Global Regulatory Submissions Leader, Clinical Trials
Bristol-Myers Squibb
Bristol Myers Squibb is seeking a Senior Manager, Submission Management Clinical Trials to oversee regulatory activities for clinical trial submissions. This role involves collaborating with stakeholders, preparing submissions for health authorities, and leading continuous improvement initiatives. The ideal candidate will have a minimum of 10 years of regulatory submissions experience and a BA/BS degree in a science or technology field. Join us to help drive compliance and innovation within our teams. #J-18808-Ljbffr
- ...A late clinical-stage rare disease company is seeking a Director/Senior Director of Regulatory Affairs. In this strategic role, you will manage global regulatory strategies for submissions in the US, EU, UK, and Japan. You will lead major submissions, engage with regulatory...Regulatory
$176.4k - $207.5k
Recursion is seeking an Associate Director of Regulatory Affairs to lead global regulatory strategies and oversee processes. This role requires at least 10 years of experience in the pharmaceutical industry, with 8 years in Global Regulatory Affairs. The ideal candidate...RegulatoryRemote work$122.25k - $176.58k
## Global Submission LeadBewerbenlocations: Morristown, NJ: Cambridge, MAtime type: Vollzeitposted on: Heute ausgeschriebentime left to apply... ...responsible for the planning, coordination, and tracking of regulatory Priority portfolio and Integration submission activities for...RegulatoryWorldwideFlexible hours- ...Gan & Lee Pharmaceuticals is seeking a Regulatory Affairs professional to support the implementation of regulatory strategies. Responsibilities include ensuring compliance for product submissions and regulatory interactions. The ideal candidate will have a Bachelor of...Regulatory
- ...Apr is seeking a Contract Senior Manager, Regulatory Affairs, to oversee the submission of regulatory documents to National Health Authorities. This role requires a minimum of 5 years of regulatory affairs experience in the pharmaceutical or biotechnology sector. The successful...RegulatoryContract work
$259k - $394k
...biotechnology company is seeking a Vice President of Regulatory Affairs to develop and execute regulatory strategies for global pipeline programs. The ideal candidate will... ...will be responsible for managing regulatory submissions, leading health authority interactions, and...Regulatory$160k - $241k
Tango Therapeutics is seeking a Clinical Trial Leader (CTL) to execute clinical trials in a fast-paced biotech environment. You will lead cross... ..., managing the setup and conduct of trials while ensuring regulatory compliance. This role requires strong leadership and...Regulatory- ...Praxis Precision Medicines, Inc. is searching for a Senior Regulatory Submissions Manager to oversee regulatory submissions to U.S. and international agencies. The role requires at least 7 years of experience in the pharmaceutical or biotech industry and strong management...RegulatoryRemote work
$176k - $236k
...BeiGene, Ltd. is seeking a Director, Global Regulatory Project Management, to lead oncology regulatory strategies across the drug development... ...with advanced project management; managing NDA/BLA/MAA submissions and driving cross‑functional integration globally. The ideal...Regulatory$240k - $280k
...Compensation Data Solutions Global Industry Leader - Industrial & Manufacturing This is a hybrid... .... Monitor Industry Trends and Regulatory Changes: Stay abreast of industry developments... ...be compensated in any way for your submission of a candidate, even if Aon hires...RegulatoryFull timeTemporary workPart timeLocal areaShift work$198k - $289k
...Job Description: Clinical - Standards and Digital Data Flow Leader Interested to be... ...generation of clinical trials? Then this... ...these domains at a global level. Outstanding... ...in the clinical, regulatory and safety domain.... ...ADaM, Regulatory Submission Packages and Data...Regulatory$160k - $241k
...Summary We are seeking a Clinical Trial Leader (CTL) to lead cross-functional... ...timelines, budget, regulatory requirements, and internal... ...Contribute to regulatory submissions and responses as needed. What... ...preferred). Experience working in global clinical development...RegulatoryInterim role$100k - $250k
...Quince is seeking a Global Trade Compliance Director to oversee trade compliance operations, ensuring data integrity and regulatory adherence. This role requires 12+ years of trade compliance experience and strong analytical skills. Key responsibilities include managing...Regulatory- ...GE-Vernova- seeks a Global Immigration Leader to ensure a frictionless employee experience in a complex regulatory environment. This pivotal role involves developing global immigration strategies aligned with business needs while supporting international hiring and compliance...Regulatory
- ...Framework Ventures is looking for a Head of Legal & Compliance to oversee all global legal, regulatory, and compliance matters. This role requires at least 10 years of legal experience, with a strong background in technology and blockchain, guiding the company through...Regulatory
- ...A leading global consulting firm is seeking a Senior / Principal Regulatory Compliance Consultant. This role requires expertise in QC Microbiology and aseptic drug manufacturing. The successful candidate will have 10+ years of experience in the field and will lead complex...Regulatory
- ...infection. The Safety Physician, Global Pharmacovigilance, should be... ...of adverse events from clinical trials and postmarketing surveillance... ..., Clinical Operations, Regulatory Affairs and Medical Affairs.... ...safety reports for regulator submission. Demonstrated ability to prioritise...Regulatory
- ...A global clinical research organization is seeking a highly organized Senior Regulatory Affairs Associate to coordinate regulatory submissions across regions. The successful candidate will manage submission activities, ensuring timely and compliant filings that support...Regulatory
- ...Biostatistics to join their dynamic team in Madison, NJ. This role is crucial in designing clinical trials, conducting statistical analyses, and preparing regulatory submissions that affect patients' lives. Qualified candidates should possess a PhD or MS in statistics/...Regulatory
- Nanit is looking for a Global Product Safety & Compliance Manager in New York City to oversee product safety governance and regulatory compliance across markets. The ideal candidate will have 7+ years of experience in global product safety and regulatory compliance, particularly...RegulatoryRemote jobFlexible hours
- A leading biotech firm in New York is looking for a Senior Regulatory Affairs Manager to shape its regulatory strategy across a portfolio... ...treatments. This high-impact role involves managing submissions for cosmetics, medical devices, and therapeutics, while ensuring...Regulatory
- ...Co., Ltd is seeking a physician to lead clinical development activities within their U.S.... ...involves consulting with teams to optimize trial strategies, overseeing essential clinical trials, and participating in regulatory submissions. Applicants must possess an M.D. or D.O....Regulatory
- Olympus Corporation of the Americas is seeking a Director of Global Quality Risk Management to lead the development and implementation... ...device lifecycle. This remote role ensures compliance with regulatory requirements and drives a risk culture in R&D, Quality, and other...RegulatoryRemote job
- ...investment management sector seeks a Chief Compliance Officer/ General Counsel to manage global compliance across multiple funds. This high-level role demands extensive regulatory knowledge and strong leadership skills, with a focus on improving compliance processes and...Regulatory
$176k - $236k
...Director, Global Regulatory Lead page is loaded## Director, Global Regulatory... ...regulatory requirements for clinical studies and marketing... ...Supports the preparation and submission of global regulatory documentation... ...in support of clinical trials and marketing applications,...RegulatoryHourly payTemporary workWork experience placementRemote workShift work- Kinetico Incorporated is looking for a Global Quality Director who will lead the design and implementation of the company's quality strategy... .... This role involves setting quality standards, ensuring regulatory compliance, and leading initiatives to enhance product quality...Regulatory
$122.25k - $176.58k
## Global Regulatory Affairs (GRA) Chemistry, Manufacturing and Controls (CMC) CMC LeadBewerbenlocations... ...preparing high-quality regulatory submissions, managing compliance, and anticipating... ...diverse teams spanning scientific, clinical, and digital fields, fostering...RegulatoryTemporary workWorldwideFlexible hours- Initial Therapeutics, Inc. is seeking a Director of Global Regulatory Affairs to drive ex-US regulatory strategies for clinical studies focused on oncology and rare diseases. The ideal candidate will lead IND and CTA submissions, leveraging extensive regulatory experience. A...RegulatoryRemote job
- ...biopharmaceutical company is seeking a Director of Clinical Operations to oversee the planning and execution of clinical trials. The successful candidate will manage... ...team, ensuring compliance with regulatory requirements while leading global trials. Candidates should have over 1...RegulatoryWork at officeRemote work
- CeDent is seeking a detail-oriented Regulatory Associate to join its Regulatory Affairs... ...crucial in supporting the development and submission of regulatory documents, ensuring... ...facilitating the approval process for clinical trials and product launches. This role offers...Regulatory
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