143,000 ]. The range provided above is based on what we believe to be a reasonable estimate for this job at the time of posting. Actual base salary will depend on a number of factors, including but not limited to, a candidate’s education, experience, skills and location. About Relay Therapeutics Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. We have built a world‑class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process. Our team is equal partsfearlessandrelentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you’re excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us! As set forth in Relay Therapeutics’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law. #J-18808-Ljbffr
$120k - $140k
...and preparation of document packages for regulatory submissions ensuring compliance with the... ....Participates in assigned Regulatory Affairs initiatives aimed at improving internal... ...required with the ability to successfully manage projects to deadlines. A working knowledge...SuggestedWork at office- ...Reference26-00886 Job Description: This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices... ...will contribute: With some supervision, plans, executes and manages regulatory submissions according to the regulatory strategy...Suggested
$145k - $215k
...inclusivity, so that our people are valued, seen, and heard.How you’ll make an impact:Kymera Therapeutics is seeking a Senior Manager, Regulatory Affairs to serve as a key regulatory contributor and emerging strategic leader across multiple drug development programs....Suggested$115k - $135k
...recognition. That’s who thrives at Arbor. If this resonates, read on. About the Role Arbor Biotechnologies is seeking a Manager, Regulatory Affairs, to support an expanding portfolio of gene editing programs. Reporting to the Director of Regulatory Affairs, this...Suggested- ...Senior Regulatory Affairs Manager- REMOTE I'm looking for a senior manager, regulatory affairs to lead our growing, dynamic team through global phase 3 clinical trials of a certain product and support other clinical studies. This role includes driving global submission...SuggestedFull timeRemote work
- ...operational leadership supporting global regulatory submissions from planning through... ...business lead for Regulatory Information Management and Veeva RIM Basics Partner with cross-... ...automation Partner closely with Regulatory Affairs, Medical Writing, Clinical Development,...
$168k - $252k
Job DescriptionGeneral Summary:The Regulatory Strategy Associate Director will be responsible... ...advanced understanding of regulatory affairs frameworks in the US, Europe, or other international... ...cross-functional teams and senior management on regulatory risks, considerations, and...Full timeSummer workRemote workFlexible hours2 days per week$154.4k - $242.55k
...leads global strategies to maximize global regulatory success towards achievement of program... ....Ensures project team colleagues, line management, and key stakeholders are apprised of developments... ...broad concepts within regulatory affairs and implications across the organization...Minimum wageTemporary workLocal areaRemote work- ...Compliance and Title VI Coordinator is responsible for oversight of the University’s compliance with Title VI, as well as overall case management of Title IX Hearings, Appellate Panels, NDAB Determination Panels, and matters subject to the University Committee on Rights and...Work at officeLocal area
$170.9k - $231.3k
Overview The Associate Director, Regulatory Affairs CMC Development is responsible for developing and implementating global CMC regulatory... ...along with strong communication, collaboration, and project management skills. This individual will play an important role in evaluating...Full timeTemporary workWork at officeLocal areaFlexible hours$154.4k - $242.55k
...therapies to patients worldwide.This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices... ...:With minimal supervision, develops, plans, executes and manages regulatory submissions per the GRA CMC Product Team technical...Minimum wageTemporary workLocal areaRemote workWorldwide$170.9k - $231.3k
OverviewThe Associate Director of Regulatory Affairs Strategy will work on assigned programs with the respective Global Regulatory Portfolio... ...Work with the Global Regulatory Lead and Regulatory Affairs management to lead and define regulatory strategy and to compile and...Full timeTemporary workLocal areaWorldwideFlexible hours2 days per week$268.2k - $402.2k
...DescriptionGeneral Summary:The Executive Director, Regulatory Strategy will serve as a seasoned... ...the T1D portfolio. This position will manage a group of global/regional regulatory... ...management on status of global Regulatory Affairs strategies and tactics, procedures and...Full timeSummer workLocal areaRemote workFlexible hours2 days per week$90k - $200k
...Senior Manager, Financial Investigations Kroll's North American Investigations, Diligence and Compliance practice is seeking a Senior... ...a broad range of complex investigations, forensic accounting, regulatory compliance, including business intelligence, internal (client)...Temporary workFlexible hours$150k - $215k
...Capital Overview With approximately $225 billion of assets under management, Bain Capital is one of the world's leading private investment... ...and Broader Responsibilities Coordinate management of regulatory inquiries and examinations; lead or support examination...Full time$110k - $160k
Compliance Manager Position, $110,000 - $160,000, discretionary annual bonusSenior professionals with 10+ years may command higher compensation... ...strategies. This role serves as a critical bridge between regulatory requirements and business operations in a dynamic asset...Work at officeLocal areaVisa sponsorship$238k - $374k
...therapies to patients worldwide.As Executive Director, Global Regulatory Affairs CMC Devices and Drug-Device Combination Product, you will... ...to align evidence generation, usability/human factors, risk management, and value messaging to regulatory and access requirements for...Minimum wageTemporary workWork at officeLocal areaRemote workWorldwide$238k - $374k
...best of my knowledge.Job DescriptionExecutive Director, Global Regulatory Affairs CMC Early DevelopmentAre you looking for a patient-focused... ..., modeling/simulation, predictive tools, data and knowledge management, and digital CMC dossiers) to strengthen scientific...Minimum wageTemporary workLocal areaRemote work$231.9k - $365k
Job DescriptionOur Regulatory Affairs team in General Medicine advances medical innovation to patients by establishing clear, timely, and robust... ..., and labeling, to ensure accuracy and consistency.Lead, manage, and review the performance of direct reports, including oversight...Full timeFor contractorsLocal areaWorldwideFlexible hours$190.4k - $285.6k
...Chemistry Manufacturing Controls (CMC) leads a Regulatory CMC team responsible for developing and... ..., data traceability, and knowledge management.Ensures programs are appropriately... ...Chemistry, Biology, Pharmacy, Regulatory Affairs, Pharmaceutical Sciences, Engineering, or...Full timeSummer workRemote workFlexible hours2 days per week$180k - $245k
...Therapeutics is seeking an experienced and strategic Director of Regulatory Affairs to lead and support global regulatory efforts across our... ...from early development through approval and lifecycle management.Ensure regulatory strategies align with corporate goals and...$116k - $160k
...dependent care. Job DescriptionWe are seeking an experienced regulatory professional to support global regulatory activities... ...late-stage development programs through lifecycle management. The Manager, Regulatory Affairs will partner cross-functionally to support high-...Flexible hours$215k - $235k
...like you then please read on!About the Role: The Director of Regulatory Affairs is responsible for leading regulatory strategy and execution... ...cross functional data narratives to support designation requests.Manage submission, agency correspondence, and follow up related to...- ...OfficerPosition SummaryThis individual will lead regulatory strategy and execution for growing... ..., and help build Regulatory Affairs capabilities as the clinical pipeline grows... ...changes, and clinical trial expansion. Manage external regulatory consultants and vendors...2 days per week3 days per week
- ...Dental Solutions team This role develops regulatory strategies for existing, new, and... ...and other (regulated) products This role manages and submits 510ks for the products and manages... ...activities for less senior Regulatory Affairs professionals, including but not limited...Work at office
- ...about AbbVie, please visit us at Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Senior Manager, Regulatory Affairs US & Canada Strategy Lead - Therapeutic Neurotoxins is responsible for the development and implementation of US and...Local area
$232k - $348k
Job DescriptionThe Regulatory Strategy Senior Director is a regulatory leader with expert technical and tactical experience... ...and GRA leadership. Counsels and advises senior management on status of global Regulatory Affairs strategies and tactics, procedures and...Full timeSummer workWork at officeLocal areaRemote workFlexible hours2 days per week3 days per week$196.7k - $353.4k
...seeking an individual to lead development and execution of global regulatory strategy for programs in its oncology portfolio. This leader... ...external to the company Demonstrated competence in employee management and development Knowledge of and broad experience with regulatory...Permanent employmentFull timeWork at officeWork from home- Job DescriptionGeneral Summary:The Regulatory Labeling Director will lead the strategic development... ...the strategic development and lifecycle management of labeling for that/those area(s),... ...10 years of experience in regulatory affairs in the area of global labeling or related...Full timeSummer workWork at officeLocal areaRemote workFlexible hours2 days per week
- ...compliance program to ensure adherence to legal, regulatory, and internal policies. The Compliance... .... The VP will work closely with senior management and various departments to proactively... ..., risk management, or regulatory affairs, with a strong understanding of industry...Local area
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