Administrative Assistant
Berlin
Vollzeit
ProPharma Group
… regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end … and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO … by the Manager. Provide overflow support as required for the medical information services taking detailed messages as delegated by the Manager. Quality …Scientific InformationPharmacovigilance Associate
Deutschland
Vollzeit
knoell Germany GmbH
… YOUR TASKS We are seeking a dedicated professional to oversee routine pharmacovigilance activities under the guidance of our QPPV, ensuring adherence to … development and product development support to clients. Our team of scientific and regulatory experts and extensive network of partners ensures that all … development support to clients. Our team of scientific and regulatory experts and extensive network of partners ensures that all the different …Pharmacovigilance Scientific InformationMedical 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 … will play a leading role in growing expertise, interacting with external scientific experts, and addressing business needs across regions. Key … Technical mastery in assessing scientific data and extract most relevant information Passion for innovation, discovering new trends, learning, growing …Pharmacovigilance Information
Expert* Pharmacovigilance & Scientific Information
Münster
Teilzeit
Diapharm GmbH & Co. KG
… Gewährleistung von Arzneimittelsicherheit und Evaluierung medizinischer informationen. Consulting / Beratung Funktion als EU-QPPV, Stufenplanbeauftragter und … Pharma, Medizinprodukte, Nahrungsergänzungsmittel und Kosmetik nutzen die expertise von Diapharm! Und dabei benötigen wir Ihre Hilfe! Sie übernehmen …Expert Pharmacovigilance InformationProgram Manager (remote)
Homeoffice
Vollzeit
P95
… data scientists, statisticians, data analysts, medical writers, safety and pharmacovigilance specialists, project managers and business support professionals spreading … Manager is responsible for the operational aspects of a portfolio of scientific projects (or program), ensuring the successful planning, execution, and …Expert PharmacovigilanceGlobal 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 … treatments. We focus on driving medical innovation, combining scientific and patient insights to develop and deliver safe and effective solutions. … and ensure consistency with global strategy. In addition, you provide expertise and strategic input to allow for efficient, scientifically, and …Pharmacovigilance Scientific StellenangebotePharmacovigilance Officer/ EU-QPPV* (Reporting to the Chief Medical Officer)
Deutschland
Vollzeit
AiCuris GmbH & Co. KG
Your mission At AiCuris, the role of the Pharmacovigilance Officer is of the highest importance. Bringing broad knowledge to the drug … European Commission Continuous observation of the regulatory landscape and scientific literature regarding pharmacovigilance Reviewing and amending safety … literature regarding pharmacovigilance Reviewing and amending safety information within development documents Responsible for writing and reviewing adverse …Pharmacovigilance ScientificSpecialist Pharmacovigilance (m/w/d)
Schwabenheim
Vollzeit
MSD
Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and … period of 2 years as a parental leave replacement. Your responsibilities: Scientific evaluation of global drug safety reports and electronic forwarding to the … with the line manager Collaboration on projects depending on your expertise and the need Your profile: You hold a university degree in scientific …Expert Pharmacovigilance InformationRegulatory 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 … assessment of global product development plans Initiating and conducting scientific consultations with the responsible authorities Qualifications Completed … Regulatory Affairs Expert (m/w/d) Category: Reg Affairs & Safety Pharmacovigilance Location: Mainz, …Expert Pharmacovigilance Scientific Information StellenangeboteSenior Manager Patient Advocacy (Full time OR Part time)
Hattersheim
Vollzeit
CSL Behring
… to therapy areas Ensure Medical Affairs activities (Medical Information/Pharmacovigilance/promotional material & activities) all comply with the relevant CSL … positive healthcare environment for pipeline products Develop and maintain scientific relationships with Key Opinion Leaders to build customer insight Develop … relevant to therapy areas Ensure Medical Affairs activities (Medical Information/Pharmacovigilance/promotional material & activities) all comply with the …Expert Scientific Information StellenangeboteProgram Head (Remote, full-time)
Homeoffice
Vollzeit
P95
… data scientists, statisticians, data analysts, medical writers, safety and pharmacovigilance specialists, project managers and business support professionals spreading … the projects related to the programs respective disease area, to guarantee scientific excellence of all projects within the program, contribute to the company … respective disease area(s) Provide or ensure the appropriate technical expertise in the disease area(s) within the program Oversee the preparation of …Expert Pharmacovigilance InformationLead Patient Safety Physician
Biberach an der Riß
Vollzeit
BI International GmbH
… development and post-marketing safety Comprehensive understanding of pharmacovigilance regulations in major markets and the need for compliance Broad … differentiate the asset through its benefit-risk profile, considering the scientific knowledge for the molecule, medical safety landscape, population, … applying for this location, we kindly request you to provide the necessary information at the top of your CV and proceed with the application for the position in …Pharmacovigilance Scientific StellenangeboteMedical Expert*
Mainz
Vollzeit
BioNTech AG
… are brought to the attention of the clinical development lead. Support pharmacovigilance activities (e.g. contributing to aggregate reports, patient narratives, … will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop … for a healthy future in many people's lives. Medical Expert* The Medical Expert Clinical Development is responsible for relevant aspects of clinical trial …Expert 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 … Supports Regulatory Affairs Department in the preparation of the necessary scientific information for HCPs as well as the information leaflets for patients in … is responsible for: Supporting the team in ensuring the correctness of the information material on OTC medicines for Germany, Austria and Switzerland and …Expert Pharmacovigilance Scientific Information