4471 institute for clinical pharmacology & safety English-speaking jobs in Switzerland

Provide support for dose selection, study design and other clinical pharmacology matters throughout the ... clinical monitoring and integrated safety data review during and after the live phase of a study. ... 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. ... (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

Funded PhD position available to explore molecular mechanisms controlling immune-cell differentiation and function, focusing on human T cells.

The Director Non‑Clinical Due Diligence & External Evaluations provides scientific leadership for nonclinical ... The role ensures integrated, objective, and decision‑relevant evaluations of nonclinical pharmacology ... Integrate input from Toxicology, PK/QSP, Nonclinical Pharmacology, and external experts into a single ... Committee" Qualifications Education Advanced degree (Ph.D., D.V.M., or equivalent) in toxicology, pharmacology ... Trusted subject‑matter lead for nonclinical DD on individual deals.

Pharmacology, DMPK, Toxicology, Biomarkers, and Clinical Operations Support translational strategy and ... For our global Technical Operations Organization, we are currently looking for a Director, Analytical ... This position ensures robust, compliant, and innovative analytical approaches across preclinical, clinical ... queries Maintain inspection readiness and quality standards Cross‑Functional Collaboration Partner with Clinical ... The Director, Analytical Strategy is a senior scientific and strategic leadership role responsible for

end responsibility for all medical safety activities within clinical safety and pharmacovigilance in ... GCSP, you will be accountable for all medical safety related aspects of clinical safety and pharmacovigilance ... an experienced Head of Medical Safety GCSP providing medical leadership across Global Clinical Safety ... are available/developedEnsure high quality clinical safety contributions to development programs and ... signal management and risk minimizationYou bring solid knowledge of global clinical safety and pharmacovigilance

Development Safety Update Report, Periodic Safety Update Report, clinical benefit-risk assessment) o ... from Medical Affairs, Clinical Science, Regulatory, Safety/PV, non-clinical/PK, Biostatistics/Data management ... strategic guidance and being the ultimate accountable for: Clinical trial design (clinical study synopsis ... Provision of required input on clinical efficacy, safety, dosing/administration, mechanism of action, ... driving and representing the clinical development strategy for the nephrology program within the Core

of cross‑functional project teams, providing medicinal chemistry expertise and guidance to biology, pharmacology ... For our portfolio company SERAC Biosciences AG, we are looking for a motivated and experienced medicinal ... At Serac, this person will help drive projects from idea to clinical candidate while working closely ... medicinal chemistry, with a proven track record of advancing drug discovery programs from target ID to clinical ... Actively contribute to Serac’s medicinal chemistry effort, advancing projects from early discovery through clinical

Provide clinical judgment and analysis for case information and safety data. ... Solid understanding of global clinical trial and post‑marketing safety regulations. ... Collaborate with cross‑functional teams, including Safety, Clinical Development, Medical Affairs, and ... for pharmaceutical products in the cardiovascular space. ... Please note that to be considered for this role you must have the right to work in this location or hold

This roster is established for Individual Contractors (non-regular staff) to provide remote technical

This roster is established for Individual Contractors (non-regular staff) to support remote geospatial

This roster is established for Individual Contractors (non-regular staff) to contribute to the production

This roster is established for Individual Contractors (non-regular staff) to provide independent technical

Ensure consistency in safety data collection standards for clinical studies. ... Contribute to the development of safety-related sections in clinical protocols, Investigator's Brochures ... Conduct safety signal detection and benefit-risk assessments for assigned products. ... Lead global safety strategy for program teams, ensuring data-driven review and assessment. ... Experience in signal detection, evaluation, and aggregate data analysis in clinical trials.

PhD Position in Vehicle Sensor and Remote Sensing Analysis for Road Safety 100%, Zurich, fixed-term ... Adey within the Institute of Construction and Infrastructure Management of the Department of Civil, Enviromental ... referees) - Grades of all university courses taken as well as diplomas Further information about the Institute ... urban transport infrastructure safety analysis. ... for pedestrians, cyclists, and micromobility users.

It ensures that all products meet the highest clinical safety standards and comply with global regulatory ... Familiarity with basic laboratory techniques and safety protocols. ... Our Benefits For more information on CSL benefits visit How CSL Supports Your Well-being | CSL. ... Researches and develops innovative medicines to address unmet medical needs, from early discovery through clinical ... If you are an individual with a disability and need a reasonable accommodation for any part of the application

both clinical trial and post-marketing cases Prioritize and process safety cases in accordance with ... SAE reconciliation activities between clinical and safety databases Coordinate SUSAR notifications ... including triage, data entry, medical coding, narrative writing, quality review, and expedited reporting for ... We are committed to fostering respect, fairness, and equal opportunities for all job applicants and our ... For those partners who have no valid, signed Master Service Agreement in place with Idorsia, all unsolicited

both clinical trial and post-marketing cases - Prioritize and process safety cases in accordance with ... - Support SAE reconciliation activities between clinical and safety databases - Coordinate SUSAR notifications ... employees.*** Please be informed that if you are selected for this position, your employment will be ... including triage, data entry, medical coding, narrative writing, quality review, and expedited reporting for ... We are committed to fostering respect, fairness, and equal opportunities for all job applicants and our

safety surveillance activities.Lead global safety strategy for program teams, ensuring data‑driven review ... clinical studies.Oversee the preparation and submission of high‑quality safety reports.Conduct medical ... to the development of safety‑related sections in clinical protocols, Investigator's Brochures, informed ... and responses to health authority queries.Ensure consistency in safety data collection standards for ... and assessment.Conduct safety signal detection and benefit‑risk assessments for assigned products.Represent

decisions across global research and development teamsEssential RequirementsDoctor of Philosophy in Pharmacology ... studies across oncology programsCollaborate with cross‑functional teams to advance drug candidates toward clinical ... If, because of a medical condition or disability, you need a reasonable accommodation for any part of ... strategy, and translating complex data into meaningful insights that accelerate life‑changing therapies for ... The final level and title for this position will be determined following the completion of the candidate