194 regulatory associate jobs at 94 companies in Wyncote, PA
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Regulatory Reporting - Associate
Newark, Delaware, United States
OnsiteFull Time
3+ YOE3+ years relevant experience in regulatory/wholesale loans or credit risk reporting; strong Excel and PowerPoint; Tableau and Alteryx experience; understanding of regulatory reporting and financial statements.
Tableau, Alteryx, Microsoft Excel, Microsoft PowerPoint
1mo
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Senior Associate, Regulatory Operations
Philadelphia, Pennsylvania, United States
$26-$34/hr OnsiteTemporary
2+ YOEBachelor's degree and 2+ years preparing complex regulatory/promotional submission deliverables; strong Adobe Acrobat and Microsoft Office skills; excellent communication, organization, and technical writing.
Adobe Acrobat, Microsoft Office Suite, Adobe InDesign, Adobe Photoshop
6d
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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
3mo
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Senior Associate, Regulatory Affairs
Philadelphia or San Francisco
OnsiteFull Time
2+ YOEBachelor’s in life sciences; 2+ years Regulatory Affairs in biotech/pharma; oncology/IND experience; strong communication; regulatory submissions; FDA/ICH knowledge.
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
2d
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(Associate) Director, Regulatory Operations
Philadelphia, Pennsylvania, United States
HybridFull Time
8+ YOERequires 8+ years in Regulatory Operations, global submission planning, eCTD and ICH expertise, regulatory or document management systems experience, vendor management, and ability to build processes independently.
Veeva RIM Basics, ZenQMS, eCTD, ICH, FDA, EMA, MHRA, Health Canada
2mo
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Associate Director Regulatory Affairs, Oncology
Upper Providence or Waltham or Rockville or Durham or Cambridge or San Francisco
$139k-$231k/yr HybridFull Time
Develop and execute regional regulatory strategies for oncology assets, lead regional submissions and interactions with regulatory authorities, ensure compliance across product lifecycle, and work cross-functionally within global matrix teams.
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.
1w
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Regulatory Coordinator I
Allentown, Pennsylvania, United States
OnsiteFull Time
1+ YOEAssociate degree required, or high school diploma with 1–2 years of regulatory or administrative experience. Requires Microsoft Office, organizational skills, attention to detail, and multitasking ability.
Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft Access, Microsoft Outlook, Internet Functions, Excel, IND, NCTN, NIH COI tutorial, CITI GCP, CAP, CLIA
1mo
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Senior Associate, Regulatory Operations
Philadelphia, Pennsylvania, United States
$26-$34/hr HybridTemporary
2+ YOEBachelor's degree and 2+ years preparing complex submission deliverables; strong Adobe Acrobat and Microsoft Office skills, attention to detail, organization, and clear technical writing.
Adobe Acrobat, Microsoft Office Suite, Adobe InDesign, Adobe Photoshop
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
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
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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.
2mo
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Associate Director, Regulatory Affairs, CMC
United States or Philadelphia or Cambridge
$171k-$231k/yr HybridFull Time
8+ YOEAdvanced degree in a relevant scientific discipline, 8+ years industry experience including 5+ years in Regulatory Affairs CMC, experience with regulatory submissions and health authority interactions, strong communication and cross-functional leadership.
1mo
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Associate Director, Promotional Regulatory Affairs
Gaithersburg or Wilmington
$150k-$225k/yr HybridFull Time
5+ YOE5+ years regulatory affairs experience in pharma/biotech, working knowledge of FDA promotional regulations, Bachelors in pharmacy/life sciences preferred, experience with electronic review tools and VEEVA PromoMats.
VEEVA PromoMats
2mo
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Associate Director, Regulatory Affairs - Biosimilars (US)
Princeton, New Jersey, United States
$146k-$279k/yr HybridFull Time
7+ YOEBachelor's degree in life sciences and 7+ years of biopharmaceutical regulatory affairs experience, including US biosimilar programs, 351(k) BLA submissions, FDA interactions, and cross-functional leadership.
IND, BLA, FDA, Biosimilar Product Development (BPD), 351(k)
2mo
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Associate Director, Regulatory Affairs - Biosimilars (US)
Princeton, New Jersey, United States
$146k-$279k/yr HybridFull Time
7+ YOE7+ years regulatory affairs in biopharma with US biosimilar experience; FDA submissions; strong cross-functional leadership and communication.
1mo
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Associate Manager, Regulatory Advertising & Promotion
Sleepy Hollow or Warren
$110k-$179k/yr HybridFull Time
1+ YOE1–2 years regulatory affairs experience (advertising & promotion preferred),BS required; advanced scientific degree preferred; knowledge of advertising/promotion regulations; experience interacting with FDA OPDP; strong written/verbal skills.
4d
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Research Regulatory Coordinator, Full Time,
Moorestown or Voorhees or Marlton
$26-$39/hr HybridFull Time
3+ YOERequires 3+ years supporting clinical research regulatory activities, IRB applications, investigator documentation, and protocol approvals; strong organization and communication skills; associate degree required, bachelor's preferred.
Institutional Review Board (IRB), FDA 1572, Virtua
3mo
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Associate Director, Regulatory Affairs Project Planning & Coordination
Princeton or San Diego or San Francisco
$154k-$193k/yr HybridFull Time
8+ YOEBachelor’s degree in life science; 8+ years regulatory drug development; global submissions experience; willing to travel.
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