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Pharmacovigilance Jobs

1 - 15 of 72
1 - 15 of 72
Search Results - Pharmacovigilance Jobs
Elanco-Auckland
A global leader in animal health is looking for a Pharmacovigilance Associate in Auckland, New Zealand. In this role, you'll ensure compliance with pharmacovigilance regulations, manage safety reporting, and collaborate across teams for product...
Cloudbyz Inc-Greymouth
Project Manager – Life Sciences (Pharmacovigilance) Location: West Coast, USA Job Type: Full-time About the Role We are seeking a highly motivated Project Manager with deep experience in pharmacovigilance and life sciences to lead cross-functional...
Elanco Tiergesundheit AG-Auckland
A leading animal health company is seeking an APAC Pharmacovigilance Leader in Auckland. Key responsibilities include overseeing PV activities, leading the team, and ensuring compliance with APAC regulations. Candidates should have at least 5 years...
Cloudbyz Inc-Westport
Project Manager – Life Sciences (Pharmacovigilance) Location: West Coast, USA Job Type: Full-time About the Role We are seeking a highly motivated Project Manager with deep experience in pharmacovigilance and life sciences to lead cross-functional...
Elanco-Auckland
to new heights. Making animals’ lives better makes life better – join our team today! Your Role: As the Pharmacovigilance Associate, you will be part of the regional PV team supporting New Zealand and acting as Deputy for Australia. In this role, you...
Cloudbyz Inc-Hokitika
Project Manager – Life Sciences (Pharmacovigilance) Location: West Coast, USA Job Type: Full-time About the Role We are seeking a highly motivated Project Manager with deep experience in pharmacovigilance and life sciences to lead cross-functional...
University of Otago-Auckland
A leading New Zealand university is seeking a Medical Assessor to join its national Centre for Adverse Reactions Monitoring (CARM) in Dunedin. The role involves reviewing reports on adverse reactions to therapeutic products and applying clinical...
Syneos Health-Stratford
subject confidentiality; assesses factors affecting subject safety and data integrity at investigator sites, including protocol deviations/violations and pharmacovigilance issues.Per CMP/SMP: assesses site processes, conducts Source Document Review...
University of Otago-Auckland
NEW ZEALAND PHARMACOVIGILANCE CENTRE Applications are invited for a Medical Assessor to join the national Centre for Adverse Reactions Monitoring (CARM). About us/Mō mātou CARM is contracted by Medsafe (the New Zealand Medicines and Medical Devices...
Syneos Health-Fairlie
subject confidentiality; assesses factors affecting subject safety and data integrity at investigator sites, including protocol deviations/violations and pharmacovigilance issues.Per CMP/SMP: assesses site processes, conducts Source Document Review...
Syneos Health-Te Kuiti
subject confidentiality; assesses factors affecting subject safety and data integrity at investigator sites, including protocol deviations/violations and pharmacovigilance issues.Per CMP/SMP: assesses site processes, conducts Source Document Review...
Syneos Health-Napier
subject confidentiality; assesses factors affecting subject safety and data integrity at investigator sites, including protocol deviations/violations and pharmacovigilance issues.Per CMP/SMP: assesses site processes, conducts Source Document Review...
Syneos Health-Hawera
subject confidentiality; assesses factors affecting subject safety and data integrity at investigator sites, including protocol deviations/violations and pharmacovigilance issues.Per CMP/SMP: assesses site processes, conducts Source Document Review...
Syneos Health-Rotorua
subject confidentiality; assesses factors affecting subject safety and data integrity at investigator sites, including protocol deviations/violations and pharmacovigilance issues.Per CMP/SMP: assesses site processes, conducts Source Document Review...
Syneos Health-Dunedin
subject confidentiality; assesses factors affecting subject safety and data integrity at investigator sites, including protocol deviations/violations and pharmacovigilance issues.Per CMP/SMP: assesses site processes, conducts Source Document Review...
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