Specialist Regulatory Affairs & Pharmacovigilance Stellenangebote

Regulatory Affairs Specialist Frankfurt am Main Vollzeit PrimeVigilance … We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global … services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our … Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support …Regulatory Affairs Specialist Medical Writing & Advice (m/f/x) Böblingen Vollzeit Wörwag Pharma … and food supplements Interface / support of Regulatory Affairs and Global Pharmacovigilance in medical/scientific issues Editing/review of technical information and … medicinal products and food supplements Interface / support of Regulatory Affairs and Global Pharmacovigilance in medical/scientific issues Editing/review … which are relevant for marketing authorisations in accordance with regulatory and internal specifications for European and global marketing …Affairs Pharmacovigilance StellenangeboteSenior Associate Medical Affairs CE Kreis Neuss Vollzeit Kenvue … concerns on the OTC drugs. Supporting the departments for pharmacovigilance and regulatory affairs in the preparation of relevant medical/clinical … Description Kenvue is currently recruiting for: Senior Associate Medical Affairs CE This position reports into the Senior Associate Manager Medical Affairs … on the OTC drugs. Supporting the departments for pharmacovigilance and regulatory affairs in the preparation of relevant medical/clinical texts. …Regulatory Pharmacovigilance

Senior Specialist Global Pharmacovigilance (m/w/d) Schwabenheim Vollzeit MSD … animal health challenges. We are looking for a Senior Specialist, Global Pharmacovigilance to join our team in Schwabenheim. This position offers a permanent, … regulated pharmaceutical field, ideally pharmacovigilance or regulatory affairs of advantage Strong analytical, communication and writing skills … in a highly regulated pharmaceutical field, ideally pharmacovigilance or regulatory affairs of advantage Strong analytical, communication and writing skills …Regulatory Affairs StellenangeboteSpecialist Regulatory Affairs & Pharmacovigilance (all genders) Hamburg Ausbildung Chiesi Farmaceutici Abteilung: Pharmaceutical Affairs Team: R&D, Pharmacovigilance & Regulatory Affairs Stellentyp: Direkter Mitarbeiter Vertragsart: … Abteilung: Pharmaceutical Affairs Team: R&D, Pharmacovigilance & Regulatory Affairs Stellentyp: Direkter … Abteilung: Pharmaceutical Affairs Team: R&D, Pharmacovigilance & Regulatory Affairs Stellentyp: Direkter Mitarbeiter Vertragsart: Vorübergehend …Regulatory PharmacovigilanceEU-QPPV & Head QPPV Office (d/f/m) Holzkirchen Vollzeit Sandoz … countries with local QPPV requirements together with GDD and Regional Pharmacovigilance/Quality Head. To contribute (as a member) to the Medical Safety Review … To ensure timely and quality preparation (together with PV, Regulatory Affairs (RA) and Medical Safety) the appropriate medical input to PV reports … as required. To ensure timely and quality preparation (together with PV, Regulatory Affairs (RA) and Medical Safety) the appropriate medical input to PV …Specialist Regulatory Pharmacovigilance StellenangeboteEngagement Manager - R&D (Remote) Berlin Vollzeit Veeva Systems … or more critical areas such as Clinical Development, Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. What You’ll Do Lead multiple project … on one or more critical areas such as Clinical Development, Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. What You’ll Do … you will focus on one or more critical areas such as Clinical Development, Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. What …Specialist Regulatory Pharmacovigilance StellenangeboteMedical Affairs Manager (m/f/d) Schwalbach am Taunus Vollzeit Procter & Gamble … professionals (HCPs), consumers & other external parties. Supporting Pharmacovigilance activities. Ensuring compliance with recognized medical and ethical … experience in Pharma/ Healthcare Industry preferable in area of medical affairs Excellent German and English language skills Strong strategic thinking and … innovations. Internally support product Life Cycle Management including regulatory, claims innovation and scientific support Drive the scientific …Specialist Affairs Stellenangebote(Junior) Pharmacovigilance Officer (w/f/d) Global Drug Safety Frankfurt am Main Vollzeit Merz Therapeutics Temporary Position for 18 months YOUR CONTRIBUTION Join our Pharmacovigilance Group within Global Product Safety and grow with new challenges. Your … the UK (e.g., AMG, AMWHV, GVP) Basic knowledge in the field of Regulatory Affairs for medicinal products is appreciated Willingness to engage in ongoing … "Stufenplanbeauftragte". Tracking and analysis of updates in legal and regulatory PV requirements and the development of implementation initiatives and PV …Specialist Affairs Pharmacovigilance StellenangeboteGlobal Medical Advisor Rheumatology / Gastroenterology Straße Vollzeit BI International GmbH … teams, e.g., Marketing, Market Access, Patient Advocacy Groups, Pharmacovigilance, and Regulatory Affairs, providing medical input. Furthermore, you … You are medically responsible for the disease and asset-related Medical Affairs strategy, its implementation in Global Plans and guidance on executional … Marketing, Market Access, Patient Advocacy Groups, Pharmacovigilance, and Regulatory Affairs, providing medical input. Furthermore, you contribute to the …Regulatory Affairs Pharmacovigilance Stellenangebote Regulatory Affairs Expert (m/w/d) Mainz Vollzeit Novo Nordisk, Inc. Regulatory Affairs Expert (m/w/d) Category: Reg Affairs & Safety Pharmacovigilance Location: Mainz, Rheinland-Pfalz, DE Life is change - improving lives is … Regulatory Affairs Expert (m/w/d) Category: Reg Affairs & Safety Pharmacovigilance Location: … our path. Do you have experience in driving strategies and initiatives in Regulatory Affairs and can you demonstrate proven success in influencing health and …Specialist Regulatory StellenangeboteAssociate Clinical Operations Manager (Regulatory) (m/f/d) München Vollzeit MSD Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and … partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas … language Informed Consents and translations. Interact with IRB/IEC and Regulatory Authority for assigned protocols. Manages country deliverables, timelines …Regulatory Affairs StellenangeboteHead QPPV & PRRC Office (f/m/d) Wehr Vollzeit Novartis … has the dual accountability of (1) acting as the EU Qualified Person for Pharmacovigilance (QPPV) and UK QPPV including the responsibility for the global Novartis … Management experience regarding managing a Patient Safety or Regulatory Affairs team (line or functional management) Excellent stakeholder management … combined medical devices and (2) heading the QPPV & Person Responsible for Regulatory Compliance (PRRC) Office. The role reports to the Head Patient Safety & …Specialist RegulatoryPharmaceutical Scientist - Pharmacovigilance Operations (m/f/d) München Vollzeit Daiichi Sankyo Europe GmbH … on ICSR case handling. Performing Data Management of Clinical Safety & Pharmacovigilance (CSPV) information of ICSR from clinical trials and marketed products. … to coordinate case processing tasks. Cooperate and support Regulatory Affairs Department with regard to safety aspects during submission and maintenance … associated quality and training activities are performed to ensure regulatory timelines and global standards are met. This includes AE report intake, …Specialist Regulatory Affairs Pharmacovigilance