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Suchergebnisse: 51 Stellenangebote
- ...role the client would like the candidate to be on side 80%. Coordinate and manage complex calendars across time zones, including scheduling... ...retrieval and confidentiality Assist in strategic project coordination, including scheduling, documentation, and tracking...EmpfohlenTemporär
- ...focus. In Vivo Sciences is responsible for the Animal Care and Use Program in pRED and thus a key business enabler for all in vivo studies. The Opportunity Are you passionate about animal welfare and scientific research? Do you enjoy working in a dynamic team...EmpfohlenTemporärInvalidenversicherung
- ...of preclinical development, continuing through clinical First in Human and Phase 1b/2 studies. As a Clinical Program Leader, you have the critical responsibility to lead and coordinate planning, execution, and interpretation of oncology early phase clinical trials....Empfohlen
- ...trials – and continuing to product maturity. Our organization coordinates all aspects of production of Roche medicines in all disease areas... ...the development of synthetic molecules from first-in-human studies through commercialization. Based in Basel, Switzerland, our team...EmpfohlenPostdoc StelleLehrstelle
- ...trials – and continuing to product maturity. Our organization coordinates all aspects of production of Roche medicines in all disease areas... ...stability efforts to support early and late stage clinical studies, commercial launch and significant post-market modifications....Empfohlen
- ...implementation of modern and innovative trial/experimental designs, statistical models, analysis and data exploration methodologies at the study or project level and you will be responsible for all statistical work, scientific and operational, in collaboration with the...Empfohlen
- ...with internal and external partners to ensure scientific rigor in study design and analysis. Build partnerships with medical... ...methodologies, statistical methods, and observational/epidemiological studies. Proven track record in leading RWD research projects, including...Empfohlen
- ...seek successful registration and market access. This includes all medical and scientific aspects of clinical trials, programs and studies from the design phase, through implementation and finalization to include scientific and medical input into the final review and sign...EmpfohlenTemporär
- ...über Nebenwirkungen, Aufsicht über die Sicherheit in klinischen Studien und Post-Marketing-Programmen. Beteiligt sich an der Lösung... ...Safety Review Board (MSRB) Review and advise on mechanistic studies, Risk Management Plans, and safety signal action plans Contribute...EmpfohlenPostdoc Stelle
- ...investigators, and clinical site staff by addressing emergent needs Contributing to the delivery of the PD portfolio of clinical studies and programs across Disease Areas by providing operational and/or strategic input to the teams in the Clinical Operations Disease...Empfohlen
- ...Evidence (RWE). You will proactively identify evidence gaps that HTA bodies and payers have post-launch and design innovative RWE studies to address them. You will work in a highly collaborative, global environment to ensure these insights support the ongoing value of...Empfohlen
- ...experiments. About the Role Your responsibilities will include: Designing, conducting and protocolling independently in vivo studies with specific focus on neuroinflammatory pathways Establishment of new in vivo models for neuroinflammatory/neurodegenerative...Empfohlen
- ...vitro models. You will play a pivotal role in advancing the study of transport and permeability properties of new drug candidates... ...engaging with cross-functional teams to discuss results and coordinate studies conducted internally and with external partners. You maintain...EmpfohlenTemporär
- ...(including IEPs), BD&L assessments, asset maximization and indication sequencing Identify evidence, in addition to registration studies, required to meet the needs of medical experts and institutions involved in reimbursement & access decisions for key geographies....Empfohlen
- ...experience. ~ Significant experience and expertise in evidence generation activities, such as interventional or non-interventional studies and RWE projects. ~ Significant experience and expertise in the full range of medical affairs tactics with a deep understanding...Empfohlen
- ...features of real patient data while maintaining the privacy of the patients. Use causal networks to estimate the similarities between studies and other data sources. These other sources will help enrich smaller datasets and improve statistical robustness and predictions....
- ...Abfüllung von sterilen Darreichungsformen aus dem globalen Forschungs- und Entwicklungsportfolio. Für die Belieferung der klinischen Studien in Phase I–III stehen am Standort Basel „State of the art“ Fertigungsanlagen in einem modernen Gebäude zur Verfügung. Als “...
- ...Conduct quality control analyses of radioligands (e.g., HPLC, TLC, SEC) and ensure their readiness for preclinical in vitro and in vivo studies. Collaborative research: Collaborate effectively with multidisciplinary teams, including organic chemists, pharmacologists and...VollzeitLehrstelleFlexible Arbeitszeit
- ...review of trial data with Clinical Scientific Expert(s). May be the Program Manager of other associates (e.g.., CSE). May function as study medical monitor Support SR/GPCH in ensuring overall safety of the molecule. May be a core member of the Safety Management Team (...Invalidenversicherung
- ...instruments. Maintain and update the instrument database within the GMP management system. Oversee GMP instrument activities and coordinate updates to the validation master plan. Provide guidance on instrument-related problems, deviations, and compliance issues....
