At Target RWE, our mission is driven by a deep commitment to people, whether it’s the patients we serve, the partners we collaborate with, or the dedicated team members who power our work. As a purpose-driven organization, we leverage real-world data to advance clinical research and inform better healthcare decisions. We foster a collaborative environment where every voice is heard, every idea has an impact, and every contribution helps improve lives. If you're seeking a place where your work truly matters, join us to advance science.

Overview

We are seeking a Principal to join Target RWE’s Quantitative Sciences (QS) organization. In this role, you will help shape how we design, execute, and communicate real-world clinical studies using Target’s data.

This is a highly cross-functional and client-facing role. You will bring strong analytical and scientific expertise, paired with the ability to apply the right level of methodological rigor for the question at hand, balancing credibility, practicality, and clarity. You will work closely with internal teams and external partners to ensure analyses are scientifically sound, clearly communicated, and aligned with real-world use cases.

You will serve as a key representative of Target’s scientific capabilities, engaging directly with pharmaceutical and biotech partners, supporting client discussions, and helping translate complex analytical approaches into clear, actionable insights.

What You’ll Do

Applied Methodology and Study Design

You will ensure that Target’s analyses are scientifically rigorous, practical, and aligned with real-world use.

• Guide the design of observational studies using real-world data, including retrospective and prospective analyses
• Apply statistical and epidemiologic methods in a practical, fit-for-purpose way
• Develop and review study protocols and statistical analysis plans
• Ensure analyses are reproducible, interpretable, and aligned with regulatory and scientific expectations
• Partner with internal teams to translate research questions into practical analytic approaches

Client-Facing Scientific Leadership

You will serve as a key scientific voice in client and partner interactions.

• Participate in and lead client meetings to explain study design, methodology, and results
• Translate complex analytical concepts into clear, accessible language for diverse audiences
• Support business development efforts by helping communicate Target’s scientific approach and data value
• Represent Target in external settings, including conferences, scientific collaborations, and partner discussions
• Build trust with clients by providing thoughtful, pragmatic, and credible scientific guidance

Cross-Functional Collaboration

You will connect data, analytics, and business needs across the organization.

• Partner closely with Product, Engineering, Medical Science, Clinical Operations, and Commercial teams
• Help shape analytic strategies that align with both scientific goals and customer needs
• Provide guidance to the Quantitative Sciences team on study design and interpretation
• Mentor team members on balancing methodological rigor with practical execution
• Contribute to internal best practices for scalable, high-quality evidence generation

What You’ll Bring

• PhD or MS in biostatistics, epidemiology, health economics, data science, or a related field
• 10+ years of experience working with real-world data (EMR, claims, registry, or clinical trial data)
• Strong foundation in observational study design and applied statistical methods; experience with real-world pragmatic clinical trial designs is a plus
• Demonstrated ability to apply methods pragmatically, selecting the right approach for the problem
• Willingness to engage directly with data and analyses as needed, with working knowledge of R and/or SQL to support exploratory work, validation, and collaboration with analytic teams
• Experience working directly with clients or external partners in life sciences or healthcare
• Excellent communication and presentation skills, with the ability to explain complex concepts clearly
• Comfortable operating in client-facing settings, including meetings, presentations, and scientific discussions
• Strong collaboration skills across technical and non-technical teams

What we offer you

• Hybrid work — 3 days/week in our brand-new office!
• Comprehensive health, dental, and vision for you and your family
• 401(k) with company match
• Generous PTO and company holidays
• Paid parental leave 

About QuantHealth
QuantHealth (QH) is a rapidly growing company specializing in the development of a cutting-edge platform for simulating clinical trials using big clinical data and state-of-the-art AI technologies. Our mission is to provide innovative solutions to pharmaceutical and biotechnology companies for de-risking the drug and clinical development process. 
We are looking for a Pre-Sales individual contributor with strong expertise in both medical and data sciences to join our team, to support the company’s commercial efforts, working directly with pharma and biotech clients to help drive impactful collaborations. 

The Role
As a Pre-Sales, Data Science FAS Manager, you will serve as a technical and scientific ambassador for QuantHealth’s platform. You will work within Sales, and in tight collaboration with Product, and Data Science teams to articulate the value of our models, demonstrate our technology to prospects and customers, and support commercial engagements with deep technical credibility.
The annual salary for this role is $165,000 - $228,000, depending on experience, skills, and other relevant considerations. 

Responsibilities

• Act as a technical partner to Sales, supporting pre-sales and post-sales engagements 
• Lead platform demonstrations and technical walkthroughs 
• Explain and defend KG and RWD-driven models 
• Answer in-depth customer questions on data sources, modeling, and validation 
• Translate complex analytics into commercially relevant narratives 
• Collaborate with Product and Data Science teams 
• Provide customer feedback to inform roadmap and messaging 

Qualifications 

• Advanced degree (MS or PhD preferred) in a quantitative field 
• Deep hands-on data science experience (experience at consulting or pharma company highly preferred) 
• Experience with machine learning, statistical modeling, and real-world data 
• Commercially minded and customer-facing 
• Strong communication and presentation skills 
• Strong Preference for: biostatistician or epidemiologist with 3-7 yrs in pharma/biotech (sponsor-side or CRO), deep understanding of clinical trial design, endpoints, and regulatory submissions 

Who You Are 

• A hybrid thinker who enjoys both deep technical problem-solving and customer interaction 
• Comfortable leading scientific discussions with senior stakeholders 
• Naturally curious, pragmatic, and impact-driven 
• Confident explaining complex models without oversimplifying 
• Energized by supporting revenue-generating conversations 

What Success Looks Like in 30 Days 

• Confidently delivering end-to-end platform demos independently 
• Supporting live sales cycles with minimal ramp support 
• Clearly articulating QuantHealth’s modeling approach and value proposition 
• Building trust with Sales, Product, and Data Science teams 
• Contributing actionable feedback from customer conversations 

Senior Research Epidemiologist

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 at least once per year for an onsite meeting. 

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. Beyond core capabilities, we are seeking problem solvers, passionate and collaborative teammates, and those willing to roll up their sleeves while making a difference. If you are interested in the opportunity to pursue purposeful work, join a mission-driven team, and build a rewarding career while having fun, Truveta may be the perfect fit for you. 

This Opportunity  

We are seeking an experienced Senior Research Epidemiologist to lead and execute high-quality, client-driven epidemiological and health services research. This role is responsible for the end-to-end delivery of real-world evidence studies supporting life sciences, healthcare, and regulatory decision-making. The ideal candidate brings strong pharmacoepidemiology and/or regulatory-facing research experience. This is a highly collaborative, client-facing role that combines methodological leadership, project execution, and scientific communication. 

Key Responsibilities 

Research Leadership & Execution 

• Lead and execute end-to-end epidemiological and real-world evidence studies, ensuring scientific rigor, transparency, and regulatory relevance.
• Design and oversee study protocols, statistical analysis plans (SAPs), study reports, and manuscripts.
• Apply advanced epidemiologic methods across various study designs.
• Collaborate closely with analytics and data science teams to review results, assess robustness, and interpret findings.
• Stay current with evolving regulatory guidance, observational research methods, and industry standards. 

Project Management 

• Serve as a primary research point of contact for customers, including life sciences partners and regulatory-focused stakeholders.
• Manage project timelines, resources, deliverables, and risks across multiple concurrent studies.
• Clearly communicate study design, methodology, and findings to internal teams, clients, and external stakeholders.
• Build and maintain trusted relationships with customers seeking regulatory-grade real-world evidence. 

Qualifications & Experience

Required Qualifications

• Master’s or PhD in Epidemiology, Public Health, Biostatistics, Health Policy, or a related field.
• 7+ years of experience in epidemiological, pharmacoepidemiology, or health services research, including leadership or project management responsibilities.
• Demonstrated experience designing and executing observational studies using real-world data.
• Experience working with electronic health records (EHRs), claims data, or other real-world healthcare data sources.
• Proven ability to manage complex, client-facing projects and deliver high-quality outputs under tight timelines.
• Excellent written and verbal communication skills, including presenting technical concepts to diverse audiences. 

Highly Desired / Preferred Experience

• Hands-on experience with statistical programming (R and/or Python).
• Track record of peer-reviewed publications.
• Experience working in a startup or fast-paced, growth-oriented environment. 

Why Truveta?  

Be a part of building something special. Now is the perfect time to join Truveta. We have strong, established leadership with decades of success. We are well-funded. We are building a culture that prioritizes people and their passions across personal, professional and everything in between. Join us as we build an amazing company together.  

We Offer:

• Interesting and meaningful work for every career stage
• Great benefits package
• Comprehensive benefits with strong medical, dental and vision insurance plans
• 401K plan
• Professional development & training opportunities for continuous learning
• Work/life autonomy via flexible work hours and flexible paid time off
• Generous parental leave
• Regular team activities (virtual and in-person)
• The base pay for this position is $142,000-$180,000. The pay range reflects the minimum and maximum target. Pay is based on several factors including location and may vary depending on job-related knowledge, skills, and experience. Certain roles are eligible for additional compensation such as incentive pay and stock options.

If you are based in California, we encourage you to read this important information for California residents linked here.

Truveta is committed to creating a diverse, inclusive, and empowering workplace. We believe that having employees, interns, and contractors with diverse backgrounds enables Truveta to better meet our mission and serve patients and health communities around the world. We recognize that opportunities in technology historically excluded and continue to disproportionately exclude Black and Indigenous people, people of color, people from working class backgrounds, people with disabilities, and LGBTQIA+ people. We strongly encourage individuals with these identities to apply even if you don’t meet all of the requirements.

Please note that all applicants must be authorized to work in the United States for any employer as we are unable to sponsor work visas or permits (e.g. F-1 OPT, H1-B) at this time. We appreciate your interest in the position and encourage you to explore future opportunities with us.

LEAP Program Description

Global Solutions Ventures (GSV) – a joint-venture partnership between ZemiTek, LLC and Dexis Consulting Group – is implementing the Long-term Exceptional Technical Assistance Project (LEAP Global), a mechanism originally used by USAID to battle against infectious diseases such as malaria, HIV/AIDS, tuberculosis, neglected tropical diseases, and pandemic influenza. As of July 1, 2025, LEAP Global transitioned to the U.S. Department of State (DOS). This initiative aims to address the complex human resource challenges faced by national infectious disease programs in the USA-supported countries.

The intervention of this project is to hire and embed technical expert advisors and subject matter experts within government entities. By directly embedding the technical expertise within the national programs, LEAP provides long-term, sustainable lifesaving support to empower host governments to lead and manage key aspects of their infectious disease portfolios and improve coordination between the U.S. Government and the host country.

About the Position

The Outbreak Prevention and Response Officer- multisectoral coordination and community health systems will support Haiti’s effort to prevent, detect and respond to infectious disease threats, aligned with the US Department of State’s America First Global Health Strategy and Global Health security priorities in carrying out life-saving humanitarian assistance (LHA) service delivery in full alignment with the new Presidential Executive Order (EO) directives. The position will strengthen multisectoral collaboration and the integration of the polyvalent community health workers in surveillance, early warning, and community resilience

The role supports the assessment, design, coordination, and implementation of an integrated, inclusive, and operational approach to outbreak prevention, detection, and response aligned with national policies and the US priorities. The position supports implementation of evidence-based interventions consistent with the Multisectoral Health Framework approach.

Responsibilities

• Support the direction of health promotion and outbreak response of MSPP (DPSPE) to assess and strengthen outbreak prevention, and response capacities, community surveillance, and early warning systems, at departmental and community level, in line with Global Health security priorities.
• Contribute to the identification and prioritizations of high impact public health threats with potential regional or cross-border implications using data-driven and risk-based approaches.
• Support the development and implementation of practical, cost-effective strategies and actions plans for local outbreak prevention and response tools such as WASH-FIT, community-based surveillance, and health information systems.
• Lead the development of the national health promotion and evidence-based communication strategy.
• Strengthening multisectoral coordination among human health and animal health, local authorities, civil society, faith-based organization and private sector partners, consistent with the Multisectoral Health Framework and US government global health security objectives.
• Collaborate with CDC, national training institutions, to pave a way for the sustainability of the FETP program beyond U.S.G funding, graduates’ integrations in the national system and the public sector.
• Support the integration, training, and effective deployment of polyvalent community health workers and the field epidemiologist to enhance early detection, reporting, promotion, and community level response to outbreaks.
• Promote accountability, transparency, and result oriented programing using measurable indicators, monitoring and evaluation frameworks, and routine performance reporting.
• Facilitate stakeholder consultations, technical workshops, and validation processes, and support the dissemination of agreed strategies, tools and guidance.
• Contribute to evidence-based communication and community engagement efforts that promote preventive behaviors and strengthen trust in public health systems during outbreaks and health emergencies.

COMMUNICATIONS 

• Regular conference calls with multisectoral stakeholders, U.S. Embassy and GHSD Washington to review progress, discuss activities and address emerging issues. 
• The GHS Technical Advisor should provide information and avail him/herself for calls/meetings with the State Department/U.S. Embassy as requested. 
• The advisor will provide monthly reports to US Embassy/U.S. Department of State 

REPORTING: 

The Outbreak Prevention and Response Officer will provide a detailed monthly report to the U.S. Department of State at the end of each month. Additionally, the Advisor may be required to submit additional reports at the discretion of the U.S. Department of State and LEAP Global. The format for reporting may be adjusted with concurrence from the COR. 

Qualifications

• Advanced degree in medicine, infectious disease, public health, Epidemiology, Health Systems, veterinary medicine/animal health, or related field.
• Training in Field Epidemiology (FETP), infectious disease, Evidence-based Communication, or WASH/IPC preferred.
• 5–7 years of progressive experience in outbreak prevention/response, community health systems, or health security in LMIC settings, ideally in Haiti or the Caribbean.
• Demonstrated experience strengthening multi-sectoral coordination, CBS/EWS, and health promotion/Evidence-based communications at national.
• Hands-on experience working with CHWs and departmental health teams.
• Experience collaborating with MSPP, CDC, USG or similar.
• Experience in PEPFAR, PMI and other multilateral infectious disease and epidemic control programs.
• Verbal and written professional proficiency in English and French.

LEAP Program Description

Global Solutions Ventures (GSV) – a joint-venture partnership between ZemiTek, LLC and Dexis Consulting Group – is implementing the Long-term Exceptional Technical Assistance Project (LEAP Global), a mechanism originally used by USAID to battle against infectious diseases such as malaria, HIV/AIDS, tuberculosis, neglected tropical diseases, and pandemic influenza. As of July 1, 2025, LEAP Global transitioned to the U.S. Department of State (DOS). This initiative aims to address the complex human resource challenges faced by national infectious disease programs in the USA-supported countries.

The intervention of this project is to hire and embed technical expert advisors and subject matter experts within government entities. By directly embedding the technical expertise within the national programs, LEAP provides long-term, sustainable lifesaving support to empower host governments to lead and manage key aspects of their infectious disease portfolios and improve coordination between the U.S. Government and the host country.

About the Position

The Senior Global Health Security (GHS) Advisor will support the Papua New Guinea National Department of Health (NDOH) in coordinating, tracking, and implementing the Memorandum of Understanding (MOU) between the Government of the United States of America and the Government of the Independent State of Papua New Guinea.  This five-year MOU aims to strengthen PNG's health system, achieve HIV cascade targets, reduce maternal and child mortality, enhance infectious disease surveillance and outbreak response capabilities.  The Health Expert will provide technical leadership across four key areas of cooperation: (1) Surveillance & Outbreak Response, (2) Laboratory Systems, (3) Data Systems, and (4) Strategic Investment, while managing critical transitions including the transfer of U.S.-funded frontline healthcare workers and digital health systems to PNG Government management.

The Senior GHS Advisor will support the NDOH and relevant government departments through the GHS Multisectoral Steering Committee (MSC) and technical working groups for: (i) coordination and tracking of MOU Implementation Plans, (ii) management of program activities including integrated digital health systems rollout aligned with PNG's National Digital Health Strategy 2025-2030, (iii) coordination of U.S. Government implementing partners, provincial health authorities, and civil society organizations, and (iv) comprehensive reporting on outcome and process metrics. The Advisor will support the NDOH in carrying out life-saving humanitarian assistance (LHA) service delivery in full alignment with the new Presidential Executive Order (EO) directives. The Advisor will identify implementation bottlenecks and facilitate solutions through coordinated technical support.  The Health Expert will be based within the NDOH under the direction of appropriate Ministry staff serving as the onsite Manager/Supervisor and will report to the U.S. Department of State weekly and monthly. Familiarity with U.S. Department of State programming is highly desirable.

Responsibilities

Technical Leadership

The Advisor will provide strategic technical leadership to ensure effective implementation of the MOU between the US Embassy and the NDOH.

• Lead technical strategy and planning across the four Areas of Cooperation (Surveillance & Outbreak Response, Laboratory Systems, Data Systems, and Strategic Investment) while ensuring coherence across HIV, outbreak response, laboratory, and digital health systems
• Provide technical guidance on achieving MOU outcome metrics, including HIV cascade targets (diagnosis, treatment, viral suppression) and maternal and child health mortality reduction goals and in meeting the 7-1-7 detection and containment target.
• Advise on evidence-based approaches to strengthen PNG's health system resilience and infectious disease response capabilities, monitoring global best practices and recommending context-appropriate adaptations
• Ensure technical compliance with U.S. Government policies and PNG Government regulations, including technical input on the transition of U.S. Government-funded positions and systems to PNG Government management per MOU timelines

Management of Programs/Activity Implementation

The Advisor will oversee day-to-day management and coordination of MOU implementation activities to ensure timely achievement of process metrics and deliverables.

• Develop and monitor comprehensive work plans with clear timelines, milestones, and deliverables, tracking progress against MOU metrics and transition timelines for healthcare workers, laboratory staff, and data systems
• Coordinate implementation of surveillance and outbreak response activities, including field epidemiologist training, surge response mechanisms, and quality assurance across all program activities adhering to international standards
• Oversee rollout and integration of digital health systems (DHIS2, Open ELIS, VLSM, mSupply, Outbreak Information Management System)
• Identify implementation bottlenecks and manage risks, developing solutions and mitigation strategies in consultation with stakeholders while supporting capacity building for PNG Government staff assuming transitioned functions

Coordination of Partners, Technical Working Groups/Committees

The Advisor will serve as a primary liaison between the U.S. Government and PNG Government, facilitating effective coordination among all stakeholders.

• Serve as technical secretariat support to the GHS MSC and technical working groups, preparing materials, agendas, and documentation for quarterly MSC meetings and annual MOU review sessions in coordination with PNG's National Department of Health
• Coordinate with U.S. Government implementing partners (including FHI360 and other contractors) to ensure alignment with MOU objectives, and liaise with PNG Government ministries, departments, and provincial health authorities on implementation
• Facilitate coordination with the PNG eHealth Technical Working Group and Steering Committee on digital health system integration, and coordinate with multilateral organizations and development partners to maximize synergies and avoid duplication
• Build and maintain productive working relationships with key stakeholders at national and provincial levels, facilitating communication and information sharing between U.S. Government and PNG Government representatives

Communications:

• Regular conference calls with multisectoral stakeholders, US Embassy and GHSD Washington to review progress, discuss activities and address emerging issues.
• The GHS Technical Advisor should provide information and avail him/herself for calls/meetings with the US Embassy as requested.
• The Advisor will provide monthly reports to US Embassy/U.S. Department of State

Reporting:

The Advisor will establish and maintain comprehensive reporting systems to track MOU performance and ensure accountability.  He will provide a detailed monthly report to the U.S. Department of State submitted by the 5th day of the following month.  Additionally, the Advisor will submit a weekly progress report to U.S. Embassy/Department of State (and participate in weekly calls) to include a short paragraph about main successes for that week. 

• Develop and implement a monitoring and evaluation framework aligned with MOU metrics, tracking outcome and process indicators, infectious disease outbreak response timelines, and progress toward 2026-2030 targets
• Prepare comprehensive reports including quarterly progress reports for the MSC, annual performance assessments, and ad hoc reports as requested, ensuring compliance with U.S. Government accountability requirements to Congress
• Support audit and data management processes outlined in Section 4 (process metric, co-investment, and regulatory compliance audits), facilitate data collection under the Section 2.5.2 data sharing arrangement, and maintain comprehensive records of implementation activities
• Document lessons learned and alert Participants promptly to significant implementation challenges or risks to achieving MOU objectives, recommending modifications as appropriate during annual MOU reviews

Qualifications

• University degree in a relevant field and postgraduate degree in public health or epidemiology preferred.
• Minimum of seven years of program management experience in strategic planning, coordination, and evaluation of public health programs, with emphasis on disease, surveillance, prevention and outbreak response.
• Strong network and substantial experience working with ministerial level policy makers and multisectoral collaboration is an advantage.
• Demonstrated experience working in Papua New Guinea or the Pacific region.
• Familiarity with global health security programs

NoviSci, a division of Target RWE, is a data science organization with a dual mission:

1.  Developing best-in-class software to support the generation of RWE and
2.  Executing high-impact, tech-enabled scientific consulting and research.

Overview

We are currently seeking a Senior Epidemiologist to join a team of epidemiologists, statisticians, data engineers, and software developers. Together, you will lead the design and implementation of research studies using complex, real-world data. In this role, you will apply leading-edge methodology in epidemiology and statistics to solve important problems in health care.  

What You’ll Do

• Independently design and conduct research studies using advanced epidemiologic and statistical methods, such as causal inference and machine learning
• Lead a cross-functional technical team to ensure scientific integrity and methodological rigor across all phases of the study lifecycle including initial design, protocol development, implementation of statistical analysis, and dissemination of results
• Serve as a key scientific point of contact, engaging directly with clients and external collaborators. Comfort and proficiency in client-facing roles are essential skills 
• Disseminate study findings via study reports, presentations to internal and external stakeholders, peer-reviewed publications, and abstracts and presentations at professional conferences
• Provide technical support to the business development team to develop competitive scientific proposals 

What You’ll Bring

• Advanced degree (PhD or equivalent) in epidemiology, biostatistics, or a related quantitative discipline
• 4+ years of post-doctoral experience, preferably in a biotech or scientific consulting environment
• Experience with observational research methods for causal inference (e.g., inverse probability weighting, negative control outcomes/exposures, target trial emulation, quantitative bias analyses) coupled with a genuine intellectual curiosity to dig deep and explore novel approaches to answer hard questions
• Demonstrated experience leading research projects teams from conception to publication 
• Experience with administrative claims or electronic health record data, including familiarity with using diagnosis, procedure, and medication coding algorithms to operationalize eligibility criteria, exposure status, and clinical outcomes in real-world data.
• Strong aptitude for precise and impactful scientific writing evidenced by a record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation. 
• Strong organizational and planning skills including an ability to independently troubleshoot problems and think analytically in a fast-paced environment
• Willingness to take initiative while maintaining open lines of communication with colleagues and senior leadership. 
• Excellent time management skills and ability to multi-task and prioritize work

Nice-to-Have Background

• Expertise in statistical programming using R
• Experience mentoring junior research staff

If you’re excited to help support meaningful healthcare research, where your expertise directly contributes to rigor, trust, and improved patient outcomes, NoviSci is the place for you. We’re building something important, and we’d love for you to be a part of it.

What We Offer You

• Comprehensive health, dental, and vision coverage for you and your family
• 401(k) with company match
• Generous PTO and company holidays
• Paid parental leave
• Hybrid role: Located in Research Triangle Park, North Carolina

Epidemiologists

In the midst of an outbreak, our project teams rely on our epidemiologists to determine the spread and speed of a disease, as well as strategies for containment.

Responsibilities