Director, Regulatory Affairs CMC
$189.7k - $237.1kAcadia Pharmaceuticals
Position Summary Director, Regulatory CMC. Role can be based in San Diego, CA; San Francisco, CA; or Princeton, NJ. Hybrid model: work in office three days per week on average. Primary Responsibilities Manage CMC regulatory affairs for marketed products and compounds in development (US and ex-US). Coordinate with R&D, Pharmaceutical Development, Manufacturing, Quality, Regulatory, and other functions to develop/implement CMC regulatory strategy. Prepare high-quality CMC sections of INDs, CTAs, NDAs, MAAs, and amendments for worldwide submissions. Serve as CMC regulatory representative; primary point of contact with regulatory agencies for CMC development, registration, and lifecycle activities. Provide CMC regulatory guidance/strategy to development teams and identify/assess/mitigate regulatory risks. Ensure CMC compliance with applicable regulatory requirements. Evaluate manufacturing processes/changes for regulatory implications and support implementation. Maintain current knowledge of relevant guidelines/regulations and determine applicability. Education/Experience/Skills Bachelor’s degree in life science or related field (or equivalent education/experience). ~10 years progressively responsible CMC Regulatory Affairs experience in small molecule development; 5 years in a management role. Knowledge of global regulatory CMC requirements/guidelines. Experience preparing/submitting CMC components of IND/CTA filings; regulatory briefing packages; NDA and ex-US MAA submissions. Cross-functional collaboration; strong organization/detail; deadline management; initiative and ability to work with limited supervision. Ability to negotiate/influence senior leaders. Willingness and ability to travel domestically and internationally. Benefits/Compensation (as stated) Salary range: $189,700—$237,100 USD. Discretionary bonus and equity awards; medical/dental/vision; life/disability/travel/EAP; 401(k) match; ESPP; 15+ vacation; 13–15 paid holidays; sick time; paid parental leave; tuition assistance. #J-18808-Ljbffr Acadia Pharmaceuticals
$189.7k - $237.1k
...week on average. Position Summary Join Acadia as the Director, Regulatory CMC and play a critical role in advancing innovative small molecule... ...Primary Responsibilities Manages the CMC regulatory affairs activities for marketed products and compounds in development...SuggestedFull timeWork at officeLocal areaRemote workWorldwideShift workNight shiftDay shift3 days per week$212.5k - $250k
...Director For Regulatory CMC Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our "People first" approach means we also highly value...SuggestedFor contractorsLocal area- ...Job Description Job Description Our Pharmaceutical client is seeking a Director Regulatory Affairs Chemistry Manufacturing & Controls (CMC) to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development...SuggestedWork at office
- ...About Freyr Freyr is a global Regulatory Affairs and Life Sciences consulting organization supporting pharmaceutical, biotechnology, medical... ...Job Title: Sr Manager, Global Regulatory Affairs Strategist CMC Job Type: Permanent Job Location: Princeton NJ, - Remote...SuggestedPermanent employmentFull timeLocal areaRemote workFlexible hours
$145.6k - $279.4k
...the preparation, review, and submission of regulatory applications, including product... ...medical devices. Represents Regulatory Affairs on research, development, and marketing project... ...partnership with Clinical, Nonclinical, CMC, Analytical Development, Quality, Pharmacovigilance...SuggestedWork at officeRemote workRelocation packageFlexible hours- ...Director, Regulatory CMC Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases... ...a Director, Regulatory CMC as part of the Regulatory Affairs team based in Somerset, NJ. Key Responsibilities Develop...Worldwide
- ...Description Job Description Our Pharmaceutical client seeks a Global Director Regulatory Affairs Strategy to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development programs in collaboration with...
$127.31k - $167.1k
...innovative immunotherapies for patients living with multiple myeloma. Legend Biotech is seeking a Manager Regulatory CMC as part of the Regulatory Affairs team based in Somerset NJ. Role Overview This position will support the development and execution of...Permanent employmentFull timeTemporary workFor contractorsLocal areaWorldwideFlexible hours$200k - $300k
...We offer an opportunity for you to learn and grow while making significant contributions to the company's success. The Regulatory Affairs (Clinical/Nonclinical) role will drive regulatory strategy and execution within SI Project development teams and the RA Department...Full time$195.9k - $244.9k
...LinkedIn. Job Overview: This position reports to Executive Director, Regulatory Affairs and is part of the Biopharma R&D Regulatory Affairs... ...collaboration, and idea sharing Reviews nonclinical, clinical and CMC documentation (e.g. summary documents, nonclinical study...Full timeWork at officeLocal areaRemote workWorldwideFlexible hours$180k - $200k
...not presently approved by any regulatory authority other than Chinas... ...of Analytical Development and CMC Statistics will provide technical... ...MSAT Quality Regulatory Affairs Supply Chain and external CDMOs... ...legally protected status. Required Experience: Director...Full time$340k - $420k
...The VP/SVP, Head of Regulatory Affairs will provide strategic and operational leadership for the Company’s global regulatory function and serve... ...Clinical Development, Biostatistics, Clinical Operations, CMC, and other functions to optimize development and registration...Full time$168.37k - $220.99k
...advance innovative immunotherapies for patients living with multiple myeloma. Legend Biotech is seeking an Associate Director, Regulatory Affairs as part of the Regulatory Affairs team based in Somerset, NJ. Role Overview The Associate Director of...Permanent employmentFull timeTemporary workFor contractorsLocal areaWorldwideFlexible hours$217.6k - $256k
...promotional review capabilities. Position Summary: The Director, Regulatory Compliance (Promotional Review Committee) serves as a key... ...position partners closely with Commercial, Marketing, Medical Affairs, Legal, Compliance, and Market Access teams to ensure that external...Local area3 days per week$230.72k - $345k
...Full time R12948 Position Summary The Senior Director, Global Regulatory Strategy is a senior regulatory executive responsible... ...forums. Partner with Clinical Development, Medical Affairs, Regulatory CMC, Quality, Safety, Commercial, Market Access, and Program...Full timeTemporary workLocal areaRemote workWorldwideFlexible hours- ...Regulatory & Clinical Affairs Manager Princeton, NJ Permanent Qualifications: • Bachelor’s degree in engineering, Biomedical Engineering, Life Sciences, Regulatory Affairs, or related field. • 5-12 years of experience in medical device regulatory affairs...Permanent employmentFull time
- ...Job TitleJob Responsibilities:Determine international regulatory submission and approval requirementsCompile, prepare, review regulatory submission with in-country representatives and ensure on-time submission to relevant authoritiesAnticipate regulatory obstacles and...Work experience placement
$250k - $300k
...Senior or Executive Director of Biostatistics Location: Remote Therapeutic Area: Solid Tumor Oncology Salary: $250-300k Base... ...summary outputs, and contributing to clinical publications and regulatory submissions. This position will contribute to the clinical...Remote work$107k - $126k
Noom is on a mission to help people live better, longer. We're a consumer-led digital health company, connecting people to content, coaching, community, and clinicians, to build lasting habits and live healthier lives. We're a high-growth organization powered by science...Contract workFor contractorsSummer workSummer holidayWork at office2 days per week$217.52k - $263.58k
...in alignment with global GVP regulations regulatory guidance and inspectorate expectations.... ...across Patient Safety R&D Quality Regulatory Affairs IT and Legal to ensure aligned execution... ...to your Candidate Home Account. R: Director Head of PV and REMS Compliance...Hourly payFull timeSummer workLive inLocal areaRemote workWorldwideFlexible hoursNight shift$104.4k - $156.6k
...Genmab seeks a Manager of Regulatory Advertising & Promotion to oversee FDA submissions of prescription drug promotional materials, maintain... ...Bachelor's degree in life sciences, pharmacy, regulatory affairs, or related field Pharmaceutical or biotechnology industry...- ...Acadia Pharmaceuticals Inc. is seeking a Director of External Innovation to lead cross-functional diligence for clinical-stage assets... ...and value drivers. The role interfaces with Clinical, Regulatory, CMC, Commercial, Finance, Legal, and Business Development to inform...
$203.44k - $305.16k
...Then we would love to have you join us! The Role : The Director acts as a statistical expert supporting the clinical... ...may support innovation and improve efficiencies Engage with regulatory authorities on compound/indication level discussions Acts as...Full timeFixed term contract- ...Bristol Myers Squibb seeks a Director to lead pharmacovigilance and REMS compliance programs, ensuring sustained regulatory compliance and quality excellence across global patient safety operations. The role combines strategic oversight of PV processes, US REMS program...
$250k - $275k
Job Description Job Description Americans are struggling, democracy is breaking down, and there is one group of people who can, and will, rebuild our society: young leaders. The C&S team works directly with more than 1000 of the nation's most energized young changemakers...Remote workNight shift- Director, Wealth Planning & Strategy Location: Princeton, NJ or Bethesda, MD area Level: Director or Senior Director, based on experience Employment type: Full-time, in-person (Hybrid) About OneWell OneWell is an SEC-registered investment adviser serving ultra...Full timeWork at office
$196.7k - $353.4k
The Role:Moderna, Inc. is seeking a Sr. Director of Regulatory Strategy to lead Regulatory Strategy... ...technical data in partnership with RA CMC and verifies accuracy of clinical data... ...mitigations and overall plans to Regulatory Affairs the Project Team and senior management,...Permanent employmentFull timeWork at officeWork from home- Does your experience qualify you to be a Chief Revenue Officer? Are you ready to help SMBs grow via your strategic sales leadership skills? This full-time role serves multiple clients and allows you to significantly impact multiple businesses and lives. Highlights of the...Full timePart timeLocal areaRemote work
$90k - $115k
...Job Title: Regulatory Affairs Specialist - Food & Flavor Job Description This role leads regulatory oversight for a defined portfolio of food and flavor products, ensuring full compliance with U.S. and international regulations. The position serves as the regulatory...Permanent employmentWork at officeRemote work1 day per week- ...difference, every day. Executive Director, Global Program Manager... ...-stage development through regulatory submission and, in the event... ...of how clinical, regulatory, CMC, medical and commercial workstreams... ..., CMC, Nonclinical, Medical Affairs, Commercial, Finance and...Full time
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