Truveta Inc.
Truveta is the world’s first health provider-led data platform with a vision of Saving Lives with Data. Our mission is to enable researchers to find cures faster, empower every clinician to be an expert, and help families make the most informed decisions about their care. Achieving Truveta’s ambitious vision requires an incredible team of talented and inspired people with a special combination of health, software, and big data experience who share our company values.
Truveta was born in the Pacific Northwest, but we have employees who live across the country. Our team enjoys the flexibility of a hybrid model and working from anywhere. In person attendance is required for two weeks during the year for Truveta Planning Weeks.
For overall team productivity, we optimize meeting hours in the Pacific time zone. We avoid scheduling recurring meetings that start after 3pm PT; however, ad hoc meetings occur between 8am-6pm Pacific time.
#LI-remote
Who We Need Truveta is rapidly building a talented and diverse team to tackle complex health and technical challenges. We seek problem solvers, passionate and collaborative teammates, and those willing to roll up their sleeves while making a difference. If you are interested in purposeful work, joining a mission-driven team, and building a rewarding career while having fun, Truveta may be the perfect fit for you.
This Opportunity We are seeking a Senior Research Epidemiologist to join the Partner Research and Success team. This role focuses on supporting strategic research engagements with our Life Sciences partners, leading the design, development, and implementation of customer-driven research on the Truveta Platform and with our Healthcare Member Systems. The ideal candidate will have experience with regulatory submissions, strong analytical skills, and healthcare data expertise, and will collaborate with clients to fulfill their research needs.
Pharmacoepidemiological experience is highly preferred.
Key Qualifications Mandatory:
Master's degree in Epidemiology or a related field with 7+ years of epidemiology experience, or a PhD in Epidemiology or related field with 3+ years of experience.
5+ years of hands-on statistical programming experience with R and/or Python.
5+ years of experience developing and executing statistical analysis plans in a research setting.
3+ years analyzing Electronic Health Record data or other Real World Data sources in healthcare.
Experience responding to regulatory requests from US, European, or other agencies related to risk management, safety studies, and reporting.
Ability to lead development of SOWs and SAPs for regulatory submissions.
Familiarity with Good Pharmacoepidemiology Practices (GPP) and ENCEPP.
Proven ability to collaborate with clients on research needs.
Experience with peer-review publication process and leading submissions.
Excellent written and verbal communication skills.
Experience working in a startup environment.
Preferred:
Pharmacoepidemiology and pharmacovigilance focus.
3+ years experience with SAS and SQL.
Why Truveta? Join us to build something special. We offer strong leadership, funding, a culture that values people and passions, and opportunities for growth. Be part of building an innovative company.
We Offer:
Meaningful work at every career stage.
Comprehensive benefits including medical, dental, vision, 401K, and parental leave.
Professional development and training opportunities.
Flexible work hours and paid time off.
Generous parental leave.
Team activities (virtual and in-person when possible).
Base salary range: $142,000-$180,000, based on experience and location. Additional incentives may apply.
We encourage California residents to review
important information here .
Truveta values diversity and inclusion, welcoming applicants from all backgrounds, especially those historically excluded from tech roles. We encourage individuals with diverse identities to apply.
Note: All applicants must be authorized to work in the US. We cannot sponsor visas at this time.
#J-18808-Ljbffr
Truveta was born in the Pacific Northwest, but we have employees who live across the country. Our team enjoys the flexibility of a hybrid model and working from anywhere. In person attendance is required for two weeks during the year for Truveta Planning Weeks.
For overall team productivity, we optimize meeting hours in the Pacific time zone. We avoid scheduling recurring meetings that start after 3pm PT; however, ad hoc meetings occur between 8am-6pm Pacific time.
#LI-remote
Who We Need Truveta is rapidly building a talented and diverse team to tackle complex health and technical challenges. We seek problem solvers, passionate and collaborative teammates, and those willing to roll up their sleeves while making a difference. If you are interested in purposeful work, joining a mission-driven team, and building a rewarding career while having fun, Truveta may be the perfect fit for you.
This Opportunity We are seeking a Senior Research Epidemiologist to join the Partner Research and Success team. This role focuses on supporting strategic research engagements with our Life Sciences partners, leading the design, development, and implementation of customer-driven research on the Truveta Platform and with our Healthcare Member Systems. The ideal candidate will have experience with regulatory submissions, strong analytical skills, and healthcare data expertise, and will collaborate with clients to fulfill their research needs.
Pharmacoepidemiological experience is highly preferred.
Key Qualifications Mandatory:
Master's degree in Epidemiology or a related field with 7+ years of epidemiology experience, or a PhD in Epidemiology or related field with 3+ years of experience.
5+ years of hands-on statistical programming experience with R and/or Python.
5+ years of experience developing and executing statistical analysis plans in a research setting.
3+ years analyzing Electronic Health Record data or other Real World Data sources in healthcare.
Experience responding to regulatory requests from US, European, or other agencies related to risk management, safety studies, and reporting.
Ability to lead development of SOWs and SAPs for regulatory submissions.
Familiarity with Good Pharmacoepidemiology Practices (GPP) and ENCEPP.
Proven ability to collaborate with clients on research needs.
Experience with peer-review publication process and leading submissions.
Excellent written and verbal communication skills.
Experience working in a startup environment.
Preferred:
Pharmacoepidemiology and pharmacovigilance focus.
3+ years experience with SAS and SQL.
Why Truveta? Join us to build something special. We offer strong leadership, funding, a culture that values people and passions, and opportunities for growth. Be part of building an innovative company.
We Offer:
Meaningful work at every career stage.
Comprehensive benefits including medical, dental, vision, 401K, and parental leave.
Professional development and training opportunities.
Flexible work hours and paid time off.
Generous parental leave.
Team activities (virtual and in-person when possible).
Base salary range: $142,000-$180,000, based on experience and location. Additional incentives may apply.
We encourage California residents to review
important information here .
Truveta values diversity and inclusion, welcoming applicants from all backgrounds, especially those historically excluded from tech roles. We encourage individuals with diverse identities to apply.
Note: All applicants must be authorized to work in the US. We cannot sponsor visas at this time.
#J-18808-Ljbffr