Hell's Kitchen • 50 milesRemote · Hybrid · Onsite · Field · All Environments
Hell's Kitchen • 50 milesRemote · Hybrid · Onsite · Field · All Environments
Hell's Kitchen • 50 milesRemote · Hybrid · Onsite · Field · All Environments
Hell's Kitchen • 50 milesRemote · Hybrid · Onsite · Field · All Environments
375 regulatory associate jobs at 191 companies in Hell's Kitchen, NY
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Regulatory Reporting Associate
Stamford or Orlando or Providence or Toronto or United States or Canada or North America
$90k/yr HybridFull Time
3+ YOE3+ years in regulatory/compliance/risk functions, working knowledge of regulatory frameworks, strong analytical and stakeholder skills, ability to interpret regulations, and proficiency with Microsoft Office (Excel, Word, PowerPoint).
Microsoft Office, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
2d
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Regulatory & Compliance - Associate
New York City or Greenwich
$70k-$95k/yr HybridFull Time
2+ YOERequires 2–5 years of registered investment adviser experience, preferably regulatory filings, alternative investment and private placement compliance knowledge, stakeholder leadership, project management, and Microsoft Office proficiency.
Microsoft Excel, Microsoft Word
1mo
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Regulatory Affairs Associate
New York City, New York, United States
$60k-$70k/yr RemoteFull Time
2+ YOECoordinate policy development and maintenance, maintain documentation and review cycles, support compliance initiatives, audits, training, and policy implementation; associate degree required, 2–4 years preferred.
Microsoft Office Suite
3mo
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Sr Associate Regulatory Affairs
Berkeley Heights, New Jersey, United States
$90k-$125k/yr OnsiteFull Time
5+ YOEManage ANDA and post-approval submissions (eCTD), support lifecycle and combination-product regulatory strategy; 5+ years pharmaceutical regulatory affairs experience; bachelor\u0002s in pharmacy/chemistry/biology required; eCTD, MS Word, Excel, Adobe Acrobat experience; cGMP knowledge.
eCTD, Microsoft Word, Microsoft Excel, Adobe Acrobat
4d
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Associate, Regulatory Affairs- Labeling
Princeton or Hawthorne or New Jersey
$95k-$105k/yr OnsiteFull Time
1+ YOEBachelor's degree in a scientific field, 1–3 years of generic pharmaceutical regulatory experience, advanced computer skills, strong writing and communication skills, and ability to work independently.
Artwork Management System (AMS), FDA, SPL, ANDA
1w
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Associate Manager, Regulatory Affairs
Florham Park, New Jersey, United States
OnsiteFull Time
6+ YOEBachelor's degree preferred in life science, six years of relevant experience, English proficiency, FDA regulatory knowledge, original ANDA experience preferred, and proficiency with office, regulatory, database, and eCTD tools.
Microsoft Office Suite, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Microsoft Teams, Microsoft SharePoint, Adobe Acrobat, Electronic Common Technical Documents (eCTD), eCTD Compilation software, database systems
2mo
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Regulatory Affairs Senior Associate
Rockaway, New Jersey, United States
OnsiteFull Time
6+ YOE6-10+ years of medical device regulatory experience; strong knowledge of FDA, EU MDR, UK MDR, MDSAP, Health Canada, TGA; regulatory submissions and technical documentation expertise; cross-functional leadership.
Microsoft Office, Adobe/PDF tools, regulatory databases, eQMS
3mo
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Associate Director, Regulatory CMC
Palo Alto or Princeton or Miami
$194k-$199k/yr HybridFull Time
6+ YOEBachelor’s degree in chemistry, pharmacy, engineering, or biochemistry; 6+ years Regulatory CMC experience; experience with biologics; strong FDA/EU regulatory knowledge; experience preparing CMC submissions (IND/IMPD/BLA/MAA). Mandarin desirable.
Microsoft Word, Microsoft Excel, Document management systems
1mo
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Regulatory Associate Investment Management
New York, New York, United States
$92k-$157k/yr OnsiteFull Time
7+ YOEBachelor's degree, 7+ years project management and financial services experience, knowledge of OCC/SEC fiduciary requirements, strong project, analytical, and communication skills, proficiency in Microsoft Excel and PowerPoint.
Microsoft Excel, Microsoft PowerPoint
1mo
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Regulatory Affairs Associate
Staten Island, New York, United States
$20-$28/hr OnsitePart Time
Knowledge of GCP/ICH/HIPAA, working knowledge of medical terminology and clinical research processes; HS diploma required, two-year degree preferred; clinical research experience preferred; strong Microsoft Office skills and attention to detail.
Microsoft Office
1w
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Associate Director, Regulatory Compliance
New York City, New York, United States
$130k-$150k/yr HybridFull Time
4+ YOEBachelor’s degree, 4–6 years of compliance experience, Series 24 license, Series 7 preferred or obtainable within 12 months, regulatory knowledge, strong communication, organization, and documentation skills.
Microsoft Office, MCO, Global Relay, Co-Pilot
1mo
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Associate Director, Regulatory Operations
Parsippany, New Jersey, United States
$141k-$194k/yr HybridFull Time
8+ YOEBachelor's in life sciences, 8+ years in regulatory operations (pharma/biotech), Veeva RIM SME, global submission planning/tracking, MS Word/Excel/PowerPoint, project management tools, training and process improvement experience.
Veeva RIM, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project, Smartsheet
2mo
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Associate Director Global Regulatory Sciences - Oncology
Princeton or Cambridge
$173k-$210k/yr OnsiteFull Time
4+ YOEPharmaceutical regulatory experience; advanced scientific degree preferred; 4+ years pharma experience with 3+ years in regulatory affairs; experience preparing IND/NDA/BLA submissions and leading regulatory interactions with health authorities.
1mo
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Associate Director, Regulatory Operations
Parsippany, New Jersey, United States
$141k-$194k/yr OnsiteFull Time
8+ YOEBachelor's in life sciences,8+ years regulatory operations in pharma/biotech,expertise in submission planning/tracking and Veeva RIM,project management and training experience.
Veeva RIM, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project, Smartsheet
2mo
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Associate Director, Regulatory Affairs - CMC
Warren, New Jersey, United States
$169k-$213k/yr HybridFull Time
7+ YOEBachelor's in science, 7+ years regulatory affairs/CMC writing experience in pharma/biotech, small-molecule CMC expertise, GMP knowledge, ICH/regulatory guidance familiarity, Microsoft Office proficiency, up to 10% travel.
Microsoft Office, eCTD
1mo
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Regulatory Reporting Operations- Associate
New York, New York, United States
$65k-$103k/yr OnsiteFull Time
4+ YOEExperience with regulatory transaction reporting (CAT/CFTC), strong control and risk focus, 4+ years relevant experience, knowledge of trade lifecycle, project/change management, excellent communication.
Alteryx, Power Apps, UiPath
2mo
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Insurance Transactional + Regulatory Associate - New York or Chicago
New York City or Chicago
$295k-$350k/yr OnsiteFull Time
4+ YOEJD required; 4–6 years insurance regulatory experience analyzing regulatory issues, counseling on licensing, product evaluation, form filing and financial examinations; strong research, writing, and analytical skills.
3w
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Regulatory Coordinator Assistant
Teaneck, New Jersey, United States
$27-$37/hr OnsiteFull Time
1+ YOEHigh school diploma required (associate preferred). Minimum 1 year clinical trials/regulatory/oncology experience. Knowledge of GCP, ICH, FDA, EMA. Strong attention to detail, multitasking, and communication skills.
eRegulatory systems, Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), OncoEMR, Microsoft Word, PowerPoint, Microsoft Excel, PDF, Microsoft Teams, Zoom, Google Meet, internet applications
2mo
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Associate Director, Regulatory Strategy
South San Francisco or Princeton
$170k-$230k/yr HybridFull Time
6+ YOEBachelor's in life sciences required; 6+ years regulatory affairs experience in biotech/pharma; experience with INDs/CTAs and eCTD submissions; knowledge of FDA/EMA/ICH guidance; strong communication and organizational skills.
eCTD
1mo
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Associate Director, Commercial Regulatory Affairs
Princeton, New Jersey, United States
$173k-$210k/yr OnsiteFull Time
3+ YOEBS required (advanced degree preferred); 3-5 years regulatory promotional review or 5-8 years pharma experience; experience with promotional risk assessment and OPDP interactions; strong communication and analytical skills.
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