Associate Director, Pharmacovigilance Specialist
3 weeks ago
We are seeking an experienced Associate Director, Pharmacovigilance Scientist to join our team at Pharmiweb. This role will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases.
Key Responsibilities:- Conduct signal detection activities in line with approved safety surveillance plans.
- Evaluate signals and author safety evaluation reports.
- Manage preparation and review of safety documents, including DSUR, PSUR, RMP, and responses to health authority queries.
- Prepare and deliver presentations at Signal Management Team meetings and participate in clinical study team meetings.
- Participate in risk management activities and represent the team on cross-functional committees.
- Actively participate in process improvement initiatives, such as developing and maintaining relevant SOPs, WIs, and supporting documents.
To be considered for this opportunity, you must have:
- A Master's, PhD, or PharmD degree.
- 10+ years of relevant safety-related experience in the pharmaceutical/biotech industry or health authority.
We offer a competitive salary range of $170,000 to $277,500 per annum.
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Senior Pharmacovigilance Director
4 weeks ago
Uxbridge, United Kingdom Pharmiweb Full timeJob Title: Associate Director, Pharmacovigilance ScientistAt Pharmiweb, we are seeking a highly skilled Associate Director, Pharmacovigilance Scientist to join our Global Patient Safety team. As a key member of our team, you will play a critical role in developing and implementing safety strategies for molecules in clinical development and post-marketing...
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Senior Pharmacovigilance Director
4 weeks ago
Uxbridge, United Kingdom Pharmiweb Full timeJob Title: Associate Director, Pharmacovigilance ScientistAt Pharmiweb, we are seeking a highly skilled Associate Director, Pharmacovigilance Scientist to join our Global Patient Safety team. As a key member of our team, you will play a critical role in developing and implementing safety strategies for molecules in clinical development and post-marketing...
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Associate Director, Pharmacovigilance Specialist
4 weeks ago
Uxbridge, United Kingdom Pharmiweb Full timeJob Summary:We are seeking an experienced Associate Director, Pharmacovigilance Scientist to join our team at Pharmiweb. This role will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases.Key Responsibilities:Conduct signal detection activities in line with approved safety surveillance...
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Associate Director, Pharmacovigilance Specialist
4 weeks ago
Uxbridge, United Kingdom Pharmiweb Full timeJob Summary:We are seeking an experienced Associate Director, Pharmacovigilance Scientist to join our team at Pharmiweb. This role will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases.Key Responsibilities:Conduct signal detection activities in line with approved safety surveillance...
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Senior Pharmacovigilance Director
3 weeks ago
Uxbridge, United Kingdom Regeneron Full timeJob Title: Associate Director, Pharmacovigilance ScientistThe Associate Director, Pharmacovigilance Scientist will play a key role in developing and implementing safety strategies for molecules in clinical development and post-marketing phases. This will involve reviewing, analyzing, and interpreting safety data to generate appropriate safety messaging and...
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Senior Pharmacovigilance Director
3 weeks ago
Uxbridge, United Kingdom Regeneron Full timeJob Title: Associate Director, Pharmacovigilance ScientistThe Associate Director, Pharmacovigilance Scientist will play a key role in developing and implementing safety strategies for molecules in clinical development and post-marketing phases. This will involve reviewing, analyzing, and interpreting safety data to generate appropriate safety messaging and...
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Senior Pharmacovigilance Director
3 weeks ago
Uxbridge, United Kingdom Regeneron Full timeJob Title: Associate Director, Pharmacovigilance ScientistThe Associate Director, Pharmacovigilance Scientist will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases, under the guidance of the safety lead. This will include review, analysis and interpretation of safety data (including aggregate...
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Senior Pharmacovigilance Director
3 weeks ago
Uxbridge, United Kingdom Regeneron Full timeJob Title: Associate Director, Pharmacovigilance ScientistThe Associate Director, Pharmacovigilance Scientist will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases, under the guidance of the safety lead. This will include review, analysis and interpretation of safety data (including aggregate...
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Uxbridge, United Kingdom Pharmiweb Full timeJob SummaryPharmiweb is seeking a highly skilled and experienced Associate Director in Global Patient Safety to join our team. This pivotal role within our Global Patient Safety organization will focus on Case Evaluation & Reporting, ensuring efficient vendor and case processing to meet regulatory standards.As an Associate Director in GPS, you will play a...
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Director of Global Pharmacovigilance Operations
3 weeks ago
Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full timeRegeneron Pharmaceuticals Inc. Job OpportunityWe are seeking an experienced professional to join our Global Patient Safety organization as an Associate Director in the Case Evaluation & Reporting area.Key Responsibilities:Coordinate pharmacovigilance operations to ensure efficient vendor and case processing, meeting regulatory standards.Play a key role in...
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Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full timeRegeneron Pharmaceuticals Inc. Job OpportunityWe are seeking an experienced professional to join our Global Patient Safety organization as an Associate Director in the Case Evaluation & Reporting area.Key Responsibilities:Coordinate pharmacovigilance operations to ensure efficient vendor and case processing, meeting regulatory standards.Play a key role in...
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Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full timeRegeneron Pharmaceuticals Inc. Job OpportunityWe are seeking an experienced professional to join our Global Patient Safety organization as an Associate Director in the Case Evaluation & Reporting area.Key Responsibilities:Coordinate pharmacovigilance operations to ensure efficient vendor and case processing, meeting regulatory standards.Play a key role in...
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3 weeks ago
Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full timeRegeneron Pharmaceuticals Inc. Job OpportunityWe are seeking an experienced professional to join our Global Patient Safety organization as an Associate Director in the Case Evaluation & Reporting area.Key Responsibilities:Coordinate pharmacovigilance operations to ensure efficient vendor and case processing, meeting regulatory standards.Play a key role in...
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Director of Global Pharmacovigilance Operations
3 weeks ago
Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full timeRegeneron Pharmaceuticals Inc. Job OpportunityWe are seeking an experienced professional to join our Global Patient Safety organization as an Associate Director in the Case Evaluation & Reporting area.Key Responsibilities:Coordinate pharmacovigilance operations to ensure efficient vendor and case processing, meeting regulatory standards.Play a key role in...
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2 weeks ago
Uxbridge, United Kingdom Regeneron Full timeThe Senior Pharmacovigilance Director will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases, under the guidance of the safety lead. This will include review, analysis and interpretation of safety data (including aggregate data) to generate appropriate safety messaging and benefit-risk...
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Uxbridge, United Kingdom Regeneron Pharmaceuticals, Inc Full timeRegeneron Pharmaceuticals, Inc. Seeks Associate Director in Global Patient SafetyRegeneron Pharmaceuticals, Inc. is seeking an experienced Associate Director to join our Global Patient Safety organization. This pivotal role will coordinate pharmacovigilance operations, ensuring efficient vendor and case processing to meet regulatory standards.Key...