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Principal Quantitative Scientist(m/w/x)
Advanced RWD study design and execution using diverse databases for patient care decision software. Proven RWD regulatory submission track record and causal inference expertise required. 5 weeks vacation, Apple hardware.
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 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
- Hands-on experience designing, implementing, reporting RWD studies; specific epidemiology expertise; passion for healthcare
- Programming experience with R, Python, SQL, or other quantitative software
- Solid understanding of regulatory guidelines; ability to use RWD to influence reimbursement/clinical guidelines
- Strong project management skills (scope management, delegation); recognized team leader; experience mentoring team members; resilient, can-do attitude
- Excellent communication and collaboration skills; ability to influence without formal authority; professional working proficiency in English
- Data-savvy, creative, resilient problem solver; sense of ownership; attention to detail; eagerness to learn; reliable team player; thought partner
Tasks
- Conceptualize advanced RWD studies
- Plan advanced RWD studies
- Execute advanced RWD studies using diverse databases
- Report on advanced RWD study findings
- Develop rigorous RWD study protocols
- Lead complex analyses for portfolio evidence needs
- Ensure RWE meets high scientific and methodological standards
- Lead RWD initiatives with cross-functional teams
- Ensure RWD projects meet 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 methodologies
- Expand expertise in RWD, epidemiology, and causal inference
- Enhance processes, methods, and technology for innovation
- Share learnings 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
- RWD
- R
- Python
- SQL
Benefits
Flexible Working
- Flexible working hours
- Home office policy
Modern Equipment
- Apple hardware
Healthcare & Fitness
- Fitness
Public Transport Subsidies
- Public transport
Free or Subsidized Food
- Lunch benefit
Learning & Development
- Language classes
- Professional training budget
Career Advancement
- Global conferences opportunity
Modern Office
- Amazing office
Startup Environment
- Rooftop terrace
Snacks & Drinks
- Fully stocked kitchen
- Barista coffee machines
Not a perfect match?
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Principal Quantitative Scientist(m/w/x)
Advanced RWD study design and execution using diverse databases for patient care decision software. Proven RWD regulatory submission track record and causal inference expertise required. 5 weeks vacation, Apple hardware.
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 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
- Hands-on experience designing, implementing, reporting RWD studies; specific epidemiology expertise; passion for healthcare
- Programming experience with R, Python, SQL, or other quantitative software
- Solid understanding of regulatory guidelines; ability to use RWD to influence reimbursement/clinical guidelines
- Strong project management skills (scope management, delegation); recognized team leader; experience mentoring team members; resilient, can-do attitude
- Excellent communication and collaboration skills; ability to influence without formal authority; professional working proficiency in English
- Data-savvy, creative, resilient problem solver; sense of ownership; attention to detail; eagerness to learn; reliable team player; thought partner
Tasks
- Conceptualize advanced RWD studies
- Plan advanced RWD studies
- Execute advanced RWD studies using diverse databases
- Report on advanced RWD study findings
- Develop rigorous RWD study protocols
- Lead complex analyses for portfolio evidence needs
- Ensure RWE meets high scientific and methodological standards
- Lead RWD initiatives with cross-functional teams
- Ensure RWD projects meet 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 methodologies
- Expand expertise in RWD, epidemiology, and causal inference
- Enhance processes, methods, and technology for innovation
- Share learnings 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
- RWD
- R
- Python
- SQL
Benefits
Flexible Working
- Flexible working hours
- Home office policy
Modern Equipment
- Apple hardware
Healthcare & Fitness
- Fitness
Public Transport Subsidies
- Public transport
Free or Subsidized Food
- Lunch benefit
Learning & Development
- Language classes
- Professional training budget
Career Advancement
- Global conferences opportunity
Modern Office
- Amazing office
Startup Environment
- Rooftop terrace
Snacks & Drinks
- Fully stocked kitchen
- Barista coffee machines
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.
Not a perfect match?
- RHI Magnesita GmbH
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Quantitative Research Analyst(m/w/x)
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Senior Machine Learning Engineer(m/w/x)
Full-time/Part-timeWith HomeofficeSeniorWienfrom 52,136 / year - mySugr GmbH
Design Operations Lead(m/w/x)
Full-timeWith HomeofficeSeniorWienfrom 3,843 / month