Associate Director, Clinical Outcomes Assessment - Quantitative Research - Digital Health R&D Oncology – Evinova
US - Gaithersburg - MD, United States
R
USD 151K-226K Mid-level Full Time
Tasks
- Advise on documentation reporting and data management for regulatory compliance
- Design and interpret data analyses
- Develop evidence strategy
- Develop patient centric endpoints
- Disseminate findings to regulators payers and healthcare professionals
- Ensure work complies with Good Laboratory Practice Safety Health and Environment and Animal Welfare
- Independently execute and interpret research studies and analytical work
- Perform data evaluation triage adverse event interpretation and anomaly recognition
- Provide quantitative measurement support for patient centered measurement strategy
- Select data collection strategy for clinical research and real world settings
- Support validation and review of protocols and methodologies
Perks/Benefits
Skills/Tech-stack
Adverse Event | Adverse event analysis | Change Management | Clinical Outcomes | Clinical outcomes assessment | Data Analysis | Data Capture | Data Management | EMA | Endpoint development | Event analysis | Evidence Strategy | FDA | Good Laboratory Practice | Health related quality of life | Laboratory practice | Outcomes Research | Outcomes assessment | Patient reported outcomes | Psychometrics | Regulatory Compliance | Research study design | Safety Health and Environment | Sensor Data Analysis | Sensor data | Study design | Wearable Data Capture | Wearable data
Education
Bachelor of Science | Doctor of Public Health | Master of Public Health | Master of Science | PhD
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