Regulatory Launch Accelerator & Enablement Lead
Sanofi
Sanofi seeks a Launch Acceleration and Regulatory Enablement Lead to build a new function that accelerates regulatory submissions across Global Business Units, driving awareness, tools, and capabilities. You will be a thought leader and hands‑on trainer, influencing senior governance forums and cross‑functional teams between Morristown, NJ and Cambridge, MA. You will shape submission strategies, reuse content, and innovate with AI and digital tools to modernize regulatory workflows. #J-18808-Ljbffr Sanofi
- ...Job title : Launch Acceleration and Regulatory Enablement Lead ~ Location: Morristown, NJ/Cambridge, MA About the job Innovation doesn't happen by doing more of what we've always done. This role is for a regulatory professional who is ready to challenge assumptions...RegulatoryShift work
- ...HCP action and prescribing behavior. You will lead a data-driven, integrated strategy to accelerate diagnosis, treatment initiation and brand uptake in a competitive launch. Strong cross-functional leadership and regulatory collaboration are essential. #J-18808-Ljbffr...Regulatory
- Novartis is seeking a Program Manager to coordinate platform strategy and launch enablement for priority commercial product launches in a hybrid role based in East Hanover, NJ. You will align technology, data, CRM, analytics, and platform teams to ensure timely delivery...Suggested
- ...Transplantation Medical Publications Lead Location: Morristown, NJ... ...of Sanofi data, enabling safe, appropriate use of and... ...external scientific, legal and regulatory standards. Performs other duties... ...of drug development and post-launch/marketed products Experience...RegulatoryWork at office
$178.5k - $257.83k
...Real World Evidence Scientific Lead** *Location: Morristown, NJ,... ...- and innovative pipeline - enables us to invent medicines and vaccines... ...for the registration, pre-launch and peri-launch of teplizumab... ...intended use, whether for regulatory, market access or clinical use...Regulatory$127k - $168k
...technology, tools, and teams that enables innovators to build and scale... ...with confidence. Trusted by leading AI labs, startups, and global... ...deep technical expertise to accelerate breakthroughs and turn... ...equity.Monitor market trends and regulatory changes (e.g., pay transparency...RegulatoryPermanent employmentFull timeTemporary workCasual workWork at officeFlexible hours- Teva, a leading biopharmaceutical company with a strong biosimilars franchise, seeks a Director... ...portfolio from development through launch and lifecycle management. You will act as a key link across Commercial, R&D, Regulatory, Finance, Supply Chain, Manufacturing/Technical...Regulatory
- Job title: Biostatistics Franchise Lead Location: Morristown, NJ / Morristown, NJ / Waltham... ...immune system and innovative pipeline enables us to invent medicines and vaccines that... ...by design practice, functional review of regulatory documents and ensure translation of biostatistical...RegulatoryFor contractors
$185.5k - $344.5k
...Transformations team is dedicated to enabling improved decision making at... ...Discovery & Innovation: Lead discovery initiatives, design... ...industry, including regulatory requirements, market dynamics... ...Skills Inspirational Leadership Launch Products Marketing Strategy Media...RegulatoryWorldwide- ...title : Senior Director, Americas Region Lead, Diversity & Inclusion in Clinical Trials... ...immune system - and innovative pipeline - enables us to invent medicines and vaccines that... ...indicators (KPI) contact. Stay current on regulatory requirements in the region, industry best...RegulatoryLocal area
- ...Novartis? Please read on... Program Manager, Platform Strategy & Launch Enablement Novartis is seeking a Program Manager, Platform Strategy &... ...Program Management & Delivery Coordination Lead program management activities across technology and data initiatives...Contract workTemporary workFor contractorsRemote work
$204.4k - $379.6k
...Director, Medical Value & Enablement (MVE) is a highly... ...Director is expected to lead through expertise, influence... ...correction mechanisms to accelerate progress while managing... ...Pharmaceutics Product Launches Real World Evidence (RWE) Regulatory Compliance Research Methodologies...RegulatoryLocal areaImmediate start- LEO Pharma is seeking an Associate Director, Specialty Pharmacy & Trade Relations to lead specialty pharmacy, patient affordability, and trade strategies for a rare disease brand in launch preparation. You will build the capabilities, processes, and partnerships needed to...
- Shionogi Inc. in Florham Park, NJ seeks an Associate Director to lead analytics driving customer insights and strategic discussions.... ...help shape the quarterly business review process for the XOCOVA launch. You will provide analytics to forecast demand, analyze market dynamics...
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- Shionogi Inc. is seeking a Senior Manager/Associate Director of Regulatory Affairs CMC to define and execute global CMC regulatory... ...content with a risk-based approach. Responsibilities include leading global CMC strategies, coordinating timelines, liaising with Health...Regulatory
$146k - $209k
Execution Lead, ERP DeliveryLocation: Parsippany, NJ (Hybrid)About Zoetis:Zoetis is the... ...ensuring alignment with business objectives, regulatory requirements, and enterprise governance... ..., Cutover, and Hypercare ManagementAI-Enabled Delivery Tools and PracticesBusiness Process...RegulatoryFull timeTemporary workLocal area- ...Affairs team to advance strategic medical initiatives and ensure launch readiness for the myeloma portfolio. You will work cross-... ...functionally with Field Medical, Commercial, Market Access, HEOR/RWE, Regulatory, and Global Medical Affairs to translate data into actionable...Regulatory
- DescriptionThe Lead Analyst will work under the supervision of a consultant or project manager to assist with developing solutions... ...assessments that evaluate impacts associated with rules implemented by regulatory agencies.Assists with designing, reviewing, and modifying...RegulatoryContract workWork at office
- ...clinical operations content to clinical and regulatory documents (e.g., INDs, IB, NDAs, BLAs,... ...programs can be 20-200 million dollars) Leads large scoped, cross-functional innovation... ...operations (direct and indirect) staff to enable growth into leadership roles, including...RegulatoryWork experience placementLocal areaRemote work
$178.5k - $257.83k
...Strategy & AI Innovation to lead precision marketing... ...strategies that accelerate franchise growth. Join... ...innovative pipeline – enables us to invent medicines... ...Commercial, Medical Affairs, Regulatory, and IT teams to align... ...product launches and lifecycle management...Regulatory- ...displayed at the store to support accurate pricing of products. Ensures any additional pricing tasks related to local regulations and/or regulatory compliance programs are completed accurately and within the required time frame. Assist with bookkeeping activities, including...RegulatoryWork experience placementSeasonal workLocal areaShift work
- ...company, seeks a Senior Legal Counsel, Global Privacy, to lead the worldwide privacy program and advise on privacy, data... ...in Parsippany, NJ partners with stakeholders to ensure regulatory compliance while enabling growth. 5+ years' privacy-focused legal experience and JD...RegulatoryWorldwide
$18 - $20 per hour
...Pay Range: $18 - $20/hour POSITION SUMMARY: The Shift Lead is responsible for executing restaurant operations, in conjunction... ...while ensuring compliance with policies, procedures, and regulatory requirements. KEY DUTIES/RESPONSIBILITIES: Maintains brand...RegulatoryLocal areaShift workWeekend work- ...Myers Squibb in New Jersey seeks a Director, Medical Evidence Generation Lead for Cardiovascular to shape strategy across clinical trials, RWE, and ISRs, coordinating with Medical Affairs, Regulatory, and cross-functional partners. You will lead study design, governance,...Regulatory
- ...execution, and tracking per SRC approval. The role reports to the Senior Manager, ESR Operations and requires collaboration across product supply, regulatory, and clinical teams to drive efficient delivery of research agreements and study milestones. #J-18808-Ljbffr BioSpaceRegulatory
- ...compliant reviews and milestone tracking. You will partner with SRC and cross-functional teams to manage study start-up, contracting, regulatory documentation, and reporting while upholding SOPs and governance across the ESR program; this role requires clear communication,...Regulatory
- Teva Pharmaceuticals is a leading biopharmaceutical company with a strong biosimilars portfolio. The Director, Portfolio Management,... ...time while ensuring supply. This role links Commercial, R&D, Regulatory, Finance, Supply Chain, Manufacturing, and Marketing in a cross...Regulatory
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