EINFÜHRUNG Data Manager We offer an exceptional opportunity for a professional in Allschwil (Basel-Land) seeking... on clinical development, data quality, and patient safety. This organization operates globally across branded medicines, generics...
is looking a Data Manager for a initial 24 months contract based in Basel area. Main Responsibilities: Ensure Data Management... management, and protocol deviation tracking Assist in database lock activities and provide metrics to the Project Data Manager...
The Clinical Data Manager (a) will accompany and drive the phase 3 drug development by: Ensuring Data Management... pharmaceutical company in the Basel area, we are seeking a Clinical Data Manager (a) to strengthen the team in 2026 in support...
mindset If you are an experienced Data Manager looking to make a meaningful impact in clinical development, we encourage you to apply....Data Manager We offer an exceptional opportunity for a professional in Allschwil (Basel-Land) seeking a new challenge...
and manuscripts for accuracy of clinical data and content May be the Program Manager of other associates (e.g., CSE) Provides... sections of individual protocols consistent with the Integrated Development Plans (IDP), clinical data review and program...
, competitor labels, and clinical data. Ensure global consistency in labeling changes with Country Organizations. Develop..., and Dermatology, with one of the strongest Phase II/III pipelines globally. (Senior) Global Regulatory Labeling Manager The Role...
, your applications will be considered as a single submission. Johnson & Johnson Innovative Medicine R&D is recruiting for a Manager... clinical trial experience. The IH organization connects teams across development to novel capabilities and solutions...
Senior Global Labeling Manager (m/w/d) – Pharmaceutical Regulatory Affairs Shape the Future of Global Drug Labeling..., we are seeking an experienced Senior Global Labeling Manager (m/w/d). This innovative organization operates at the forefront of drug...
labels, competitor documentation, clinical study data, and regulatory frameworks - Prepare high-quality regulatory...Senior Global Labeling Manager (m/w/d) – Pharmaceutical Regulatory Affairs Shape the Future of Global Drug Labeling...
, we are rapidly advancing a clinical pipeline of anti-Claudin-1 monoclonal antibodies. Our team is committed to unlocking the broad... as kidney, liver, and lung fibrosis. Tasks The Senior CMC Regulatory Affairs Manager is responsible for defining, leading...
, we are rapidly advancing a clinical pipeline of anti-Claudin-1 monoclonal antibodies. Our team is committed to unlocking the broad... as kidney, liver, and lung fibrosis. Tasks The Senior CMC Regulatory Affairs Manager is responsible for defining, leading...
at the speed of life. The biopharmaceutical industry is undergoing a digitalization revolution, adopting data-driven R..., enabling leading biopharma, biotech, and CRDMO companies worldwide to automate processes and leverage biopharma R&D data...
. You understand the importance of Good Pharmacovigilance Practice (GVP) and Good Clinical Practice (GCP) principles and data integrity... all aspects of the end-to-end execution of clinical projects within the Roche portfolio, with the goal of developing...
. As a Client Services Project Manager I, you'll support clinical trials by managing project documentation, coordinating supply... find cures for cancer. DESCRIPTION: Join our team at Thermo Fisher Scientific and contribute to advancing clinical research...
and screening solutions in clinical practice and enable patients and healthcare providers to leverage the power of sensor data... team of scientists, technologists, data analysts and operations experts, that leverages mobile technologies...