Drug Safety Jobs
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Search results - Drug Safety Jobs
Appcast-London
case report forms (CRFs), statistical plans, clinical study reports/synopses, integrated summaries of safety, New Drug or Biologic License Applications (NDA/BLA), Marketing Authorization Applications (MAA), Common Technical Document (CTD) submissions...
Appcast-Great Malvern
forms (CRFs), statistical plans, clinical study reports/synopses, integrated summaries of safety, New Drug or Biologic License Applications (NDA/BLA), Marketing Authorization Applications (MAA), Common Technical Document (CTD) submissions, Regulatory...
Appcast-Cambridge
include review of specific clinical, regulatory, and scientific documents including protocols, informed consent/assent forms, case report forms (CRFs), statistical plans, clinical study reports/synopses, integrated summaries of safety, New Drug or Biologic...
Appcast-London
with adverse event (MedDRA) and drug (WHO Drug) coding for clinical and postmarketing safety data. - Demonstrate or gain knowledge of current and applicable global PV regulations and guidelines (e.g., CIOMS, EMA, FDA, ICH, etc.), SOPs and quality standards...
Appcast-City of London
documents including protocols, informed consent/assent forms, case report forms (CRFs), statistical plans, clinical study reports/synopses, integrated summaries of safety, New Drug or Biologic License Applications (NDA/BLA), Marketing Authorization...
Appcast-Great Malvern
with adverse event (MedDRA) and drug (WHO Drug) coding for clinical and postmarketing safety data. - Demonstrate or gain knowledge of current and applicable global PV regulations and guidelines (e.g., CIOMS, EMA, FDA, ICH, etc.), SOPs and quality standards...
Appcast-Cambridge
documents including protocols, informed consent/assent forms, case report forms (CRFs), statistical plans, clinical study reports/synopses, integrated summaries of safety, New Drug or Biologic License Applications (NDA/BLA), Marketing Authorization...
Appcast-London
section(s) for clinical, regulatory, and scientific documents including protocols, informed consent/assent forms, case report forms (CRFs), statistical plans, clinical study reports/synopses, integrated summaries of safety, New Drug or Biologic License...
Appcast-United Kingdom
documents including protocols, informed consent/assent forms, case report forms (CRFs), statistical plans, clinical study reports/synopses, integrated summaries of safety, New Drug or Biologic License Applications (NDA/BLA), Marketing Authorization...
Appcast-London
statistical plans, clinical study reports/synopses, integrated summaries of safety, New Drug or Biologic License Applications (NDA/BLA), Marketing Authorization Applications (MAA), Common Technical Document (CTD) submissions, Regulatory Agency responses, IRB...
Appcast-Great Malvern
/ concerns to senior management in a timely and appropriate manner.
• Mentors and trains junior members of the Medical Safety team.
Required Knowledge, Skills, and Abilities
Minimum Requirements
• At least 6 years of experience in drug safety, including...
1 similar job: London
Halstead (Essex)
Apricus Resourcing are working with a leading charitable organisation who are looking for a Lead Drug & Alcohol Nurse for a permanent post based within one of their services detox centres in Halstead.
Within your role you will join an experienced...
cv-library.co.uk -
Roche-Welwyn
of individual and aggregate case reporting, encompassing ICSR case management and critical aggregate reporting activities like DSUR and PBRER.
• Drive signal detection and management, and contributing to the strategic review of safety assessments and drug...
roche.com -
City of London
the process for safety signal management activities (detection, evaluation, prioritisation, and assessment of safety signals related to drug safety), writing aggregate reports (PSURs, DSURs, Line Listings, RMPs), responding to safety questions from internal...
cv-library.co.uk -
City of London
Scientist is responsible for overseeing and leading the process for safety signal management activities (detection, evaluation, prioritisation, and assessment of safety signals related to drug safety), aggregate reports (PSURs, DSURs, Line Listings, RMPs...
cv-library.co.uk -
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