Boehringer Ingelheim
ROPu RWE Manager(m/w/x)
Full-timeWith HomeofficeExperienced
Wien
from 83,250 / year
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MYmySugr GmbH
Principal Quantitative Scientist(m/w/x)
Wien
from 3,843 / month
Full-timeWith Home OfficeSenior
Nejo AI Summary
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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of mySugr GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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MYmySugr GmbH
Principal Quantitative Scientist(m/w/x)
Wien
from 3,843 / month
Full-timeWith Home OfficeSenior
Nejo AI Summary
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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of mySugr GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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?
- Boehringer Ingelheim
ROPu RWE Manager(m/w/x)
Full-timeWith HomeofficeExperiencedWienfrom 83,250 / year - mySugr GmbH
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Full-timeFreelanceWith HomeofficeExperiencedWien - Körber Pharma Austria GmbH
Statistics & Modelling Consultant(m/w/x)
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Python Software Engineer - Scientific Computing(m/w/x)
Full-timeWith HomeofficeExperiencedWienfrom 40,000 / year - mySugr GmbH
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Full-timeFreelanceWith HomeofficeExperiencedWien