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- ...marketing programs and associated PV regulations? If so, now is your chance to join Ascendis Pharma as our new Associate Director, Pharmacovigilance Vendor Management. Ascendis Pharma is a global biopharmaceutical company committed to making a meaningful difference in...
- ...impact on its customers, employees, and communities. The Role Help us transform and bring innovation to Drug Safety and Pharmacovigilance! Veeva is looking for an experienced Senior Consultant to join the Safety Professional Services team and support implementations...Fjernjob
- ...Sciences or Biology); a PhD and/or clinical specialist experience is considered an advantage Experience within drug safety, pharmacovigilance and/or regulatory affairs; experience with lifecycle risk management activities (e.g. RMPs, aggregate reports and labelling...
- ...Excellence, Global Patient Safety Location: Denmark / EU In this important role, you will work closely with the Director, Pharmacovigilance Process Excellence, the QPPV Office and the broader Global Patient Safety organization to ensure our pharmacovigilance system...
- ...dynamic quality team take part in the oversight and management of the compliance, quality, standards, GVP auditing and training for Pharmacovigilance. The GVP Quality team, is a part of the QA Development team with around 35 dedicated colleagues located in Hellerup, Denmark...
- ...Management, you will play a key role in improving and standardizing processes across Regulatory Affairs, Quality Assurance, and Pharmacovigilance. This is not a highly theoretical or purely strategic role. We are looking for someone with a hands-on approach to project...
- ...As a Senior Safety Manager at LINK Medical, you will play a central role in delivering high-quality pharmacovigilance services to our clients and ensuring compliance with global regulatory requirements. Key responsibilities • Focus on pre-marketing safety activities...
- ...subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document...
- ...The Business Development & Portfolio Management area covers Portfolio Strategy, Business Development, Regulatory Affairs and Pharmacovigilance. You will be reporting directly to our Chief Business Development & Portfolio Strategy Officer and partner closely with Strategy...
- ...Jobbeskrivelse Placering Søborg, Denmark Jobkategori Reg Affairs & Safety Pharmacovigilance Regulatory Affairs Professional Do you thrive in complexity, balancing strategic regulatory thinking with the pace of a rapidly evolving development programme...
- ...architecture, including technical strategy, governance and platform design ~ Demonstrated expertise architecting enterprise pharmacovigilance or safety case management platforms. Direct Vault Safety experience is a plus, not a prerequisite; the underlying architectural...
- ...Jobbeskrivelse Placering Søborg, Denmark Jobkategori Reg Affairs & Safety Pharmacovigilance Safety Surveillance Post-Marketing Cardiometabolic III Søborg, Denmark Are you driven by patient safety and scientific excellence? Do you want to influence...
- ...within Global Patient Safety (GPS). We are looking for a Quality Specialist to support the continuous improvement of the global pharmacovigilance system framework and help ensure quality oversight of the future governance setup within Global Patient Safety (GPS) in Novo...
- ...relevant degree within life sciences, nursing, pharmacy, or a related discipline and bring solid experience from drug safety/pharmacovigilance. It is a clear advantage having direct experience in Safety Operations. You may already be leading a Drug Safety Operations function...
- ...Jobbeskrivelse Placering Søborg, Denmark Jobkategori Reg Affairs & Safety Pharmacovigilance Process Excellence, QPPV Office & PV Excellence, Global Patient Safety Location: Denmark / EU In this important role, you will work closely with the Director...
- ...Jobbeskrivelse Placering Søborg, Denmark Jobkategori Reg Affairs & Safety Pharmacovigilance Regulatory Principal Specialist Shape the regulatory strategy for cardiovascular programmes that could redefine treatment for millions – and do it at a stage...
- ...with offices in Sweden, Norway, Denmark and Finland. We are now looking for a QPPV consultant to join our in-house team of Pharmacovigilance specialists in the Nordics. You will have the opportunity to work in a team of PV specialists, helping our clients with the...
- ...Jobbeskrivelse Placering Søborg, Denmark Jobkategori Reg Affairs & Safety Pharmacovigilance Regulatory Affairs Specialist Shape the regulatory future of an expanding portfolio – from early-stage molecules to global market approvals – and see your...
- ...transformation. ~ Ensure the quality and proper storage of digital data. ~ Operate in compliance with responsibilities related to pharmacovigilance and promotional regulations (CGR). Skills and Competencies: ~ Bachelor’s or Master’s degree. ~ At least 1-2 years...
- ...Jobbeskrivelse Placering Søborg, Denmark Jobkategori Reg Affairs & Safety Pharmacovigilance Senior Regulatory Affairs Professional Join us in three temporary roles where you'll shape the regulatory strategy for some of our most important pipeline...
- ...savvy approach to everyday work. Role overview In this role, you will have a broad, hands-on responsibility for Quality and Pharmacovigilance (PV) compliance activities within Théa Nordic. The position is primarily focused on Quality ownership, combined with a PV...
- ...Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the PPD Pharmacovigilance department. A day in the Life: Provide medical leadership to the study teams, including creating clinical trial...