Data operations manager állás, munka

The independent analyses of secondary data, including insurance claims, electronic medical record, patient survey, and disease registry....

PHARMACOEPIDEMIOLOGIST (M/F/D)- RWD/ EPIDEMIOLOGICAL/ PHARMACOEPIDEMIOLOGIC/ CLINICAL TRAILS/ BIOMARKER/ INSURANCE CLAIMS/ EHR/ MEDICAL/ MEDDRA/ SNOMED/ ICD 10/ CPT/ HCPCS/ R/ PYTHON/ SQL/ DATA VISUALIZATIONS/ R SHINY/ R MARKDOWM/ STATISTICAL ANALYSIS/ ENGLISH PROJECT: For our customer a big...

The Department of Translational Medical Oncology investigates the molecular and cellular mechanisms for cancer development, proliferation, and evolution. To strengthen our expertise in bioinformatics and machine learning, we are offering a position for a highly motivated scientist with significant...

PHARMACOEPIDEMIOLOGIST (M/F/D)- RWD/ EPIDEMIOLOGICAL/ PHARMACOEPIDEMIOLOGIC/ CLINICAL TRAILS/ BIOMARKER/ INSURANCE CLAIMS/ EHR/ MEDICAL/ MEDDRA/ SNOMED/ ICD 10/ CPT/ HCPCS/ R/ PYTHON/ SQL/ DATA VISUALIZATIONS/ R SHINY/ R MARKDOWM/ STATISTICAL ANALYSIS/ ENGLISH PROJECT: For our customer a big...

• A degree in Public Health, Epidemiology, Outcomes Research, Health Economics or a related scientific field; MSc or PhD in Epidemiology preferred
• Minimum 2 years of hands-on experience with Real World Data, non-interventional study design and analysis

Subject-Matter Expert (SME) for Test Method Development of delivery devices and combination products: Test Method development, including best practices for universal implementation, Test Method Validation/Transfer....

define medical communication and messaging concepts for assigned therapeutic areas based on customer insights, medical developments, and competitive monitoring in relevant markets, including consideration of trends in patient care...

• Coordination of the (partial) project to establish and continuously expand the EU reference network with all participating centres and clinics at EU level
• Participation in the helpdesk for the network's eHealth service
• Work with the project management team on the progression of the clinical registry

lead the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and company standards...

• Design, develop, and optimize coagulation diagnostic assays and reagents
• Lead feasibility studies, verification, and validation activities in compliance with ISOand IVDR requirements
• Document all activities according to quality system procedures and design control standards