33 Jobs für Pharmacology Expert
Stellenangebote Pharmacology Expert Jobs
Job vor 3 Tagen bei Jobleads gefunden
[. .. ] creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam DAngelo, Larry Summers, and Jack [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Dorsey. Position: Medical Expert Type: Contractor Compensation: 80100/ hour Location: Remote Commitment: 3040 hours/ week Role Responsibilities Review and audit AI-generated medical content, including clinical explanations, differential diagnoses, treatment recommendations, research summaries, and patient-facing materials. Evaluate medical text quality using structured rubrics (810 criteria) , focusing on accuracy, evidence alignment, clarity, and [. .. ] Verify correctness of clinical reasoning, identifying logical gaps, unsafe recommendations, or unsupported claims. Assess adherence to medical guidelines, best practices, and standard terminology. Identify errors related to medical facts, pathophysiology, pharmacology, contraindications, or misinterpretation of clinical data. Provide clear, concise written feedback to justify evaluation decisions. Work independently and asynchronously using provided tools and workflows. Qualifications Must-Have Advanced medical training (MD, DO, RN, PA, NP, clinical researcher, or equivalent background) . Strong understanding of clinical reasoning, diagnostic process, and evidence-[. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Junior/ Senior/ Principal Scientist-Systems Pharma/ Toxicology (PBPK-QSP/ T)
• Niedersachsen
Absolventen, Einsteiger, Trainees Homeoffice möglich
[. .. ] and motivated life-science modelling simulation scientist with experience in the pharma industry? Do you enjoy driving innovation and setting new boundaries in physiologically-based (PBPK) modelling, pharmacokinetics, quantitative [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] systems pharmacology and toxicology (QSP/ T) ? This position offers you this and more exciting work in an innovative and fast-paced environment. ES Qlabs is an innovative, internationally acting Contract Research Organization and a global leader in the development and application of the OSP Suite (www. open-systems-pharmacology. org) . [. .. ] submitting, and receiving approval for publications in scientific journals Mechanistic physiologically based pharmacokinetic modeling and simulation experience Proficiency in a scripting language for modeling and simulation (ideally R, alternatively MATLAB) Expert knowledge in domain-specific modeling software (e. g. PK-Sim/Mo Bi, Sim Cyp, or Gastro Plus, Simbiology, SBML/ Tellurium/Antimony) Excellent communication, presentation, and leadership skills Relationship-building skills with the ability to work closely with project leaders and team members Strong organization skills and ability to handle multiple [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] business. Undertake major business development efforts successfully with little or no assistance. Identify and pursue new business opportunities, develop and convert proposals, and lead thought leadership activities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as subject matter expert to enhance the firms market presence. Help to recruit, develop, and mentor team members, fostering a collaborative and inclusive culture and ensuring knowledge transfer across the practice. Provide hands on development experience for team members as their supervisor. Qualifications (English) Ph. D. in life sciences (e. g. , biology, biotechnology, biochemistry, pharmacology etc. ) or MBA, with 7+ years relevant postdegree professional experience (consulting experience preferred) . Alternately, a Bachelors or Masters degree in a life sciences, business, economics or related discipline, with 9+ years relevant postdegree professional experience (consulting experience preferred) . Proven team and project leadership skills, including project planning, [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Senior Scientific Expert Neurotoxin (m/f/d)
• Frankfurt, Hesse
YOUR CONTRIBUTION Join our motivated team as Senior Scientific
Expert Neurotoxin (m/f/d) and contribute to advancing our scientific expertise in the field of neurotoxins. In this role, you will serve [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as the scientific interface between the Global Nonclinical Lab, Pilot Plant, and production, leading method transfer and development activities, and safeguarding the marketability and regulatory requirements of our [. .. ] neurology and propose new indications for botulinum toxin, including coordination of feasibility studies and contribution to IP generation. YOUR PROFILE Ph D (or equivalent) in Life Sciences (e. g. , biochemistry, pharmacology) with strong expertise in protein biochemistry and analytics, ideally focused on neurotoxin analytics. Handson experience with method development/ transfer, CMC/ analytical support, and crossfunctional coordination in a GMP environment. Experience in pharmaceutical drug development with solid understanding of endtoend processes is a plus. Excellent English skills (written and spoken) . [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Principal (Life Sciences practice)
• München, Bayern
[. .. ] business. Undertake major business development efforts successfully with little or no assistance. Identify and pursue new business opportunities, develop and convert proposals, and lead thought leadership activities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as subject matter expert to enhance the firms market presence. Help recruit, develop, and mentor team members, fostering a collaborative and inclusive culture and ensuring knowledge transfer across the practice. Provide handson development experience for team members as their supervisor. Qualifications: Ph. D. in life sciences (e. g. , biology, biotechnology, biochemistry, pharmacology etc. ) or MBA, with 7+ years relevant postdegree professional experience (consulting experience preferred) . Alternately, a Bachelors or Masters degree in a life sciences, business, economics or related discipline, with 9+ years relevant postdegree professional experience (consulting experience preferred) . Proven team and project leadership skills, including project planning [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Senior Clinical Project Pharmacologist
• Basel, Basel- Stadt
[. .. ] listed on the SIX Swiss Exchange (ticker symbol: IDIA) . We are excited to invite a talented and experienced Senior Clinical Pharmacologist to join our dynamic team. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As a functional expert within a small, innovative group, you will play a pivotal role in advancing our clinical development programs. In this highly collaborative environment, you will provide strategic guidance on pharmacokinetics (PK) , pharmacodynamics (PD) , and drug interactions to ensure the successful progression of our drug pipeline. Job Responsibilities Lead and manage design and conduct of clinical pharmacology studies of increasing complexity, ensuring study deliverables are met on time, on budget, and with appropriate quality. Interpret, report, and present study results to Life Cycle Teams, Development Teams, and committees comprising members of Idorsia Senior Leadership. Provide expertise to the PK/ PD section of protocols for phase IIb IV studies. [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• Zürich
[. .. ] The Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] leads the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. The role is responsible for the design, adequate budgeting, and monitoring of nonclinical safety studies conducted internally and externally in both a GLP and non GLP environment. Regulatory Toxicology Role: The Principal Toxicologist will compile Toxicological [. .. ] with clinical development plans. Proactively identify and manage safety risks and liabilities early in development across therapeutic modalities. Prepare and review regulatory nonclinical submission documents. Collaborate with internal stakeholders including pharmacology, PK, clinical, regulatory, and CMC teams. Present integrated safety assessments to senior management and at project milestone reviews. Compile toxicological risk assessments for impurities, extractables and leachables, excipients, and other components in line with ICH, EMA, and FDA guidelines. Stay current with evolving toxicology guidelines and risk assessment methodologies. Qualifications [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Executive Director, Oncology Early Clinical Development Lead
• Zug
Führungs-/ Leitungspositionen
[. .. ] Clinical Matrix Team, providing clinical leadership, Oncology expertise, and customer insight. Oversee translational science strategy execution in partnership with Oncology Early Development Leaders, Translated Science, preclinical research, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] AI/ ML, Clinical Pharmacology, and Experimental Medicine. Partner with Oncology Tumor Teams (OTTs) to develop translational strategy across assets and drive OTT activities with a clinical focus. Capture complex translational and clinical data, identify trends, and consult on safety analyses and regulatory queries. Prepare abstracts, presentations, and manuscripts for accuracy and compliance. Lead preparation [. .. ] maintain relationships with key external experts, academic collaborators, and external research organizations. Collaborate with Principal Investigators and Steering Committees to evaluate publications linked to clinical data. Serve as program medical expert for internal and external collaborators, investigators, and consultants. Lead, coach, and mentor a team of Oncology Early Clinical Development Medical Directors and Clinical Scientists, conducting regular staff meetings, checkins, and 1:1 meetings. Ensure crossfunctional integration, coordination, and alignment for effective CDP and translational strategy execution. Foster a culture of boldness, [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
• Morges, Waadt
Führungs-/ Leitungspositionen
[. .. ] human (ph 1 or 2) . Participates in asset/ portfolio strategies and prioritization, internal and external messaging, governance, and cross-functional interface with all key stakeholders, including translational [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] science, clinical pharmacology and pharmacometrics, discovery organization, regulatory and others. Provides medical and scientific expertise for internal cross-functional team members for development of specific, hematology-oncology agents including discovery scientists, clinical scientists, biostatisticians, pharmacokinetics, pharmacovigilance, and clinical operations. Supports interactions with global regulatory bodies including the FDA, EMA, PMDA and TGA and [. .. ] development of anticancer agents. Provides guidance for successful implementation and accomplishment of investigator-initiated trials related to product development and life cycle management of a compound. Acts as subject matter expert for business development activities Professional Competencies Business Insights MD, MD-Ph D. Hematology-oncology board certification is preferred. Training in research (wet lab) , proven track record of self-directed scientific work (e. g. , post doc, peer reviewed publications as first author) preferred. Experience in early drug development required with [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
Clinical Evaluation Manager-Freelancer (m/f/d)
• Wien
Freiberuflich
[. .. ] activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatory-compliant Clinical Evaluation Reports (CERs) to demonstrate device safety and performance. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to post-market. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practises. Essential skills for your mission: Experience: + 1-3 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: + Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: + Strong analytical and problem-solving skills + Excellent written and verbal communication skills in English + Detail-oriented with the ability to manage multiple tasks and deadlines + Capability to make risk-based decisions Technical Proficiency: + Basic [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] their consulting career path by recognizing and seeking opportunities that match their ambition and personal interests. Responsibilities Support projects for Certaras clients by working in teams with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] other Associates, senior expert modelers, and drug development consultants. Hands-on pharmacometric modeling on client projects as a billable consultant. Conduct quality control activities on model codes and reports. May lead/coordinate company initiatives (e. g. IT, methodology, efficiency, automation, quality) . May act as the primary point of contact for clients and collaborate with a senior consultant to grow business to match their interests. Qualifications Ph D, MD, Pharm D in Bioengineering, Pharmaceutical Sciences, Pharmacology, Statistics, Applied Mathematics, Engineering, Medicine, or related field. 1 to 5 years of industry/ consulting experience working in R D, pre-clinical and clinical environments (may be combined with academic research) . Solid experience in pharmacometrics, clinical pharmacology, pharmacokinetics, or a related discipline in a project team setting is preferred, [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
Clinical Evaluation Manager-Freelancer (m/f/d)
• Wien
Freiberuflich
[. .. ] activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatory-compliant Clinical Evaluation Reports (CERs) to demonstrate device safety and performance. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to post-market. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practices. Essential skills for your mission: Experience: 13 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: Strong analytical and problemsolving skills; Excellent written and verbal communication skills in English; Detailoriented with the ability to manage multiple tasks and deadlines; Capability to make riskbased decisions Technical Proficiency: Basic understanding of clinical research and biostatistics; Proficiency in [. .. ]
Job am 22.11.2025 bei Jobleads gefunden
• Opfikon, Zürich
Führungs-/ Leitungspositionen
Overview The Senior Director of Nonclinical Toxicology Pharmacokinetics is responsible for overseeing the strategic direction, execution, and integration of nonclinical safety, pharmacokinetics (PK) , and advanced modelingincluding Quantitative Systems
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>Pharmacology (QSP) to support drug development from discovery through clinical stages across all Therapeutic Areas. This role ensures that all Toxicology and Pharmacokinetic data support regulatory submissions and clinical development and thereby enable effective FIH transition and provide data-driven insights to inform decision-making. Strategic Leadership Lead the nonclinical safety [. .. ] Ensure compliance with GLP and ICH guidelines for nonclinical studies. Cross-functional Collaboration Collaborate with relevant R D functions to align Tox/ PK insights and strategies with development goals. Provide
expert input into due diligence for in-licensing or partnership opportunities. Collaborate with External Study Management for study execution at CROs. Present findings at internal meetings, scientific conferences, and in peer-reviewed publications. Team Leadership Build and mentor a multidisciplinary team of toxicologists, pharmacokineticists, and modelers. Foster a culture of scientific [. .. ]
▶ Zur Stellenanzeige
Job am 22.11.2025 bei Jobleads gefunden
Director Translational Sciences (Oncology)
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Jobticket
[. .. ] deep knowledge of and extensive experience with oncology, the role will drive the translational strategies for clinical development of oncology programs based on an integrated view of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the respective translational expert functions Responsible for bridging preclinical experimental data to translational strategies in the assigned programs to deeply integrate the mechanism of action to the clinical development plan (target engagement, pharmacodynamics endpoints, patient selection) and correlate with clinical outcomes The role will provide scientific, technologic and strategic guidance and handson contribution to [. .. ] and solve complex problems, experience in collaborating with external specialty laboratories Experience in working within interdisciplinary crossfunctional teams with other key development functions (clinical lead, regulatory, biostatistics, operations and clinical pharmacology) to develop and execute the biomarker strategy in alignment with clinical development objectives Ability to independently drive, manage, execute, and deliver results for a portfolio of complex multifunctional projects Eagerness to work in the dynamic environment of a fastgrowing company and comfortable in working in a matrix environment (global/ crossfunctional) [. .. ]
Job am 22.11.2025 bei Jobleads gefunden
• Glattbrugg, Zürich
Führungs-/ Leitungspositionen
[. .. ] Description Summary The PK/ QSP Lead is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK) , toxicokinetic (TK) , physiologically-based pharmacokinetic (PBPK) , and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] quantitative systems pharmacology (QSP) modeling strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas. Main Responsibilities Strategic Leadership Scientific Expertise Lead the development and execution of integrated PK, PBPK, and QSP modeling strategies across multiple therapeutic programs. Serve as the subject matter expert (SME) in modeling and simulation, advising project teams on optimal study design, dose selection, and risk assessment. Champion model-informed drug development (MIDD) approaches to enhance translational understanding and regulatory confidence. PK and Model Development Lead the design and execution of nonclinical PK and TK studies to support research and [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
Director, Non-clinical Pharmacology CVR
• Schlieren, Zürich
Führungs-/ Leitungspositionen
[. .. ] dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. We are seeking a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Therapeutic Area (TA) Pharmacology Lead (Transplant Immunology) to drive the design, execution, and interpretation of in vivo pharmacology studies that support drug discovery and development. This role is pivotal in characterising the pharmacological profile of novel therapeutic candidates through internal studies and external collaborations. Main Responsibilities Scientific Leadership Define and lead the nonclinical pharmacology [. .. ] Sr. Pharmacology lead on TA teams. Work closely with PK, Toxicology, Translational Science, to integrate pharmacology data into broader development plans. Participate in project teams and TA-teams and provide expert input on pharmacology-related issues. Provide expert input into due diligence for in-licensing or partnership opportunities. Documentation Communication Prepare study reports, presentations, and regulatory documents (e. g. , IND, CTA) . Present findings to internal stakeholders and external collaborators as needed. Team Leadership Lead and mentor a team of [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Toxicology
• Zürich
[. .. ] Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lead the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. The role is responsible for the design, adequate budgeting, and monitoring of non-clinical safety studies conducted internally and externally both in a GLP and non-GLP environment Regulatory Toxicology Role: The Principal Toxicologist will [. .. ] with clinical development plans. Proactively identify and manage safety risks and liabilities early in development across therapeutic modalities Prepare and review regulatory nonclinical submission documents Collaborate with internal stakeholders including pharmacology, PK, clinical, regulatory, and CMC teams. Present integrated safety assessments to senior management and at project milestone reviews. Compile toxicological risk assessments for impurities, extractables and leachables, excipients, and other components in line with ICH, EMA, and FDA guidelines Stay current with evolving toxicology guidelines and risk assessment methodologies. Qualifications [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Regulatory Toxicology
• Glattbrugg, Zürich
[. .. ] The Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. The role serves as the primary toxicology representative on interdisciplinary project teams, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] leads the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. Responsibilities include design, budgeting, and monitoring of nonclinical safety studies in GLP and non GLP environments. The role also compiles toxicological risk assessments across multiple projects, supporting R D, CMC and quality and/or compiling nonclinical [. .. ] with clinical development plans. Proactively identify and manage safety risks and liabilities early in development across therapeutic modalities. Prepare and review regulatory nonclinical submission documents. Collaborate with internal stakeholders including pharmacology, PK, clinical, regulatory, and CMC teams. Present integrated safety assessments to senior management and at project milestone reviews. Compile toxicological risk assessments for impurities, extractables and leachables, excipients, and other components in line with ICH, EMA, and FDA guidelines. Stay current with evolving toxicology guidelines and risk assessment methodologies. Qualifications [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Director Pharmacokinetics (PK) Quantitate Systems Pharmacology (QSP)
• Zürich
Führungs-/ Leitungspositionen
Director Pharmacokinetics (PK) Quantitate Systems
Pharmacology (QSP) page is loaded # # Director Pharmacokinetics (PK) Quantitate Systems Pharmacology (QSP) locations: EMEA, CH, Kanton Zurich, Opfikon, CSL Vifortime type: Vollzeitposted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on: Heute ausgeschriebenjob requisition id: R-263621CSLs R D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus [. .. ] multiple therapeutic areas. Main Responsibilities:Strategic Leadership Scientific Expertise Lead the development and execution of integrated PK, PBPK, and QSP modeling strategies across multiple therapeutic programs. Serve as the subject matter expert (SME) in modeling and simulation, advising project teams on optimal study design, dose selection, and risk assessment. Champion model-informed drug development (MIDD) approaches to enhance translational understanding and regulatory confidence. PK and Model Development Lead the design and execution of nonclinical PK and TK studies to support research and [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Regulatory Toxicology
• Zürich
[. .. ] Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lead the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. The role is responsible for the design, adequate budgeting, and monitoring of non-clinical safety studies conducted internally and externally both in a GLP and non-GLP environment Regulatory Toxicology Role: The Principal Toxicologist will [. .. ] with clinical development plans. Proactively identify and manage safety risks and liabilities early in development across therapeutic modalities Prepare and review regulatory nonclinical submission documents Collaborate with internal stakeholders including pharmacology, PK, clinical, regulatory, and CMC teams. Present integrated safety assessments to senior management and at project milestone reviews. Compile toxicological risk assessments for impurities, extractables and leachables, excipients, and other components in line with ICH, EMA, and FDA guidelines Stay current with evolving toxicology guidelines and risk assessment methodologies. Qualifications [. .. ]
Job am 31.10.2025 bei Jobleads gefunden
(Senior) Scientific Affairs Director Clinical Pharmacology (flexible location in EU)
Führungs-/ Leitungspositionen
[. .. ] our Client who are a top global drug development company with strong presence in Europe, we are looking for a (Sr) Director Scientific Affairs who will provide [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Scientific and Clinical Pharmacology expertise internally as well as externally. In this role you will: Serve as an expert in Clinical Pharmacology on feasibility requests, partnership/ preferred provider requests and medical safety committees Provide Scientific and Clinical Pharmacology input to proposals and lead protocol design activities for phase I/ IIa studies in clinical trials Represent the company in front of clients and acts as primary contact for business development [. .. ]
Job am 28.10.2025 bei Jobleads gefunden
Senior Clinical Project Pharmacologist
• Allschwil, Basel- Landschaft
[. .. ] on the SIX Swiss Exchange (ticker symbol : IDIA) . We are excited to invite a talented and experienced Senior Clinical Pharmacologist to join our dynamic team. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As a functional expert within a small, innovative group, you will play a pivotal role in advancing our clinical development programs. In this highly collaborative environment, you will provide strategic guidance on pharmacokinetics (PK) , pharmacodynamics (PD) , and drug interactions to ensure the successful progression of our drug pipeline. If you are passionate about making a meaningful impact and thrive in a hands-on, collaborative setting, wed love to hear from you. Job Responsibilities Leads and manages design and conduct of clinical pharmacology studies of increasing complexity, ensuring study deliverables are met on time, on budget, and with the appropriate quality Interprets, reports, and presents study results to Life Cycle Team, Development Team, and committees comprising members of Idorsia Senior Leadership Provides expertise to the PK/ PD section of protocol of phase llb-[. .. ]
Job am 04.10.2025 bei Jobleads gefunden
Clinical Pharmacology Leader
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Clinical
Pharmacology Leader page is loaded # # Clinical Pharmacology Leaderlocations: Basel: Welwyntime type: Tempo integralposted on: Publicado hojejob requisition id: 202509-124199At Roche you can show up as yourself, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted [. .. ] , formulation device development and special population studies (e. g. , renal impairment, hepatic impairment) . You contribute to clinical trial design (from Phase 1 to Phase 3) : provide expert input on clinical trial protocols, data analysis plans, and clinical study reports. Responsible and accountable for all dedicated clinical pharmacology studies. You act as a subject matter expert: serve as the primary clinical pharmacology representative on project teams, due diligence teams and at internal and external meetings (e. g. , [. .. ]
Job am 02.10.2025 bei Jobleads gefunden
Business Development Manager, UK Nordics, 100
• Schlieren, Zürich
[. .. ] experience. A minimum of 5 years of experience in life science related commercial activities in the UK is a must. The ideal candidate will be viewed as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a subject matter expert in the field and will work in close collaboration with our scientific leadership team, marketing team and key functional areas. This role will be based in the UK (remote) . YOUR RESPONSIBILITIES Devise a business plan to achieve regional targets Map out key accounts and create strategic plans for growth [. .. ] in the Customer Relationship Management database Maintain knowledge of competitive landscape and market trends and communicate changes to internal Biognosys teams YOUR PROFILE University Degree in life sciences, molecular biology, pharmacology, biochemistry, or related fields Commercial experience in life science, contract research services, human diagnostics or relevant field in the UK is a requirement Willingness to travel frequently for customer visits and conferences, with some travel to Biognosys headquarters in the Zurich area Strong interest in connecting scientific information with a [. .. ]
Job am 25.09.2025 bei Jobleads gefunden
Senior Director, Toxicology Pharmacokinetics
• Glattbrugg, Zürich
Führungs-/ Leitungspositionen
Overview Senior Director of Nonclinical Toxicology Pharmacokinetics is responsible for overseeing the strategic direction, execution, and integration of nonclinical safety, pharmacokinetics (PK) , and advanced modelingincluding Quantitative Systems
Pharmacology [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (QSP) to support drug development from discovery through clinical stages across all Therapeutic Areas. This role ensures that all Toxicology and PK data support regulatory submissions and clinical development and thereby enable effective FIH transition and provide data-driven insights to inform decision-making. Responsibilities Lead the nonclinical safety and [. .. ] NDAs, BLAs) . Ensure compliance with GLP and ICH guidelines for nonclinical studies. Collaborate with relevant R D functions to align Tox/ PK insights and strategies with development goals. Provide expert input into due diligence for in-licensing or partnership opportunities. Collaborate with External Study Management for study execution at CROs. Present findings at internal meetings, scientific conferences, and in peer-reviewed publications. Build and mentor a multidisciplinary team of toxicologists, pharmacokineticists, and modelers. Foster a culture of scientific excellence, innovation, [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmacology expert pro Jahr?
Als Pharmacology expert verdient man zwischen EUR 70.000,- bis EUR 100.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmacology Expert Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 33 offene Stellenanzeigen für Pharmacology Expert Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmacology Expert Jobs?
Aktuell suchen 5 Unternehmen nach Bewerbern für Pharmacology Expert Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmacology Expert Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmacology Expert Stellenangebote:
- Merz Therapeutics (1 Job)
- Charles River Associates (1 Job)
- Herman Medical Staffing GmbH (1 Job)
In welchen Bundesländern werden die meisten Pharmacology Expert Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacology Expert Jobs werden derzeit in Niedersachsen (7 Jobs), Berlin (3 Jobs) und Bayern (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacology Expert Jobs?
Pharmacology Expert Jobs gehören zum Berufsfeld Pharmazie.
