Senior Regulatory Affairs Lead Clinical Trials
Montefiore Orthopedics
A leading healthcare institution in Bronx, New York, is seeking a Senior Regulatory Consultant to manage regulatory compliance for cancer clinical trials. This role involves overseeing the regulatory process from approval to closure and mentoring junior staff. The ideal candidate should hold a Bachelor’s degree in Life Science or Health Policy and have a minimum of 4 years of experience in Regulatory Affairs. Additional certifications such as SOCRA or ACRP are preferred, alongside strong management and communication skills. #J-18808-Ljbffr
- ...A leading cancer treatment center in New York is seeking a Senior Regulatory Compliance Coordinator to oversee clinical trials and ensure compliance with regulatory standards. You will work closely... ...years of experience in regulatory affairs or clinical research and relevant...Senior
$72k - $90k
...healthcare provider in New York is seeking a Senior Regulatory Consultant to oversee the regulatory compliance of cancer clinical trials. The role involves managing trial... ...years of experience in regulatory or clinical affairs. This position offers a salary range of $7...Senior- ...A leading cancer research institution is seeking a Senior Trial Master File Manager to oversee management and maintenance of... ...ensures quality and compliance with regulatory standards and involves team... ...over 10 years of experience in clinical operations, particularly with...SeniorContract workRemote work
- ...Health/ inVentiv Health Commercial LLC is hiring a Senior Clinical Project Manager for managing complex Phase 2b clinical trials. This remote role focuses on overseeing global... ...clinical operations, proven track record in leading international studies, and strong...SeniorRemote work
- ...Ohio State University is seeking a Senior Regulatory Compliance Officer for its Clinical Trials Office. This pivotal role ensures that investigator-initiated trials meet university, state, and federal regulations. Responsibilities include regulatory document review, provide...SeniorWork at officeRemote workFlexible hours
$64.5k - $93k
...seeking a detail-oriented editorial professional to manage content editing, proofreading, and updating materials in compliance with clinical trial protocols. You will also maintain style guides for agency and client materials. The ideal candidate will have a Bachelor’s...Senior- ...Investigo is hiring a Clinical Research Coordinator II (CRC II) in the New York City area to manage complex and high-enrolling clinical trials. The ideal candidate will have over a year of clinical research experience, strong protocol comprehension, and the ability to...SeniorHourly payFull time
$136.4k - $181.4k
...BeiGene, Ltd. is seeking a Senior Clinical Research Manager to oversee clinical monitoring activities and the performance of the CRA team. This leadership role ensures compliance with ICH-GCP, local regulations, and company standards while fostering a positive team culture...SeniorLocal area- ...BeiGene, Ltd. is seeking an AD, Regulatory Affairs CMC dedicated to developing and implementing global regulatory strategies for market access. You will manage CMC aspects through all development phases and coordinate with key stakeholders. The ideal candidate will have...Senior
- ...A pioneering life sciences company in New York is seeking a Senior Regulatory Affairs Manager to shape its regulatory strategy across a diverse portfolio including cosmetics and therapeutics. This leadership role will manage FDA and global submissions, ensuring the integration...Senior
- A biopharmaceutical company is seeking a Senior Manager, Global Regulatory Affairs Labeling to lead its global labeling initiatives. This role involves strategy development for labeling, ensuring compliance, and managing cross-functional stakeholder reviews. Candidates...SeniorRemote work
- ...A biotechnology company in New York seeks a Senior Regulatory Affairs Manager. This role involves shaping the regulatory strategy for a portfolio... .... Responsibilities include defining regulatory pathways, leading FDA filings, and ensuring integration across various teams....Senior
$115k - $185k
...A medical device company is seeking a Senior Regulatory Affairs Specialist to lead regulatory submissions and strategy for new product development. This role offers flexibility in levels and can be remote, aligned with US East Coast hours. Candidates should have a Bachelor...SeniorRemote work$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-functional teams, managing the setup... ...and conduct of trials while ensuring regulatory compliance. This role requires strong...Senior- ...EBR Systems, Inc. is hiring a Senior Clinical Research Associate in the United States to ensure study compliance and data integrity. The ideal candidate will have over five years of CRA experience on complex studies, preferably in the medical device sector, particularly...Senior
- ...Ventra-Health is seeking a Senior Regulatory Affairs Specialist in the United States. The role involves managing the Merit-Based Incentive Payment System (MIPS) for Hospital Medicine and Emergency Medicine clients, ensuring compliance, and collaborating closely with key...Senior
- ...Syneos Health/ inVentiv Health Commercial LLC is hiring a Senior Clinical Project Manager for global Phase 2b clinical trials focused on inflammation. This remote position requires expertise in global trial management, leadership, and collaboration across international...SeniorRemote workFlexible hours
- ...IQVIA in New York is seeking a Clinical Research Associate (CRA) to join our team dedicated to advancing clinical research and improving patient outcomes. In this role, you'll lead site monitoring, ensure compliance with GCP/ICH guidelines, and collaborate with cross-functional...Senior
- ...seeking a Sr. Manager, Biostatistician/Programmer to join their Clinical team. This role entails developing high-quality analyses and... ...quantitative discipline and significant experience in clinical trial analysis. This position offers a dynamic work environment with...Senior
- ...eResearch Technology Inc. is seeking a Senior Lead Clinical Project Manager for oncology studies. This role involves providing strategic leadership... ...quality. Ideal candidates will have 5-10 years of clinical trials experience, focusing on project management within CRO or...Senior
- A leading medical institution is seeking a Grant or Contract reviewer to handle grant applications, negotiate agreements, and interact with various stakeholders including faculty and funding agencies. The ideal candidate will have a Bachelor's degree and at least six years...SeniorContract work
- A leading regulatory consultancy located in New Jersey is seeking an experienced Regulatory Affairs specialist. The role involves supporting US and EU regulatory submissions while ensuring adherence to regulations concerning medical devices. The ideal candidate should have...SeniorWork at office
- A leading medical institution in New York is seeking a Grant or Contract Reviewer to evaluate grant applications and negotiate agreements. This role involves significant oversight and collaboration with various internal and external stakeholders, ensuring compliance with...SeniorContract work
- ...A leading clinical research organization is seeking a Senior Lead Clinical Data Manager to drive data strategy and lead global clinical projects. This fully remote role offers flexibility and the chance to collaborate with top-tier sponsors. Candidates should have extensive...SeniorRemote work
$110k - $135k
Integrated DNA Technologies is looking for a Regulatory Affairs Specialist to manage regulatory submissions and ensure compliance within life sciences and diagnostics. You will lead the creation of regulatory documents and provide guidance on product development while...SeniorRemote job- ...Parexel International is seeking a Senior Clinical Research Associate in Idaho to manage and monitor clinical trial sites. This role ensures compliance with regulatory standards and oversees investigator relationships to promote patient safety and study quality. A Bachelor...Senior
$85k - $167k
...A leading technology company is seeking a Program Manager / Senior Analyst to oversee the lifecycle management of sensitive U.S. government authorizations. This role requires expertise in federal assessments, guiding continuous monitoring strategies, and providing compliance...Senior- ...Conair LLC is seeking a Senior Customs & FTZ Compliance Specialist to support the Customs Manager in ensuring compliance with U.S. Customs and Trade regulations. This role will involve auditing customs entries and collaborating with external brokers to maintain accurate...Senior
$283k - $402k
...Exelixis Inc is seeking a qualified MD to lead and execute clinical trials for oncology products. The role involves working closely with clinical teams to design and monitor studies while ensuring compliance with regulations. Candidates should have extensive experience...Senior$116.72k - $175.08k
JobRx, Inc. is seeking a dedicated Pharmacist Coordinator to manage daily sterile and non-sterile compounding operations at a centralized pharmacy. This role ensures adherence to USP and FDA standards, supervising all compounding activities and ensuring high safety standards...Senior
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