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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 Projects & Collaborations . Ascendis Pharma is a global biopharmaceutical company committed to making a meaningful...
- ...opportunities to standardize, simplify, and scale processes, tools, and ways of working while supporting applicable GxP, regulatory, pharmacovigilance, documentation, training, inspection-readiness, and records-management requirements. You will also provide project-...
- ...governance activities, including Data Safety Monitoring Boards, Safety Monitoring Committees, medical information escalations, pharmacovigilance oversight, and 24-hour medical support as required. Serve as Global Safety Physician, project lead, or medical safety...
- ...The Business Development & Portfolio Management area covers Portfolio Strategy, Business Development, Regulatory Affairs and Pharmacovigilance. You will partner closely with Strategy, the Strategy & PPMO Office, People & Culture and other corporate functions. Why should...
- ...Jobbeskrivelse Placering Søborg, Denmark Jobkategori Reg Affairs & Safety Pharmacovigilance Job Title: Director, Safety Operations Department: Safety Operations, Global Patient Safety, Research & Development Location: Søborg, Denmark Your...
- ...Jobbeskrivelse Placering Søborg, Denmark Jobkategori Reg Affairs & Safety Pharmacovigilance . Your impact begins here Join us as a Senior Regulatory Affairs Professional and help turn scientific innovation into medicines that can reach patients...
- ...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...
- ...testing, or compliance documentation · Exposure to GxP, computer system validation, GAMP 5, EU Annex 11, FDA 21 CFR Part 11, pharmacovigilance, medical affairs, clinical systems, or commercial life science systems is considered a strong advantage, but not an absolute...
- ...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...
- ...International Markets Commercialization, Global Medical Affairs, Clinical Development, Regulatory Affairs, Market Access, Commercial, Pharmacovigilance, Medical Operations, Compliance, Legal, Technical Operations, and other enabling functions. Ensure cross-functional...
- ...optimal data presentation. Collaborate across Medical & Science, Regulatory Affairs, Clinical Operations, Biostatistics, and Pharmacovigilance to ensure accurate, complete, and scientifically sound reporting. We are globally oriented and you will work in close...
- ...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...