Program 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 StellenangeboteLead 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 …Expert Information 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 Information Stellenangebote
Senior 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 ScientificMedical Writer (Senior & Principal) – United States
Schwabenheim
Vollzeit
Merck Sharp & Dohme
… for Senior and Principal Medical Writers. Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and … medicine. In the role of the Senior Medical Writer: Is recognized as a scientific contributor and subject matter expert in preparation of selected … Writer: Is recognized as a scientific contributor and subject matter expert in preparation of selected regulatory clinical documentation. Applies …Pharmacovigilance Information StellenangeboteFreelance Project Manager - Technology transfer
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 … is expected. Proficient in Microsoft Word, Excel, PowerPoint. Additional information All candidates must be legally eligible to work Germany and ideally based …Expert Pharmacovigilance Scientific StellenangeboteClinical Safety Coordinator
München
Vollzeit
Medpace, Inc.
… to join our team in Munich! This position plays a key role in the pharmacovigilance process at Medpace. Working in a team to accomplish tasks and projects … global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic … success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the …Pharmacovigilance Scientific StellenangeboteGlobal Safety Scientist
Aachen
Vollzeit
Grünenthal
… or pharmacy with a doctoral degree Preferably professional experience in pharmacovigilance Good medical and scientific understanding for assessing safety data … table To make the most of this role and truly thrive, you should have: A scientific university degree in human medicine or pharmacy with a doctoral degree …Pharmacovigilance ScientificDeputy EU QPPV
Deutschland
Vollzeit
BeiGene
… EU QPPV is responsible for maintaining, overseeing and promoting BeiGene’s pharmacovigilance system and overseeing the benefit-risk profile of BeiGene’s medicinal … for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and … compliance with the EU legal requirements Ensures and verifies that the information contained in the PSMF is an accurate and up-to-date reflection of the …Expert ScientificPatient Safety Europe Lead
Deutschland
Vollzeit
BeiGene
… Representatives (LSRs) in each European country ensures that all local pharmacovigilance (PV) activities are performed as required by European and local … for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and … On- and off-boarding of European LSRs or their deputies Ensure relevant information for local PV oversight is available to the European LSRs Support …Scientific InformationQuality Manager
Homeoffice
Vollzeit
P95
… data scientists, statisticians, data analysts, medical writers, safety and pharmacovigilance specialists, project managers and business support professionals spreading … colleagues experience a strong sense of meaning and purpose driven by the scientific nature and impact of our wo …Expert Scientific StellenangeboteClinical Research Associate (CRA) Remote / Deutschlandweit (m,f,d)
München
Home Office
MSD
Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and … opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who … relevant regulations and standards Ability to serve as a subject matter expert for monitoring processes/systems and supporting the team on a local or …Information StellenangeboteSpecialist 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 … above-mentioned processes What you bring with you Successfully completed scientific studies or a comparable scientific education (e.g. Master, Pharmaceutical … which are relevant for marketing authorisation Review and evaluation of information texts for medicinal products and food supplements Interface / support of …Expert Scientific Information(Senior) Safety Data Scientist
Ingelheim am Rhein
Vollzeit
Boehringer Ingelheim
The Position Patient Safety & Pharmacovigilance is accountable for benefit/risk analysis and assessment of all BI … discipline such as computer science, bioinformatics, etc.; an advanced scientific degree (e.g., PhD, MD) is a plus Proven track record in data engineering … and patient safety purposes Has profound technical and/or domain expertise to influence and drive the data science discussions in One Medicine …Expert Pharmacovigilance Information