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Pharmacovigilance Associate - Remote Position
Los Angeles, California, United States
$70k-$85k/yr RemoteFull Time
1+ YOE1–2 years pharmacovigilance experience, proficiency in safety databases, MedDRA/WHO Drug coding, knowledge of global PV regulations (ICH/FDA/EMA), and a bachelor’s degree in life sciences or equivalent experience.
safety databases, MedDRA, WHO Drug, E2B(R3)
1mo
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Associate Director, Pharmacovigilance Scientist
United States
$204k-$213k/yr RemoteFull Time
7+ YOEAdvanced degree required; PharmD or PhD preferred; 7+ years pharmacovigilance experience; strong regulatory knowledge; leadership in signal detection; experience with DSUR/PSUR/PBRER; excellent communication; willing to travel.
MedDRA, DSUR, PSUR, PBRER, ISS, EBGM, PRR
6d
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Associate Medical Director, Pharmacovigilance
Bothell, Washington, United States
$222k-$294k/yr OnsiteFull Time
3+ YOE2+ MgmtMD/DO or equivalent, 3+ years combined clinical and pharmacovigilance experience (2+ years leadership), global PV knowledge, safety signal detection, regulatory submission experience.
1mo
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Associate Director, Pharmacovigilance
Boston, Massachusetts, United States
$160k-$240k/yr HybridFull Time
8+ YOEBachelor's degree in a relevant healthcare field, 8+ years PV operations experience, expert knowledge of global PV requirements/ICH/GVP, MedDRA and Argus experience, vendor oversight, aggregate reporting, audit experience, strong communication and cross-functional skills.
MedDRA, Argus
1mo
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Sr. Manager/Associate Director, US Pharmacovigilance
New York City, New York, United States
$175k-$215k/yr HybridFull Time
6+ YOEBachelor's in a medical field required (Master preferred), 6+ years pharmacovigilance experience, FDA regulatory knowledge, ICSR/SAE review, safety report writing, vendor management, and cross‑functional collaboration.
1mo
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Associate Director, Safety and Pharmacovigilance
Emeryville, California, United States
$170k-$200k/yr HybridFull Time
8+ YOEBachelor's in a scientific/medical field required; 8+ years pharmacovigilance experience with PV operations and clinical safety; expertise in Argus, MedDRA, signal detection, aggregate reports, and global PV regulations.
Argus, MedDRA
2w
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Associate Director, Pharmacovigilance/ Product Safety
Bridgewater, New Jersey, United States
$179k-$233k/yr RemoteFull Time
3+ YOE3-5 years pharmacovigilance or safety officer experience in pharma; Masters in life sciences or RN/PharmD/MD; expert regulatory knowledge, MedDRA experience, strong leadership and communication skills.
MedDRA
6d
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Specialist, Pharmacovigilance
Pittsburgh, Pennsylvania, United States
$19-$26/hr OnsiteFull Time
2+ YOE2+ years healthcare/pharmacy experience preferred; associate degree or equivalent experience; proficiency with Microsoft Word, PowerPoint, SharePoint, Excel; strong communication and quality/QA skills.
Microsoft Word, Microsoft PowerPoint, Microsoft SharePoint, Microsoft Excel
2mo
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Associate Director/Director, Drug Safety & Pharmacovigilance (Quality & Compliance)
San Diego, California, United States
$180k-$230k/yr OnsiteFull Time
10+ YOE10+ years in pharmacovigilance with 9–10 years QA/compliance; BS in a related science; global PV regulatory knowledge; leadership and mentoring; audit/inspection experience; strong communication; PV software proficiency.
Pharmacovigilance databases, PV software
4w
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Associate Director, Pharmacovigilance Scientist
Waltham, Massachusetts, United States
$162k-$223k/yr HybridFull Time
Deciphera Pharmaceuticals: Developing targeted kinase inhibitors for the treatment of cancer.
5+ YOE5+ years PV experience (incl. 3+ years as PV Scientist), advanced degree required (PharmD/MD/PhD/MPH/MS/etc.), experience with signal management and aggregate reports, regulatory submission experience (NDA/MAA), strong communication and attention to detail.
Microsoft Office Suite, Argus Safety
2mo
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Associate Director, Drug Safety and Pharmacovigilance
United States
$165k-$197k/yr RemoteFull Time
10+ YOE10+ years in drug safety/pharmacovigilance; life science degree; global safety regulations; Argus/ARIS-G; DSUR/PSUR/PBRER; MedDRA/WHODrug; strong communication and leadership.
Argus, ARIS-G, electronic data capture systems, Trial Master File, MedDRA, WHODrug, MS Office
2mo
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Associate Returnship Program
United States
HybridFull Time
6+ YOEPharmacovigilance professional with 6-9 years experience, strong R&D safety ops, Excel proficiency; PV case processing experience a plus; hybrid/rotational shifts.
MS Excel
2mo
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Associate Director - Pharmacovigilance (PV) Systems Strategy and Implementation
Indianapolis, Indiana, United States
$116k-$169k/yr OnsiteFull Time
2+ YOEBachelor's preferred in health science or IT; 2+ years supporting drug development, data/reporting, and systems implementations; experience in PV or clinical research; authorized to work in the U.S.
e2B, eDC, AI, Machine Learning, Natural Language Processing, Computer System Quality (CSQ)
1mo
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Associate Director, R&D Quality Good Pharmacovigilance Practice
United States
$143k-$193k/yr RemoteFull Time
8+ YOEBachelor of Science and 8+ years pharmacovigilance experience required; expert knowledge of GVP/GCP; audit/inspection readiness, QA systems, vendor oversight, KPI development, and global regulatory compliance.
Microsoft 365, Veeva, SumTotal, ACE Audit utopia, Smartsheet
1w
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Safety Associate
Durham, North Carolina, United States
$45k-$112k/yr HybridFull Time
1+ YOEProcess safety data per SOPs/regulations, perform pharmacovigilance tasks, complete trainings, use safety databases, and communicate with teams;1-1.5 years relevant experience and medical terminology knowledge.
ARGUS, Microsoft Office
3w
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Patient Safety Associate Medical Director
Boston, Massachusetts, United States
$200k-$300k/yr HybridFull Time
3+ YOEMD/DO or equivalent medical degree required; typically 3 years safety/pharmacovigilance experience; expertise in pharmacovigilance, ICSR and aggregate safety analysis; regulatory interactions and medical safety leadership.
1mo
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Associate Director, GVP Compliance
Shanbally or Dublin or London or Novato or Ireland
HybridFull Time
8+ YOE8+ years in regulated healthcare quality/compliance with pharmacovigilance (GVP) experience; auditing and inspection experience; bachelor’s in life sciences required; strong strategic, communication and MS Suite skills.
MS Suite, Quality Management Systems
1w
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Drug Safety Associate
Pennington, New Jersey, United States
$110k-$120k/yr OnsiteFull Time
2+ YOEBachelor's in life sciences/pharmacy/nursing or related, 2+ years pharmacovigilance/drug safety experience, MedDRA coding, case triage, narrative writing, data entry and quality review.
MedDRA
4w
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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
2mo
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Associate Director, Global Safety Lead
Cambridge or United States
$185k-$309k/yr HybridFull Time
3+ YOEMD/DO with 3+ years in safety or clinical development; pharmacovigilance expertise; global regulatory knowledge; strong communication; cross-functional collaboration.
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