4346 institute for clinical pharmacology & safety English-speaking jobs in Switzerland

Define appropriate strategies for clinical pharmacology/translational medicine, clinical PK, PK/PD, exposure-response ... Job Description Key Responsibilities Overall accountability for quantitative clinical pharmacology strategies ... Responsible for clinical pharmacology sections in regulatory documents and at interactions with regulatory ... Provide expert knowledge on clinical pharmacology and communicate clinical pharmacology aspects internally ... Represent clinical pharmacology on project Core Teams.

For our Clinical Pharmacology & Pharmacometrics Unit organization based at our Headquarters in Lausanne ... pharmacology strategy for assigned projects in Oncology or Infectious diseases · Manage the clinical ... the clinical pharmacology scientific strategy for assigned projects in Oncology and/or Infectious diseases ... , we are looking for a Principal Clinical Pharmacologist In this role, you will be the leader for developing ... pharmacology activities of assigned projects, by contributing to the design of clinical pharmacology

Pharmacology findings._ Your Contributions (include, but are not limited to): Develops Clinical Pharmacology ... Provides small and/or large molecule clinical pharmacology expertise to cross-functional project teams ... development, clinical pharmacology, and other development issues Contributes to training and mentoring ... (*in collaboration with AbbVie) About the Role: Develops overall Clinical Pharmacology scientific strategies ... and support for the preparation of regulatory submissions Develops new innovative and impactful clinical

studies across multiple programs, Develop innovative and meaningful clinical pharmacology approaches ... pharmacology strategy across a high volume of First-in-Human (FIH) and early clinical programs, as well ... clinical pharmacology at life cycle meetings Lead scientific discussions and provide strategic input ... Key Responsibilities Lead the design and execution of clinical pharmacology strategies and corresponding ... (CROs, modeling vendors) Qualifications & Experience PhD, PharmD, MD, or equivalent in Clinical Pharmacology

modelling services for the preclinical and clinical development of drugs to our customers worldwide. ... modelling services for the preclinical and clinical development of drugs to our customers worldwide. ... preclinical and clinical bio-therapeutics Understanding of drug discovery and development processes ... human diseases:LYO-X is the right place for you. ... modelling services dedicated to the preclinical and clinical development of biologics and cell-based

Closely interface with project team leaders as well as safety, clinical pharmacology, clinical operations ... leader, you will work within a matrix environment where influencing and inspiring others to strive for ... or clinical trials. ... clinical development. ... The Opportunity In this role, you will lead and/or support early‐stage clinical projects from entry into

General Responsibilities Responsible for clinical monitoring and integrated safety data review during ... Provide support for dose selection, study design, and other clinical pharmacology matters throughout ... pharmacology and profiling packages that meet regulatory requirements and support differentiated and ... Lead BR‑sub‑team(s) on Global Project Teams for late‑phase programs. ... Late‑Stage Clinical Projects (post‑TDP, “Profiling”) – In collaboration with the dermatology TA Head,

General responsibilities: Responsible for clinical monitoring and integrated safety data review during ... Provide support for dose selection, study design and other clinical pharmacology matters throughout the ... pharmacology and profiling packages that meet regulatory requirements and support differentiated and ... Innovation: Seeks out new clinical discovery opportunities and approaches to reach TDP. ... Drive success of late global programs by developing and implementing strategies that lead to clinical

You will assist the researchers on diverse tasks related to molecular and cellular biology as well as pharmacology ... EPFL, the Swiss Federal Institute of Technology in Lausanne, is one of the Technician EPFL, the Swiss ... Federal Institute of Technology in Lausanne, is one of the most dynamic university campuses in Europe

You have a background in animal or veterinary science, pharmacology, toxicology, biology, bioinformatics ... strong research network involving Agroscope, Empa (Dübendorf, Switzerland), and the German Federal Institute ... in ruminants Communication and publication of results in scientific journals, scientific reporting for ... for Risk Assessment (BfR, Berlin), offering an interdisciplinary and applied research environment at ... the interface of environmental science, animal science, and food safety.

The Swiss Cancer Institute is the national network for clinical cancer research in Switzerland. ... Guided by our vision "Clinical research for a cure tomorrow," we conduct oncology clinical trials and ... science or AI for clinical research either from industry (Development, Medical Affairs) or from academia ... You will shape and implement the scientific strategy of the institute, foster innovation and collaboration ... across cancer types, build and expand national and international research collaborations, represent the institute

The group is located at the Institute of Research for Biomedicine (IRB) in Bellinzona, Switzerland. ... The institute comprises a highly dynamic research environment focusing on studies of human disease, in ... particular for infections, inflammatory and degenerative diseases as well as cancer. ... While they are important for the induction of protective adaptive immunity against pathogens, they also ... Who we are looking for: – MSc or equivalent in immunology or other related backgrounds. – High level

General responsibilities: - Responsible for clinical monitoring and integrated safety data review during ... Provide support for dose selection, study design and other clinical pharmacology matters throughout the ... pharmacology and profiling packages that meet regulatory requirements and support differentiated and ... About the Role Key Responsibilities: Early clinical projects (Phase I / II, -Discovery-): Develop, ... Late-stage clinical projects (post-TDP, -Profiling-): In collaboration with the dermatology TA Head:

Director / Portfolio Safety Scientist Background For the Portfolio Clinical Safety team in Basel, we ... are looking for an experienced Associate Safety Director / Portfolio Safety Scientist to support safety ... Take responsibility for specialised PCS roles, such as subject expert, business process owner or safety ... Act independently as the safety representative within study teams and clinical safety-related activities ... Department: PDS/CSC/PCS - Portfolio Clinical Safety Basel Tasks and Responsibilities Develop and maintain

an experienced Head of Medical Safety GCSP providing medical leadership across Global Clinical Safety ... aspects of clinical safety and pharmacovigilance as well as ad hoc safety issues and innovation projects ... safety activities within clinical safety and pharmacovigilance in a science driven organization with ... **The role** As our Head of Medical Safety GCSP, you will be accountable for all medical safety related ... and skillsets are available/developed* Ensure high quality clinical safety contributions to development

decisions across global research and development teams Essential Requirements Doctor of Philosophy in Pharmacology ... If, because of a medical condition or disability, you need a reasonable accommodation for any part of ... Skills Desired Analytical Skill Analytical Thinking Chemical Biology Chemistry Clinical Research ... Clinical Trials Collaboration Communication Skills Curious Mindset Data Data Analysis Decision ... strategy, and translating complex data into meaningful insights that accelerate life‑changing therapies for

to identifying opportunities for innovation pipeline, based on clinical need, business opportunity, ... Desired Qualifications - PhD in biomedical sciences, bioengineering, pharmacology, physiology, or a related ... with R&D, Clinical, Regulatory and CRO, as well as academic partners. - Analyze and interpret pre-clinical ... Pre-clinical research - Support pre-clinical study planning, design, execution and reporting, in collaboration ... The company recently completed a major financing round which enables the expansion of the clinical program

Lead medical safety oversight for assigned clinical development programs Drive signal detection, evaluation ... safety, or clinical development Strong expertise in drug safety regulations, GCP, and global PV requirements ... Proven ability to interpret complex clinical safety data and drive decisions Experience with regulatory ... , and risk management strategies Act as chair and medical lead for the Safety Management Team (SMT) Present ... reporting About Your Skills & Experience For this role, we’re looking for a candidate who has an effective

Acts independently to manage safety responsibilities on study teams and in activities supporting clinical ... Contribute to the strategy and review of safety assessments and drug safety reports for signals or issues ... Responsible for the preparation and maintenance of safety sections of the Company Core Data Sheet and ... Take responsibility for safety science contributions to regulatory authority submissions (Investigational ... Review of clinical protocols, study reports, Investigator's Brochure (IB), informed consent form (ICF

end responsibility for all medical safety activities within clinical safety and pharmacovigilance in ... Clinical Safety & Pharmacovigilance (GCSP). ... of clinical safety and pharmacovigilance as well as ad hoc safety issues and innovation projects in ... The roleAs our Head of Medical Safety GCSP, you will be accountable for all medical safety related aspects ... are available/developed Ensure high quality clinical safety contributions to development programs and