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
$212.5k - $250k
...invite you to join us. Hybrid Employee Value Proposition Join our dynamic and expanding mid-size company in the role of Director for Regulatory CMC directly reporting to Executive Director, Regulatory CMC. Your expertise will play a pivotal and visible role in advancing...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
$224k - $271.41k
...the careers of those who do it. Role Overview The GRS-CMC Director is responsible for overseeing management of multiple development... ...Develop and communicate strategic direction based on global regulatory guidelines and experience. Seeks opportunities for external...SuggestedHourly payFull timeSummer workLive inLocal areaRemote workFlexible hoursShift work$222k - $303k
...patients, for each other, and for the future of science, we’re in. Are you?About the Role:We’re looking for a Senior Director, Regulatory Affairs CMC - Gene Therapy to help us expand what’s possible for patients with serious diseases. Reporting to the VP, Regulatory Affairs...SuggestedFull timeLocal areaRemote workFlexible hours$164.02k - $198.76k
...the careers of those who do it. Position Summary The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages... ...questions regarding drug products. The GRS-CMC Associate Director is responsible for content development, compilation,...SuggestedHourly payFull timeSummer workLive inLocal areaRemote workFlexible hoursShift work- ...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...
$266k - $346k
...every day. About the Team Kardigan’s Regulatory Affairs team is a collaborative and strategic... ...Development, Medical Affairs, Safety, CMC, Quality and other functions, the team... ...Overview Kardigan is seeking an Executive Director, Regulatory Strategy to lead global...$220k - $300k
...significant contributions to the company's success. The Regulatory Affairs (Clinical/Nonclinical) role will drive regulatory strategy and... ...regulations. The level for this role could range across Director/Sr. Director/Exec Director based on the demonstrated...$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$258.68k - $313.46k
...the careers of those who do it. Sr Director, Global Regulatory Strategy, Neuroscience Will be a... ...projects that will impact BMS, regulatory affairs or projects and provides strategies... ...or more key areas – Drug Development/CMC/Pharmtox/ Biopharmaceutics/Clinical/...Hourly payFull timeSummer workLive inLocal areaRemote workFlexible hours$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...$142.5k - $256.5k
...radically changing the biotech industry.Reporting to the Director, Regulatory Information Management (RIM), the Associate Director,... ...capabilities, and partner closely with Regulatory Affairs, Regulatory Operations, CMC, Labeling, Quality, Enterprise Data, Digital, and...Permanent employmentFull timeFor contractorsWork at officeWork from home- Regulatory and Clinical Affairs ManagerPrimary Responsibilities:Regulatory Affairs• Preparation and execution of regulatory submissions, including FDA 510(k) submissions, softwaremodifications, and international registrations as applicable.• Assess regulatory impact of...
$160k - $180k
...team success. We have an opening in our Monmouth Junction, NJ office for an experienced Associate Director or Director, Advertising & Promotions to join our Regulatory Affairs team. Title and salary commensurate with experience. This position provides senior regulatory...Full timeWork at office$137k - $167.5k
POSITION SUMMARYThe Senior Regulatory Compliance Manager is responsible for providing independent quality assurance assessment of global... ...Medicines AssetsPartner closely with Global Regulatory Affairs, Clinical Development, Clinical Operations, Pharmacovigilance,...Local areaFlexible hours$150k - $205k
...Operating at the intersection of technology, legal, and sales functions, the team specializes in translating complex and evolving regulatory landscapes into actionable guidance for externally-facing products and services. We value analytical rigor, collaborative problem...Full timeContract workSecond jobLive inWorldwideFlexible hours$217.52k - $263.58k
...alignment with global GVP regulations, regulatory guidance, and inspectorate expectations.... ...Patient Safety, R&D Quality, Regulatory Affairs, IT, and Legal to ensure aligned execution... ...Candidate Home Account. R1606559 : Director, Head of PV and REMS Compliance Data Privacy...Hourly payFull timeSummer workLive inLocal areaRemote workWorldwideFlexible hoursNight shift$242k - $315k
...internal and external audits, inspection readiness and management, regulatory surveillance, and other compliance programs and initiatives as... ...) under laws administered by the Secretary of Veterans Affairs; or a person who was discharged or released from active duty because...For contractorsRemote work$230.44k - $279.23k
...careers of those who do it. The Senior Director, Compliance Policy & Education is a... ...Resources, Enterprise Learning, Corporate Affairs, Information Technology, Quality, Internal... ...risks, business priorities, and regulatory expectations. Serve as the primary relationship...Hourly payFull timeSummer workLive inLocal areaRemote workWorldwideFlexible hours$217.6k - $256k
...Oncology’s promotional review capabilities. Position Summary The Director, Regulatory Compliance (Promotional Review Committee) serves as a key... ...partners closely with Commercial, Marketing, Medical Affairs, Legal, Compliance, and Market Access teams to ensure that external...Local area- ...Executive Director, Global Program Manager About Us Kardigan... ...late-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
$78k - $156k
...compliance with all relevant customs regulations and trade laws and regulations, including 19CFR,15CFR, FDA, USDA, and other US regulatory agency requirements.What You’ll Work OnResponsible for compliance with applicable Corporate and Divisional Policies and procedures...Shift work$97k - $189k
...matter and are part of something important, ensuring the abilities of all employees are used to their fullest potential. The Managing Director Strategic Claim Oversight leads the Severity & Excess Accounts team that both directly handles and oversees the highest exposure...Full timeWork experience placementWork at office$182.07k - $220.63k
...of patients, and the careers of those who do it. The Associate Director, Global Policy Strategy Execution will help shape and execute BMS... .... The role will operate across Global Policy and Government Affairs and the wider cross‑functional matrix, working closely with...Hourly payFull timeSummer workLive inLocal areaRemote workFlexible hours$231.28k - $346.92k
...Job Description Director, Real-World Evidence (RWE) & Epidemiology Analytics \n Location: Princeton, New Jersey \n Work Arrangement... ...analytical infrastructure while maintaining data security and regulatory compliance. \n Contribute to departmental strategy and...Full timeRemote work- Chief Philanthropy Officer About the Company Mission-driven organization providing educational services to young people Industry Education Management Type Non Profit Founded 1945 Employees 11-50 Categories ~ Education About the Role ...
$111k - $135.5k
Job SummaryManage overall batch review of sterile and OSD manufacturing/packaging records, certificates of analysis/compliance and all related supporting documentation (i.e. documentation review, SOP compliance, instrument preventive maintenance/calibration/qualification...Flexible hours- Changing lives. Building Careers.Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what...Full time
- Onsite in Plainsboro, NJ preferred (open to remote). Summary Our client has engaged GForce Life Sciences to provide a Regulatory Affairs Labeling Operations Specialist (Contractor) to support final printed pharmaceutical labeling for launch and lifecycle management initiatives...For contractorsRemote 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
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