Pharmacovigilance Specialist
4 days ago
TN Sweden is a forward-thinking company that values diversity and inclusion in the workplace.
About the PositionWe are seeking an experienced Pharmacovigilance Specialist to join our team and contribute to our mission of making a difference in healthcare.
The successful candidate will have a strong background in Pharmacovigilance, with experience in Aggregated Reports and Signal Management. They will be responsible for maintaining oversight of Patient Safety surveillance activities, providing aggregate data and contributing to Risk Management Plans.
A key aspect of this role is ensuring high-quality and timely completion of activities under own responsibility in Safety Surveillance & Risk Management.
Key Responsibilities:
- Oversee medicinal product safety profiles and risk-benefit evaluations throughout the lifecycle.
- Ensure high-quality and timely completion of activities under own responsibility in Safety Surveillance & Risk Management.
- Maintain oversight of Patient Safety surveillance activities, providing aggregate data and contributing to Risk Management Plans.
- Perform signal validation, further signal assessment, and contribute to Company Core Safety Information (CCSI) management.
- MSc. Pharm, Medicine, or equal master in life science.
- Minimum 3 years of Pharmacovigilance experience in the pharmaceutical industry.
- Experience in Aggregated Reports and Signal Management.
- Fluent in oral and written English.
- Expert in MS office and Veeva Vault Safety.
- Knowledge of Pharmacovigilance Guidelines and Regulations.
- Able to work effectively independently and collaboratively across the organisation.
-
Deputy EU Pharmacovigilance Specialist
3 days ago
Stockholm, Stockholm, Sweden TN Sweden Full timeJob DescriptionWe are seeking a skilled Deputy EU Pharmacovigilance Specialist to join our team at TN Sweden. As a key member of our Global Patient Safety department, you will play a vital role in ensuring the safety and efficacy of our products.Key Responsibilities:Deputise for the European Union QPPV as required and according to delegation, fulfilling...
-
Pharmacovigilance Expert
4 days ago
Stockholm, Stockholm, Sweden Karo Healthcare Full timeAbout the RoleThis is an exciting opportunity to join Karo Healthcare's Pharmacovigilance team as a Global Patient Safety Surveillance Specialist.You will be responsible for maintaining an overview of medicinal product safety profiles and risk-benefit evaluations throughout the product lifecycle.Main Responsibilities:Evaluate all activities under your...
-
Medical Surveillance Professional
4 days ago
Stockholm, Stockholm, Sweden Karo Healthcare Full timeJob DescriptionWe are seeking a highly skilled Pharmacovigilance expert to join our team as a Global Patient Safety Surveillance Specialist.As a key member of our Pharmacovigilance team, you will play a crucial role in ensuring patient safety and compliance with regulatory requirements.Your Key Accountabilities:Maintain an overview of medicinal product...
-
Senior EU Regulatory Specialist
4 days ago
Stockholm, Stockholm, Sweden TN Sweden Full timeTN Sweden is a leading company in the field of pharmacovigilance, and we are seeking a talented Senior EU Regulatory Specialist to join our team. As a key member of our regulatory affairs department, you will play a critical role in ensuring compliance with regulatory requirements.Your responsibilities will include:Developing and implementing regulatory...
-
Pharmacovigilance Expert
7 days ago
Stockholm, Stockholm, Sweden Karo Group Full timeJob SummaryAs a Global Patient Safety Surveillance Specialist, you will be responsible for ensuring the high-quality and timely execution of activities within Safety Surveillance & Risk Management. You will work closely with our team to provide aggregate data, write and review reports, and contribute to risk management plans.
-
Business Growth Specialist
4 days ago
Stockholm, Stockholm, Sweden Albion Rye Associates Full timeCompany OverviewAlbion Rye Associates is a leading consultancy specializing in regulatory affairs and pharmacovigilance solutions for biotech and pharmaceutical companies. We help organizations navigate complex regulatory landscapes, ensuring compliance, and accelerating drug development and commercialization.
-
Global Pharmaceutical Risk Manager
4 days ago
Stockholm, Stockholm, Sweden Karo Healthcare Full timeAbout the RoleWe are seeking a highly skilled Medical Safety Specialist to join our team at Karo Healthcare. In this role, you will be responsible for monitoring medicinal product safety profiles and risk-benefit evaluations throughout their lifecycle.Key Skills and QualificationsMSc. Pharm, Medicine, or equal master in life science degree.Minimum 3 years of...
-
Clinical Operations Manager
3 days ago
Stockholm, Stockholm, Sweden TN Sweden Full timeCompany OverviewProPharma is a Research Consulting Organization that partners with clients across the product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting...
-
Clinical Research Specialist
2 days ago
Stockholm, Stockholm, Sweden TFS HealthScience Full timeAbout this roleWe are seeking an experienced Regulatory Compliance Officer to join our team at TFS HealthScience. As a leading global Contract Research Organization (CRO), we partner with biotechnology and pharmaceutical companies in their clinical development journey.The QPPV/Safety Manager will oversee Drug Safety management according to company policies,...
