14,808 drug safety jobs at 3,323 companies in United States
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Drug Safety Physician
Princeton, New Jersey, United States
$150k-$250k/yr OnsiteFull Time
5+ YOE5+ years in Drug Safety/Pharmacovigilance; MD; oncology/hematology experience preferred; strong US/EU regulatory knowledge; experience with DSUR/PBRER/PSUR and risk management.
2mo
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Senior Specialist, Drug Safety
South Boston, Massachusetts, United States
$105k-$115k/yr OnsiteFull Time
5+ YOEBachelor’s degree in nursing, pharmacy, or other life sciences; 5+ years ICSR processing experience; knowledge of FDA/ICH/EU regulations; MedDRA/WHO Drug dictionaries; Veeva/EDC experience.
MedDRA, WHO Drug dictionaries, Veeva safety database, EDC systems
1mo
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Vice President Drug Safety
United States
$405k-$430k/yr RemoteFull Time
15+ YOE10+ MgmtMD required; 15+ years pharmacovigilance experience with ≥10 years in senior leadership; expertise in safety surveillance, signal detection, regulatory reporting (FDA/EMA/ICH/GCP).
ARGUS, MedDRA
6d
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Sr Drug Safety Scientist
Lake Zurich or Illinois
$133k-$146k/yr HybridFull Time
8+ YOERequires a current medical or clinical professional credential, 8+ years of drug safety and adverse event reporting experience, regulatory expertise, critical thinking, leadership, and Aris Global, MedDRA/WHO, and Microsoft Office knowledge.
Aris Global, MedDRA, WHO Drug, Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, LifeSphere MultiVigilance, KabiSafe LSMV, Global Complaint Management Workflow (gCMW)
4d
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Associate Director, Drug Safety Physician
South San Francisco, California, United States
$225k-$270k/yr OnsiteFull Time
8+ YOE3+ MgmtMD or equivalent advanced degree; 8–12 years of drug safety and pharmacovigilance experience; 3–4 years leading safety teams; oncology, precision medicine, regulatory, signal detection, and cross-functional expertise.
MedDRA, WHO-DD, ICH, FDA, EMA, GVP, ADCs
1mo
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Drug Safety Associate
San Diego, California, United States
$77k-$90k/yr OnsiteFull Time
1+ YOEBA in a life science or related field; 1+ years relevant clinical research or pharmacovigilance experience; clinical credential preferred (RN, PharmD, PA); knowledge of SAE/SUSAR, MedDRA, ICH GCP; proficiency with Microsoft Office.
MedDRA, Trial Master File (TMF), Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Microsoft Outlook
1mo
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Manager, Global Drug Safety & Pharmacovigilance
Cary, North Carolina, United States
$120k-$130k/yr HybridFull Time
5+ YOEBachelor's in life sciences/nursing/pharmacy,5+ years pharmaceutical drug safety/pharmacovigilance,Argus experience preferred,vendor/CRO management,knowledge of ICSR processing and global PV regulations,MS Office proficiency.
Argus, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Adobe Pro
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Director, Drug Safety & Pharmacovigilance
San Diego or Pasadena
$206k-$255k/yr HybridFull Time
8+ YOE5+ MgmtAdvanced nursing degree or PharmD required, 8+ years drug safety experience, 5+ years managing case review/signal detection, 4+ years clinical experience; experience with signaling, aggregate report authoring, Argus and MedDRA, strong knowledge of global PV and regulatory requirements.
Argus, MedDRA
1mo
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Drug Safety Associate I
Norwood, Massachusetts, United States
RemoteFull Time
3+ YOEBachelors in pharmacy/nursing/life sciences,3+ years PV/clinical research experience,MedDRA knowledge,ICH E2B/E2A and FDA/EMA reporting familiarity,attention to detail and strong written English for narrative authoring.
Veeva Vault Safety, Oracle Argus, ARISg, MedDRA, WHODrug Global, Microsoft Excel, Microsoft Word, E2B(R3)
1mo
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Executive Director, Drug Safety & Pharmacovigilance
Boulder, Colorado, United States
$275k-$350k/yr HybridFull Time
15+ YOE10+ MgmtMD/DO or equivalent,15+ years pharmaceutical experience with ≥10 years in drug safety/pharmacovigilance; deep knowledge of GCP,GVP,ICH; strong leadership, data evaluation and benefit-risk expertise.
2mo
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Director, Drug Safety & Pharmacovigilance
San Diego, California, United States
$206k-$255k/yr HybridFull Time
8+ YOE5+ MgmtOversee safety monitoring and PV processes for assigned products; lead aggregation, signaling, and regulatory submissions; collaborate cross-functionally; minimum advanced nursing degree or PharmD with extensive PV leadership experience.
Argus Safety
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Director/Senior Director, Pharmacovigilance and Drug Safety (Safety Scientist)
Needham or Boston
$223k-$318k/yr HybridFull Time
9+ YOE8+ MgmtHealth care professional degree (e.g., RN/BSN/MSN, NP, PharmD); 9+ years pharma drug safety/pharmacovigilance experience (Director) or 12+ (Senior Director); management experience; MedDRA and Argus experience; regulatory knowledge (FDA/EMA/ICH).
Argus Safety Database, MedDRA
2mo
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Director, Drug Safety and Pharmacovigilance
Brisbane, California, United States
$292k-$315k/yr OnsiteFull Time
5+ YOEMD/DO or Doctorate with 5+ years in Drug Safety and Pharmacovigilance; strong regulatory knowledge; leadership; analytical/problem-solving skills.
MedDRA, ARGUS
2w
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Director/Senior Director, Drug Safety & Pharmacovigilance
Austin or San Francisco
$235k-$310k/yr RemoteFull Time
4+ YOE4+ years pharmacovigilance/drug safety experience in pharma/biotech, oncology experience, medical safety assessment, signal detection, CRO/vendor oversight, global PV regulations, Phase 2/3 support, strong communication and independent operation.
2w
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Director, Global Drug Safety & Pharmacovigilance Physician
Princeton, New Jersey, United States
$236k-$354k/yr HybridFull Time
12+ YOEMD with 12+ years in drug safety/pharmacovigilance (clinical development and post-marketing), experience with global PV regulations, BLA/NDA submissions, regulatory inspections, and mentoring.
ARISg, ARGUS, MedDRA, WHODrug, electronic data capture systems
1mo
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Senior Manager, Drug Safety and Medical Monitor
Rockville, Maryland, United States
$131k-$155k/yr OnsiteFull Time
3+ YOEDegree in a medical field (MD/DO/MBBS/NP or equivalent) with ≥3 years relevant experience; medical monitoring and safety review experience; knowledge of MedDRA/WHO Drug, ICH/FDA regulations; experience with Veeva and clinical/safety databases; SOP authoring.
Veeva Systems, MedDRA, WHO Drug
2w
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Associate Director, Non-clinical Drug Safety
United States
$169k-$253k/yr RemoteFull Time
7+ YOEMSc/PhD in toxicology/pharmacology,7+ years pharma/CRO experience in nonclinical safety,regulatory document preparation,GLP toxicology study oversight; DABT and biologics experience preferred.
6d
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Sr Hazardous Drug Program Spec
Rochester, New York, United States
$64k-$96k/yr OnsiteFull Time
3+ YOEBachelor's degree in a related field and 3 years of hazardous materials, drug handling, industrial hygiene, or safety experience; equivalent education and experience accepted.
USP <800>, Centers for Medicare and Medicaid Services' Conditions of Participation, Joint Commission, Occupational Safety and Health Administration
1mo
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Forensic Drug Chemist
Pearl, Mississippi, United States
OnsiteFull Time
3+ YOEBachelor's in chemistry or equivalent, 3+ years bench experience in an ISO/IEC 17025 forensic drug lab, formal casework training, knowledge of GC, GC/MS, FTIR, lab safety, and ability to travel within Mississippi.
Color Tests, Gas Chromatography (GC), Gas Chromatography-Mass Spectrometry (GC/MS), Fourier-Transform Infrared Spectroscopy (FTIR), microscope
5d
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Safety Engineer
St. Louis, Missouri, United States
FieldFull Time
2+ YOEBachelor's degree in occupational health and safety, industrial engineering, or related field, plus 2 years supporting safety responsibilities. Requires pre-employment assessment and drug screening.
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