Executive Director, Regulatory Affairs CMC
$290k - $323kCrescent Biopharma, Inc.
Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies as single agents and as part of combination regimens to treat a range of solid tumors. For more information, visit and follow the Company on LinkedIn and X. Responsibilities Lead and/or oversee global regulatory CMC submissions (e.g., INDs, CTAs, BLAs, MAAs etc.) through product lifecycle. Proactively identify regulatory risks, opportunities, and mitigation strategies in alignment with objectives, and communicate to management, as needed Provide strategic regulatory guidance to TechOps and Quality organizations to ensure global compliance and readiness for clinical and commercial supply Serve as the primary interface with global regulatory agencies for CMC-related negotiations, milestone meetings, and information requests. Provides global regulatory input and support on product-compliance related activities including change controls, deviations, and investigations. Manage junior team members and contractors to support development activities Education & Experience BS/BA Degree in a Scientific Discipline, Advanced Degree (M.S., Ph.D., etc.) required 12 years’ experience in Regulatory Affairs CMC in Pharma/Biotech Strong negotiation skills with health authorities (e.g.FDA, EMA) as well as submissions Experience with leading IND and Marketing Applications Experience with antibody drug conjugates and biologics Strong analytical, strategic thinking, and problem-solving skills. Excellent communication and leadership abilities; able to influence across all levels of the organization. Ability to thrive in a fast-paced, ambiguous environment while managing competing priorities. Commitment to fostering a diverse and inclusive workplace What We Offer Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environment Competitive compensation, including base salary, performance bonus, and equity 100% employer-paid benefits package Flexible PTO; also, two, one-week company-wide shutdowns each year A commitment to your professional development, with access to resources, mentorship, and growth opportunities Salary Range The salary range for this position is $290,000 to $323,000. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Additional Description for Pay Transparency: The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation – Unlimited PTO; Sick time – 10 days per calendar year; Holiday pay, including two Company shut downs; Parental Leave – 16 weeks within one year of the birth/adoption/foster care of a child; FMLA; Military Leave. Additional information can be found - Please note: Crescent Biopharma is an Equal Opportunity Employer. We are committed to fostering a diverse, inclusive, and equitable workplace where all individuals are valued and respected. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, sexual orientation, national origin, disability, veteran status, or any other protected status. #J-18808-Ljbffr Crescent Biopharma, Inc.
$290k - $323k
...LinkedIn and X. Responsibilities Lead and/or oversee global regulatory CMC submissions (e.g., INDs, CTAs, BLAs, MAAs etc.) through product... ...S., Ph.D., etc.) required 12 years’ experience in Regulatory Affairs CMC in Pharma/Biotech Strong negotiation skills with health...SuggestedTemporary workFor contractorsFlexible hours$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 Early Development you will provide strategic leadership and development to global CMC regulatory subject...SuggestedFull timeTemporary workLocal areaWorldwide$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...SuggestedMinimum wageFull timeTemporary workWork at officeLocal areaRemote workWorldwide$207k - $253k
...MASH). This role provides strategic, tactical and operational regulatory CMC leadership to support clinical trial applications, market... ...projects. Key Responsibilities Independently develop and lead execution of regulatory CMC investigational, registration and/or post‑approval...SuggestedFull timeFlexible hours$207k - $253k
## Director, Regulatory Affairs CMCApplylocations: MA - Waltham - Officetime type: Full timeposted on:... ...tactical and operational regulatory CMC leadership to support clinical trial... ...*** Independently develops and leads execution of regulatory CMC investigational, registration...SuggestedMinimum wageFull timeLocal areaFlexible hours- ...pipeline. This individual will work closely with the CMC, Quality Assurance, Clinical Drug Supply, and Regulatory Affairs teams to ensure the successful planning,... ...candidate brings deep expertise in CMC regulatory execution for mid- to late-stage clinical development,...Flexible hours
$250k - $310k
...LinkedIn and Facebook. Location: Waltham, MA Role Summary The Executive Director, Regulatory Affairs serves as a visionary leader who shapes long-term... ...international regulations related to clinical, nonclinical, and CMC development is critical Deep industry knowledge Ability...Local area$190.4k - $285.6k
...Director, Regulatory Affairs CMCSkip to main content#Director, Regulatory Affairs CMC page is loaded## Director, Regulatory Affairs CMCApplylocations: Boston, MAtime type:... ...Regulatory CMC team responsible for developing and executing global regulatory strategies across...Summer workRemote workFlexible hours2 days per week$196k - $240k
...functional improvement for individuals, families and communities. Role Summary The Director, Regulatory Affairs – Chemistry, Manufacturing, and Controls (CMC) is responsible for defining and executing global CMC regulatory strategies for Dyne programs across all stages of...Local areaWorldwide$170k - $230k
Associate Director, Regulatory Affairs CMC Waltham, MA Skyhawk Therapeutics is seeking a hands‑on Associate Director, Regulatory Affairs CMC (RegCMC) to support the development and execution of the global RegCMC strategy for Skyhawk's small molecule pipeline. Working closely...$159k - $195k
...Facebook. Department 1310US - Regulatory - US Location Waltham, MA... ...Summary The Associate Director, Regulatory Chemistry Manufacturing and Control (CMC) is accountable for executing global CMC regulatory strategies... ...Serves as the Regulatory Affairs CMC representative in...Local area- ...Job Title: Executive Director, Global Regulatory Affairs Department: Regulatory Affairs Reports To: Vice President, Regulatory Affairs / Sr. Vice President... ...closely with Clinical Development, Clinical Operations, CMC/Technical Operations, Nonclinical, Biometrics, Medical...
$170.9k - $231.3k
## Associate Director, Regulatory Affairs, CMCUnited StatesApply NowFind out how well you match with this... ...Director, Regulatory Affairs CMC Development is responsible for developing... ...Responsibilities*** Lead the development and execution of global CMC regulatory strategies...Full timeTemporary workWork at officeLocal areaFlexible hours$204k - $245k
...we approach every challenge with radical care. The Director, Regulatory CMC is responsible for leading execution of global CMC regulatory strategies for approved... ...experience, with relevant experience in CMC regulatory affairs for biologics or gene therapy products Experience...Full timeWork at officeFlexible hours3 days per week$182k - $275k
...Opportunity Overview This role is responsible for executing high-quality, science-based, and compliant regulatory CMC deliverables for assigned program(s), in... ...with strategies established by Global Regulatory Affairs and Technical Operations. This individual contributor...Work at office$270k - $350k
The Senior Director, Regulatory Affairs is responsible for planning, developing, and implementing regulatory... ...of clinical, nonclinical, and CMC regulatory strategy—including preparation... ...Demonstrated success developing and executing regulatory strategy for small...Shift work- ...provide durable, life‑changing impact. Led by an established executive team and backed by world‑class life science investors,... ...diseases can live fully. Job Summary The Executive Director, Regulatory Affairs will report to the Senior Vice President, Regulatory Affairs...For contractorsLocal area2 days per week
- ...Vice President, Chemistry, Manufacturing, and Controls (CMC) About Kernal Biologics, Inc. Kernal Bio is a venture-backed... ..., potency assessment, and release testing. Define and execute the CMC regulatory strategy, including authoring IND and CTA sections and...Contract workFlexible hours
$212k - $333.19k
...therapies to patients worldwide. About the role As Senior Director and Regulatory Platform Lead GRA CMC, Device and Drug‑Device Combinations Human Factors,... ...effective strategies are implemented and project execution is on target Evaluate new business development opportunities...Full timeTemporary workLocal areaWorldwideNight shift- ...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...
$189k - $246k
...Department: 107000 Regulatory Location: San Diego, USA- Remote Position Summary The Director, Regulatory Affairs Strategy is responsible for developing and executing global regulatory strategies for Phase... ...Medical Affairs, Biostatistics, CMC, Quality, Nonclinical,...Temporary workLocal areaRemote workWeekend work- ...Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Senior Manager Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients to deliver biologics...Work at officeLocal areaRemote work
$170k - $220k
Associate Director, Regulatory CMC - Solid Biosciences Charlestown, MA HQ Solid Biosciences is a precision... ...CMC and quality teams, including execution of change management and data... ...4 years of experience in regulatory affairs in the pharmaceutical/biotech, including...Full timeTemporary workRemote workFlexible hours- ...Hemab seeks a Director, Regulatory Affairs who will be responsible for developing and executing innovative global regulatory strategies for the global development of candidates... ...yourself. You bring expertise in global CMC regulatory requirements and approach challenges...Work at office
$245k - $300k
...Biosciences is seeking an experienced and strategic Senior Director, Regulatory Affairs to lead and execute global regulatory strategies across our development... ...Operations, Biostatistics, Pharmacovigilance, CMC, Nonclinical, Quality, and Executive Leadership to advance...Local area- ...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...
- ...pain neurosciences inflammation metabolic disease infection fibrosis respiratory diseases drug-discovery cmc ind enabling and drug development Business Classifications B2B Enterprise About the Role The Company...
$293k - $358k
...the strategic direction and operational execution of Remix’s most advanced program that integrates clinical, regulatory, CMC, medical affairs, and commercial functions into one... ...Executive Leadership Team (ELT) and Board of Directors; develop and present program updates...- ...GlaxoSmithKline in the United States seeks a Senior Director, Global Regulatory Strategy – Oncology to lead regulatory strategies for asset development and lifecycle plans. The role collaborates with Early Development, Clinical, Safety, and Commercial teams to shape submissions...
$272k - $340k
...Program Management is accountable for the operational execution of Kailera’s development programs, with a strong emphasis... ...across the portfolio Partner closely with Clinical, Regulatory, CMC, and Medical Affairs to ensure Phase3 plans are fully integrated and execution...Contract workFor contractorsWork at officeLocal areaFlexible hours3 days per week
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