14 pharmacovigilance associate jobs at 10 companies in California
1w
Save
Mark Applied
Hide
Pharmacovigilance / Drug Safety Associate
South San Francisco, California, United States
$125k-$150k/yr OnsiteFull Time
2+ YOEBachelor's degree in life science, nursing, pharmacy, or related discipline; 2–5 years in pharmacovigilance, drug safety, clinical research, or related biotechnology, pharmaceutical, or CRO work; clinical-trial safety experience preferred.
Microsoft Office, XpressCF®, Clinical database, Global safety database
2mo
Save
Mark Applied
Hide
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
2mo
Save
Mark Applied
Hide
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
1w
Save
Mark Applied
Hide
Associate Director, Medical Safety
South Boston or Boston or San Francisco or Zug or London
$170k-$190k/yr HybridFull Time
6+ YOEMD, DO, PharmD, or equivalent clinical degree; 6+ years of pharmacovigilance, drug safety, or clinical safety experience; ICSR medical review, causality assessment, signal detection, and global PV regulations knowledge.
CRISPR/Cas9, PRR, ROR, EBGM, DSUR, PBRER, PSUR, GVP Module IX, FDA, ICH E2, Argus, ArisGlobal, Veeva Vault Safety, CAR-T, ASTCT, FDA, EMA, PMDA/MHLW, NMPA/CDE
1w
Save
Mark Applied
Hide
Associate Director, Safety Data Sciences
Illinois or California or South San Francisco or Irvine or Florham Park
$142k-$269k/yr HybridFull Time
2+ YOERequires a health sciences degree, 4 years of experience with a bachelor's or 2 years with a master's/doctorate, pharmacovigilance knowledge, drug development expertise, communication, and project management skills.
Microsoft Word, Microsoft Excel
1w
Save
Mark Applied
Hide
Associate Director, Safety Data Sciences
Lake County or Irvine or South San Francisco or Florham Park or North Chicago
$142k-$269k/yr HybridFull Time
2+ YOEHealth sciences degree plus 2–4 years of clinical, pharmaceutical, or safety experience; pharmacovigilance expertise, drug development knowledge, communication skills, and Microsoft Word and Excel proficiency.
Microsoft Word, Microsoft Excel
2mo
Save
Mark Applied
Hide
Associate Director, GVP Compliance
Dublin or Shanbally or London or Novato
HybridFull Time
8+ YOE8+ years in regulated healthcare quality/compliance with pharmacovigilance (GVP) experience; knowledge of FDA/EMA/ICH/GCP; experience with inspections, audits, QMS; strong communication, strategic thinking, and MS Office skills; Bachelor's in life sciences (master's preferred).
Microsoft Office
1w
Save
Mark Applied
Hide
Associate Director, Safety Data Sciences
Illinois or Irvine or South San Francisco or Florham Park or Illinois or California or New Jersey
$142k-$269k/yr HybridFull Time
2+ YOEHealth sciences degree plus 2–4 years of clinical, pharmaceutical, or safety experience; pharmacovigilance knowledge; drug development expertise; communication, project management, Microsoft Word, and Microsoft Excel skills.
Microsoft Word, Microsoft Excel
1w
Save
Mark Applied
Hide
Associate Director, Safety Data Sciences
Illinois or Irvine or South San Francisco or Florham Park or North Chicago
$142k-$269k/yr HybridFull Time
2+ YOEHealth sciences degree; bachelor's plus 4 years or master's/doctorate plus 2 years of clinical, pharmaceutical, or safety experience. Requires pharmacovigilance knowledge, safety analysis, communication, and Microsoft Word and Excel skills.
Microsoft Word, Microsoft Excel
2mo
Save
Mark Applied
Hide
Associate Medical Director
San Diego or United States
$210k-$250k/yr HybridFull Time
5+ YOEMD with 5+ years in drug safety/pharmacovigilance, experience reviewing ICSRs (causality/expectedness), familiarity with Argus or similar safety databases, knowledge of FDA/EMA/ICH guidance, strong clinical judgment and communication.
Argus
2mo
Save
Mark Applied
Hide
Associate Clinical Safety Surveillance Director
Research Triangle Park or Durham or California or United States
HybridFull Time
7+ YOE3+ MgmtExtensive pharmacovigilance experience in end-to-end ICSR case processing, clinical trial safety oversight, vendor management, SOP development, MedDRA coding, Argus experience preferred, and people management.
Argus, MedDRA
2w
Save
Mark Applied
Hide
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
Save
Mark Applied
Hide
Associate Director, Program Safety Lead - Job ID: 1908b
Palo Alto, California, United States
$200k-$215k/yr HybridFull Time
6+ YOEPharmD required,6+ years pharmacovigilance experience,leadership in safety,endocrinology experience,clinical medicine exposure preferred,professional English,ability to travel up to 20%.
3w
Save
Mark Applied
Hide
Associate Director, Medical Safety Science (Safety Scientist)
Foster City, California, United States
$215k-$230k/yr HybridFull Time
7+ YOEBachelor's degree in a scientific discipline and 7+ years in pharmaceutical or CRO settings, including 5+ years in drug safety and pharmacovigilance. Requires safety surveillance, aggregate reporting, and adverse-event coding review experience.
Safety Database, clinical database