360 institute for clinical pharmacology & safety English-speaking jobs in Canton of Basel-Stadt

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.

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

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

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

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

We are looking for candidates with strong expertise in in vitro and/or in vivo pharmacology, a solid ... in the area of metabolic diseases (insulin resistance, obesity) from target ideation to entry into clinical ... opportunityIn this role, you will design and execute experiments and lead projects to evaluate the efficacy and safety ... At Roche you can show up as yourself, embraced for the unique qualities you bring. ... how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for

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

, competitor safety data, and mechanisms of action Lead medical reviews for individual case safety reports ... Director level and proven track record GxP & clinical trial lifecycle expertise At least 4 years of ... regulatory inquiries Drive signal detection, assessment, and management, including strategy development for ... Company Core Data Sheet, labeling documents, risk communications, and Risk Management Plans Review clinical ... safety evaluations and drug safety reports Independently own risk management activities: develop and

Conduct signal detection and management, contributing to safety assessments and reports for regulatory ... Familiarity with GxP standards and the clinical trial lifecycle. ... Please note that to be considered for this role you must have the right to work in this location or hold ... Review clinical protocols, study reports, Investigator Brochures (IB), and informed consent forms (ICF ... Prepare and maintain safety sections of the Company Core Data Sheet and Reference Safety Information.

Team, overseeing medical safety monitoring and contributing to PSURs, clinical overviews, and risk management ... GMA‐led clinical research activities - Jointly review and approve clinical activities led by Clinical ... , safety oversight, and regulatory requirements - Proven experience engaging Key Opinion Leaders and ... and patients Collaboration, Safety & Compliance - Build and sustain strong collaboration with regional ... and national label changes, including safety‐related updates - Ensure that all medical and promotional

Team, overseeing medical safety monitoring and contributing to PSURs, clinical overviews, and risk management ... GMA‑led clinical research activities Jointly review and approve clinical activities led by Clinical ... and patients Collaboration, Safety & Compliance Build and sustain strong collaboration with regional ... and national label changes, including safety‑related updates Ensure that all medical and promotional ... relationships with Key Opinion Leaders and scientific societies Act as a core member of the Product Safety

Provide clinical insight into patient safety, data review, and overall study conduct. ... The Director of Clinical Development is accountable for leading and supporting the clinical development ... RhyGaze is an innovative, growing biotech company developing next-generation therapies for serious eye ... regulatory strategy, and key program milestones, with a focus on advancing innovative gene therapy programs for ... Benefits Why Join Us Opportunity to help develop breakthrough therapies for patients with serious vision‐threatening

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for ... Work closely with Market Access, Commercial, Regulatory, Safety, and Corporate Affairs teams to ensure ... Required Experience Act as the Medical Affairs lead for Switzerland, accountable for local medical ... regulations and clinical practice. ... the Country Manager Switzerland, the Medical Director, Switzerland is the medical leader responsible for

Jobdescription For our client, a dynamic international biotechnology company focused on clinical-stage ... Regional Strategy: Take responsibility for protocols to identify region-specific operational issues for ... CRO Management: Act as the medical monitor or provide oversight for CRO partners regarding medical queries ...  in Basel, Switzerland / Remote model Responsibilities: Lead Clinical Development: Provide clinical and ...  the territory and provide medical oversight of clinical projects where necessary.

The Strategic Feasibility Expert is accountable for the clinical feasibility strategy for Biomedical ... Areas and individual clinical trials. ... for you. ... Excellent understanding of the drug development process, preferably early clinical development. ... Collaborate with the Clinical Finance Manager on early strategic planning to provide input into site