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Principal Quantitative Scientist(m/w/x)
Leading advanced RWD studies for IVD, medical device, digital health decision support software. 7+ years related experience, RWD regulatory submission track record required. 5 weeks vacation, Apple hardware provided.
Requirements
- PhD (preferred) or Master’s Degree in Quantitative science field (e.g., Pharmacoepidemiology, Epidemiology, RWD Biostatistics, Pharmacoeconomics, Health Economic and Outcomes Research)
- 7+ years of directly related experience (industry, consulting, or relevant)
- Proven track record utilizing RWD for regulatory submissions
- Solid expertise in epidemiology and causal inference methodologies
- Strong experience using diverse RWD sources for insights and evidence
- Highly preferred experience in CVRM therapeutic area
- Proven hands-on experience designing, implementing, and reporting RWD studies
- Specific expertise in epidemiology
- Passion for making a difference in healthcare
- Programming experience with R, Python, SQL, or other quantitative software
- Solid understanding of regulatory guidelines
- Ability to use RWD to influence reimbursement and clinical guidelines
- Strong project management skills
- Ability to manage scope and delegate
- Recognized team leader experience
- Experience mentoring team members
- Resilient, can-do attitude
- Excellent communication and collaboration skills
- Ability to influence others without formal authority
- Professional working proficiency in English
- Data-savvy, creative, resilient problem solver
- Sense of ownership
- Attention to detail
- Eagerness to learn and expand scientific expertise
- Reliability as a team player and thought partner
Tasks
- Lead advanced RWD studies using healthcare databases.
- Develop rigorous RWD study protocols.
- Lead complex analyses for IVD, medical device, digital health.
- Ensure RWE meets highest scientific and methodological standards.
- Lead RWD projects for commercial, market access, regulatory needs.
- Champion RWD to supplement clinical evidence.
- Identify RWD opportunities for regulatory and reimbursement.
- Collaborate with external partners on study design.
- Foster relationships to explore new data and methods.
- Expand expertise in RWD, epidemiology, and causal inference.
- Promote innovation by enhancing processes, methods, technology.
- Share learnings proactively with peers.
- Mentor junior colleagues.
- Act as an influential subject matter expert.
Work Experience
- 7 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- R
- Python
- SQL
Benefits
Flexible Working
- Flexible working hours
- Home office policy
Modern Equipment
- Apple hardware
Healthcare & Fitness
- Fitness
- Healthy lifestyle
Public Transport Subsidies
- Public transport
Free or Subsidized Food
- Lunch benefit
Learning & Development
- Language classes
- Professional training budget
Career Advancement
- Global conferences opportunity
Family Support
- Family friendly career paths
Sustainability Focus
- Sustainability
Modern Office
- Flexible modern workplace
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Principal Quantitative Scientist(m/w/x)
Leading advanced RWD studies for IVD, medical device, digital health decision support software. 7+ years related experience, RWD regulatory submission track record required. 5 weeks vacation, Apple hardware provided.
Requirements
- PhD (preferred) or Master’s Degree in Quantitative science field (e.g., Pharmacoepidemiology, Epidemiology, RWD Biostatistics, Pharmacoeconomics, Health Economic and Outcomes Research)
- 7+ years of directly related experience (industry, consulting, or relevant)
- Proven track record utilizing RWD for regulatory submissions
- Solid expertise in epidemiology and causal inference methodologies
- Strong experience using diverse RWD sources for insights and evidence
- Highly preferred experience in CVRM therapeutic area
- Proven hands-on experience designing, implementing, and reporting RWD studies
- Specific expertise in epidemiology
- Passion for making a difference in healthcare
- Programming experience with R, Python, SQL, or other quantitative software
- Solid understanding of regulatory guidelines
- Ability to use RWD to influence reimbursement and clinical guidelines
- Strong project management skills
- Ability to manage scope and delegate
- Recognized team leader experience
- Experience mentoring team members
- Resilient, can-do attitude
- Excellent communication and collaboration skills
- Ability to influence others without formal authority
- Professional working proficiency in English
- Data-savvy, creative, resilient problem solver
- Sense of ownership
- Attention to detail
- Eagerness to learn and expand scientific expertise
- Reliability as a team player and thought partner
Tasks
- Lead advanced RWD studies using healthcare databases.
- Develop rigorous RWD study protocols.
- Lead complex analyses for IVD, medical device, digital health.
- Ensure RWE meets highest scientific and methodological standards.
- Lead RWD projects for commercial, market access, regulatory needs.
- Champion RWD to supplement clinical evidence.
- Identify RWD opportunities for regulatory and reimbursement.
- Collaborate with external partners on study design.
- Foster relationships to explore new data and methods.
- Expand expertise in RWD, epidemiology, and causal inference.
- Promote innovation by enhancing processes, methods, technology.
- Share learnings proactively with peers.
- Mentor junior colleagues.
- Act as an influential subject matter expert.
Work Experience
- 7 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- R
- Python
- SQL
Benefits
Flexible Working
- Flexible working hours
- Home office policy
Modern Equipment
- Apple hardware
Healthcare & Fitness
- Fitness
- Healthy lifestyle
Public Transport Subsidies
- Public transport
Free or Subsidized Food
- Lunch benefit
Learning & Development
- Language classes
- Professional training budget
Career Advancement
- Global conferences opportunity
Family Support
- Family friendly career paths
Sustainability Focus
- Sustainability
Modern Office
- Flexible modern workplace
About the Company
mySugr GmbH
Industry
Healthcare
Description
The company is committed to transforming healthcare through sustainable action and innovation, focusing on early diagnosis and targeted treatments.
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