relevant to your skills and experience. Design, plan and perform scientific experiments/plant activities and plan, perform and contribute to project related scientific/ technical activities under minimal
Deutschkenntnisse Planer
Design, plan and perform scientific experiments/plant activities and plan, perform and contribute to project related scientific/ technical activities under minimal guidance from more experienced team
mode of action, and safety aspects of the projects Plan and discuss the experimental strategy with the stakeholders, team members and data scientists Drive the execution of the experimental plans with
und Kontrollieren der bestehenden HLK-Pläne Koordinieren und Kontrollieren der ausführenden Gewerke Termin- und Qualitätskontrolle der Ausführung Dokumentation des Bauablaufs Verantwortung der Inbetriebnahme
emergent analytical methodologies, tools and applications to ensure fit-for-purpose and impactful approaches Produce high quality analyses: apply rigor in study design and analytical methods; plan for data
emergent analytical methodologies, tools and applications to ensure fit-for-purpose and impactful approaches Produce high quality analyses: apply rigor in study design and analytical methods; plan for data
relevant to your skills and experience. Design, plan and perform scientific experiments/plant activities and plan, perform and contribute to project related scientific/ technical activities under minimal
, planning and execution of the Medical Education activities and ensuring that these are based on insights and educational needs Plan and drive the publication activities, e.g. submissions to peer reviewed
implements mitigation plans at the study LevelReview of study data, discrepancy management and data cleaning BA/BS degree or equivalentModerate industry-related experience Moderate practical and theoretical
clinical teams Developing disease area strategies Developing clinical development, biomarker plans clinical protocols Closely interfacing with pharmacology, drug discovery and biomarker groups Leading and
Lesen und Kontrollieren der bestehenden HLK-Pläne Koordinieren und Kontrollieren der ausführenden Gewerke Termin- und Qualitätskontrolle der Ausführung Dokumentation des Bauablaufs Verantwortung
and Regulatory compliance Create GCP-compliant documentation for clinical projects (e.g., study plans, alidation reports, and study reports) Responsible for compliance with Safety, Health and
relevant to your skills and experience. Plan, organize, perform and document scientific experiments under moderate supervision; utilize special equipment or specialized facilities under moderate supervision
operational plans including, risk mitigation strategies, study budgets, sponsor capabilities (if applicable), and clinical supplies management Responsible to identify and update operational tracking tools
needs and is delivered according to plan Conduct stakeholder analysis, create and publish the related communication material (including training) and conduct information and communication sessions as well
Coordinate and oversee all aspects of outsourced safety studies, including communication to study directors at the CRO, study plan finalization, scientific monitoring during study conduct and report
relevant to your skills and experience. Develop operational plans including site monitoring strategies, risk mitigation strategies, trial budgets, site selection, and clinical supplies management Build
/-in FH/ETH mit Master oder Bachelor Solide Berufserfahrung im Tiefbau-/Bahnbaubereich Sehr gute Sprachkenntnisse in Deutsch (verhandlungssicher) Planer
aspects of the projects Plan and discuss the experimental strategy with the stakeholders, team members and data scientists Drive the execution of the experimental plans with constant inspection of the
disease area strategies Developing clinical development, biomarker plans clinical protocols Closely interfacing with pharmacology, drug discovery and biomarker groups Leading and supervising the
applications to ensure fit-for-purpose and impactful approaches Produce high quality analyses: apply rigor in study design and analytical methods; plan for data processing; design a fit-for-purpose analysis
applications to ensure fit-for-purpose and impactful approaches Produce high quality analyses: apply rigor in study design and analytical methods; plan for data processing; design a fit-for-purpose analysis
coordination of cross-functional tasksIdentify and escalates study issues appropriately and addresses corrective action plansEvaluate the impact of risks, and develops and implements mitigation plans at the
and ensuring that these are based on insights and educational needs Plan and drive the publication activities, e.g. submissions to peer reviewed journals scientific and medical education activities at
Plan, organize, perform and document scientific experiments under moderate supervision; utilize special equipment or specialized facilities under moderate supervision Work according to appropriate
Develop operational plans including site monitoring strategies, risk mitigation strategies, trial budgets, site selection, and clinical supplies management Build effective and efficient high
aspects of outsourced safety studies, including communication to study directors at the CRO, study plan finalization, scientific monitoring during study conduct and report finalization Ensure excellent
and the project team to ensure that the final solution meets the business requirements and customer’s needs and is delivered according to plan Conduct stakeholder analysis, create and publish the
Take the initiative, launch new projects, and lead activities within PDMA Medical Alliances Operations and the IIS / ISR / FMI-PHC Community of Practices Develop operational plans including, risk
Regulatory compliance Create GCP-compliant documentation for clinical projects (e.g., study plans, alidation reports, and study reports) Responsible for compliance with Safety, Health and Environment