Clinical Study Analyst (m/f/d)

Your tasksLead GCP-Compliant Clinical Diagnostic Studies: Design, implement, and manage diagnostic accuracy studies in compliance with ICH-GCP and regulatory standards, ensuring data integrity, patient safety, and ethical conduct.Project Management Excellence: Plan, allocate resources, schedule, and oversee all aspects of the project, including protocol development, ethics approvals, study site management, and data collection, to ensure timely and high-quality execution.Data Oversight, Analysis and Scientific Contribution: Build research networks, analyze clinical and diagnostic data, and lead and contribute to peer-reviewed publications, reports, and scientific presentations.Budget and Timeline Management: Monitor study and project progress against milestones, ensuring delivery within scope, timelines, and budget constraints while maintaining transparent communication with stakeholders and funder.Stakeholder and Team Leadership: Foster collaboration among investigators, study sites, partners, and other stakeholders to drive program success and advance diagnostic technology initiatives.Your profilePostgraduate training in a relevant field (e.g., Biomedical Science, Epidemiology) with at least 2 years’ experience in planning, execution, and oversight of GCP-compliant diagnostic accuracy studies; experience in diagnostic development is an advantage;Strong skills in planning, resource allocation, scheduling, and progress monitoring to manage projects effectively from inception to completion;In-depth understanding of infectious diseases, particularly lower respiratory tract infection, and related public health issues, diagnostic tools, and trends in the field;Data analysis skills and ability to use statistical software for data management and analysis (e.g. R, Stata)Excellent interpersonal, writing, and presentation skills to coordinate teams, engage with stakeholders, and disseminate research findings to both technical and non-technical audiences; and,Proven track record of contributing to peer-reviewed publications, reports, and presentations to effectively communicate project findings to advance diagnostic innovation and public health impact.Your tasksLead GCP-Compliant Clinical Diagnostic Studies: Design, implement, and manage diagnostic accuracy studies in compliance with ICH-GCP and regulatory standards, ensuring data integrity, patient safety, and ethical conduct.Project Management Excellence: Plan, allocate resources, schedule, and oversee all aspects of the project, including protocol development, ethics approvals, study site management, and data collection, to ensure timely and high-quality execution.Data Oversight, Analysis and Scientific Contribution: Build research networks, analyze clinical and diagnostic data, and lead and contribute to peer-reviewed publications, reports, and scientific presentations.Budget and Timeline Management: Monitor study and project progress against milestones, ensuring delivery within scope, timelines, and budget constraints while maintaining transparent communication with stakeholders and funder.Stakeholder and Team Leadership: Foster collaboration among investigators, study sites, partners, and other stakeholders to drive program success and advance diagnostic technology initiatives.Your tasksLead GCP-Compliant Clinical Diagnostic Studies: Design, implement, and manage diagnostic accuracy studies in compliance with ICH-GCP and regulatory standards, ensuring data integrity, patient safety, and ethical conduct.Project Management Excellence: Plan, allocate resources, schedule, and oversee all aspects of the project, including protocol development, ethics approvals, study site management, and data collection, to ensure timely and high-quality execution.Data Oversight, Analysis and Scientific Contribution: Build research networks, analyze clinical and diagnostic data, and lead and contribute to peer-reviewed publications, reports, and scientific presentations.Budget and Timeline Management: Monitor study and project progress against milestones, ensuring delivery within scope, timelines, and budget constraints while maintaining transparent communication with stakeholders and funder.Stakeholder and Team Leadership: Foster collaboration among investigators, study sites, partners, and other stakeholders to drive program success and advance diagnostic technology initiatives.Lead GCP-Compliant Clinical Diagnostic Studies: Design, implement, and manage diagnostic accuracy studies in compliance with ICH-GCP and regulatory standards, ensuring data integrity, patient safety, and ethical conduct.Project Management Excellence: Plan, allocate resources, schedule, and oversee all aspects of the project, including protocol development, ethics approvals, study site management, and data collection, to ensure timely and high-quality execution.Data Oversight, Analysis and Scientific Contribution: Build research networks, analyze clinical and diagnostic data, and lead and contribute to peer-reviewed publications, reports, and scientific presentations.Budget and Timeline Management: Monitor study and project progress against milestones, ensuring delivery within scope, timelines, and budget constraints while maintaining transparent communication with stakeholders and funder.Stakeholder and Team Leadership: Foster collaboration among investigators, study sites, partners, and other stakeholders to drive program success and advance diagnostic technology initiatives.Your profilePostgraduate training in a relevant field (e.g., Biomedical Science, Epidemiology) with at least 2 years’ experience in planning, execution, and oversight of GCP-compliant diagnostic accuracy studies; experience in diagnostic development is an advantage;Strong skills in planning, resource allocation, scheduling, and progress monitoring to manage projects effectively from inception to completion;In-depth understanding of infectious diseases, particularly lower respiratory tract infection, and related public health issues, diagnostic tools, and trends in the field;Data analysis skills and ability to use statistical software for data management and analysis (e.g. R, Stata)Excellent interpersonal, writing, and presentation skills to coordinate teams, engage with stakeholders, and disseminate research findings to both technical and non-technical audiences; and,Proven track record of contributing to peer-reviewed publications, reports, and presentations to effectively communicate project findings to advance diagnostic innovation and public health impact.Postgraduate training in a relevant field (e.g., Biomedical Science, Epidemiology) with at least 2 years’ experience in planning, execution, and oversight of GCP-compliant diagnostic accuracy studies; experience in diagnostic development is an advantage;Strong skills in planning, resource allocation, scheduling, and progress monitoring to manage projects effectively from inception to completion;In-depth understanding of infectious diseases, particularly lower respiratory tract infection, and related public health issues, diagnostic tools, and trends in the field;Data analysis skills and ability to use statistical software for data management and analysis (e.g. R, Stata)Excellent interpersonal, writing, and presentation skills to coordinate teams, engage with stakeholders, and disseminate research findings to both technical and non-technical audiences; and,Proven track record of contributing to peer-reviewed publications, reports, and presentations to effectively communicate project findings to advance diagnostic innovation and public health impact.What we offerCollectively agreed remuneration TV-L E13, attractive company pension scheme (VBL)30 days vacationSustainable travel: job ticketFamily-friendly working environment: cooperative arrangements for childcare, subsidy for child vacation care, advice for employees with relatives in need of careWide range of health, prevention and sports offersWhat we offerCollectively agreed remuneration TV-L E13, attractive company pension scheme (VBL)30 days vacationSustainable travel: job ticketFamily-friendly working environment: cooperative arrangements for childcare, subsidy for child vacation care, advice for employees with relatives in need of careWide range of health, prevention and sports offersCollectively agreed remuneration TV-L E13, attractive company pension scheme (VBL)30 days vacationSustainable travel: job ticketFamily-friendly working environment: cooperative arrangements for childcare, subsidy for child vacation care, advice for employees with relatives in need of careWide range of health, prevention and sports offersContact & ApplicationInterested?Applications will be accepted until 15.12.2025 in our online portal. Emailed applications will not be considered.Infektions- und TropenmedizinDr. Ankur Gupta-WrightIm Neuenheimer Feld 32469120 HeidelbergInterested?Applications will be accepted until 15.12.2025 in our online portal. Emailed applications will not be considered.Infektions- und TropenmedizinDr. Ankur Gupta-WrightIm Neuenheimer Feld 32469120 Heidelberg