Pharmacovigilance Manager
3 weeks ago
R&D Partners is seeking a Pharmacovigilance Manager to join a pharmaceutical organization based in London. In this role, you will focus on ensuring the safety of medicines and compliance with regulatory requirements. This is an excellent opportunity for someone passionate about drug safety and patient well-being. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: Oversee and manage drug safety processes to ensure compliance with regulations. Monitor and evaluate the safety of medicines, identifying and addressing any risks. Prepare and review safety reports and documentation. Collaborate with internal teams and external partners to maintain high safety standards. Ensure timely reporting of safety information to regulatory authorities. Key Skills and Requirements: Strong understanding of pharmacovigilance principles and regulations. Ability to analyze and interpret safety data effectively. Excellent communication and organizational skills. Experience in managing safety processes and working with cross-functional teams. Proficiency in relevant software and tools used in pharmacovigilance. For more information, please contact William Tyler . If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -
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Pharmacovigilance Manager
2 weeks ago
Slough, United Kingdom R&D Partners Full timeR&D Partners is seeking a Pharmacovigilance Manager to join a pharmaceutical organization based in London. In this role, you will focus on ensuring the safety of medicines and compliance with regulatory requirements. This is an excellent opportunity for someone passionate about drug safety and patient well-being. Please note that to be considered for this...
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Pharmacovigilance Manager
1 week ago
Slough, Slough, United Kingdom Hobson Prior Full time £65,000 - £85,000 per yearHobson Prior is seeking a Pharmacovigilance Manager to join a pharmaceutical organization based in London. In this role, you will focus on ensuring the safety of medicines and compliance with regulatory requirements. This is an excellent opportunity for someone passionate about drug safety and patient well-being.Please note that to be considered for this...
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Senior Drug Safety
2 weeks ago
Slough, United Kingdom R&D Partners Full timeA leading life sciences recruiter is seeking a Pharmacovigilance Manager to oversee drug safety processes and ensure compliance with regulations. The ideal candidate will have a strong understanding of pharmacovigilance principles, excellent communication skills, and experience managing safety processes. This position offers an exciting opportunity to...
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Head of Pv Innovation
2 weeks ago
Slough, United Kingdom UCB Full time**Make your mark for patients** We are looking for a **Head of Pharmacovigilance Innovation** to join us in our **Global Pharmacovigilance** team, based in any of our Brussels (Belgium), Slough (UK) or Raleigh (US) offices. **About the role** Reporting to the Head Vigilance, Systems & Innovation, as member of their leadership team (LT), the Head...
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GCP Quality Specialist
2 weeks ago
Slough, United Kingdom Planet Pharma Full timeWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a strong focus on...
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GCP Quality Specialist
4 weeks ago
Slough, United Kingdom Planet Pharma Full timeWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a strong focus on...
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GCP Quality Specialist
1 week ago
Slough, United Kingdom Planet Pharma Full timeWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a strong focus on...
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GCP Quality Specialist
2 weeks ago
Slough, United Kingdom Planet Pharma Full timeJob DescriptionWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a...
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Senior Process Quality Excellence Specialist
2 weeks ago
Slough, United Kingdom Next-Link Full timeOverview The Senior Process Quality Excellence Specialist (SPQES) will support the Head of Process Quality Excellence (HPQE) for GCSO in developing and maintaining its clinical quality systems / procedures and ensuring quality and compliance risks are appropriately identified and mitigated. Activities include all aspects of clinical studies that are managed...
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GCP Quality Specialist
1 week ago
Slough, Slough, United Kingdom Planet Pharma Full time £60,000 - £90,000 per yearWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a strong focus on...