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Associate Director, Epidemiology

About N-Power Medicine

N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients. We are building an exceptional multi-disciplinary team with diverse expertise spanning healthcare, engineering, technology and regulatory, and with people who share our core value of Empowering Community through generosity, curiosity and humility.  We are working with urgency to bring better therapies to patients faster. 


Position Overview

N-Power Medicine integrates demographic, clinical and molecular data across a network of large health systems. N-Power Medicine’s vision is to combine prospective and retrospective data  originating from both prospective and retrospective sources, including human-based abstraction as well as direct EMR ingestion, to enable the next generation of external controls, for faster and more efficient clinical trials. The epidemiology group at N-Power Medicine is an important contributor to these efforts across data capture, data standardization and normalization, data analysis, product development, and clinical trial study support. Epidemiology plays a critical role in supporting our health system and life science partners, as well as our product portfolio.


As the Associate Director of Epidemiology, you’ll interact with a diverse team to drive the development of external control arms, data insights in our products, research studies, and publications.

This position is remote within the United States.


Role Objectives and Responsibilities

-Design, implement, interpret, report and publish the results of retrospective and prospective observational research studies that demonstrates the utility of real-world data (RWD) for life sciences and health system customers

-Support the development of N-Power Medicine’s data platform and assets, including specification of data models and clinical nomenclature/coding requirements to efficiently harmonize real-world data with clinical trials data standards, such as Clinical Data -Interchange Standards Consortium (CDISC)

-Contribute to developing N-Power Medicine’s real-world evidence generation platform, in alignment with the company’s by-protocol, prospective real-time registry data 

-Collaborate with internal partners (Clinical Science, Commercial, and Network Partners) to develop the company's strategic partnerships with life sciences and health systems

-Collaborate with internal partners (Clinical Science, Commercial, and Network Partners) to  develop the data requirements to support N-Power Medicine’s next-generation External Controls methodology and product offerings

-Help translate the perspectives and requirements of FDA and regulatory agencies around external controls to inform N-Power Medicine's data capture/collection and platform requirements

-Ask the right scientific questions, ideate and make recommendations on fit-for-purpose data and analytics solutions 

-Stay current with novel data analysis methods for observational data, in particular Causal Inference and its applications to clinical trials


Education, Experience, Behavioral Competencies, & Skills

-12+ years of experience with a Bachelor’s Degree, 8+ years of experience with a Master’s Degree and 5+ with a PhD in epidemiology

-Graduate degree in Epidemiology, Biostatistics or Related field, PhD with an emphasis in epidemiology preferred

-Knowledge of RWD study design and execution

-Experience with data analysis, specifically from observational study designs 

-Experience with epidemiological, registry, EMR, and/or claims data

-Experience using R, Python, SQL or similar and a highly technical acumen

-Experience summarizing data and disseminating insights to multi-disciplinary audiences

-Experience with managing budget, timelines, and relationships with key stakeholders, including Lifescience partners and other strategic collaborators.

-Confident in presenting the NPower brand in scientific conferences and other professional forums.

-Understanding of drug development, regulatory requirements and processes

-You are a doer, self motivated, and driven

-Comfortable within a growth stage environment

-Effective scientific communication; written and verbal

-Cancer expertise, strong publication history, and teaching/mentoring experience is preferred

-Generous, Curious, and Humble


Travel Requirements 

Up to 15% of time required to travel in role (out of 100%)


Pay Information

The expected salary range for this position is $165,000 and $248,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. N-Power Medicine (NPM) offers equity at hire as well as a discretionary annual bonus which may be available based on Company performance. This position is eligible for company benefits. 


More About Us:

We are a mission-driven, well-funded, rapidly growing company, eager to attract passionate professionals offering a highly attractive compensation package with a balanced and flexible work environment, competitive industry benefits as well as a 401K plan and other great company “perks.”


We are an Equal Opportunity Employer and value diversity at our company. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.


Covid-19 Policy –  The Company is committed to providing and maintaining a safe workplace, and to safeguard the health and well-being of our employees, families, visitors, and the community. While vaccination remains one of the most important tools in advancing the health and safety of employees and promoting the efficiency of workplaces, we are now in a different phase of our response when these measures are no longer necessary. We currently do not have mandatory COVID-19 vaccination requirements for our employees and contractors, as the COVID-19 public health emergency has ended. However, there are certain N-Power Medicine employees and contractors who, based on their role, will be required to continue to follow our 2021 COVID-19 vaccination and other requirements as mandated by N-Power Medicine’s partners they serve. We reserve the right to modify or amend our corporate policy at any time.


Applicants must be currently authorized to work in the U.S. on a full-time basis. The Company will not sponsor applicants for work visas.



Average salary estimate

$206500 / YEARLY (est.)
min
max
$165000K
$248000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Associate Director, Epidemiology, N-Power Medicine

At N-Power Medicine, we're on a mission to revolutionize drug development and reshape clinical trials by integrating healthcare practice with cutting-edge research. We are excited to invite an Associate Director, Epidemiology extraordinaire to join our dynamic remote team! This role is pivotal as you will be immersed in designing, implementing, and interpreting both retrospective and prospective observational research studies that draw on real-world data, making tangible contributions to our life science partners and health systems. Your work will not only drive our data insights but also help convey complex scientific concepts at conferences, ensuring our positions resonate with the medical community. Here, collaboration is key, and as you team up with specialists across Clinical Science, Commercial, and Network Partners, your contributions will help refine methodologies for next-gen External Controls, enhancing our unique data platform. With more than a dozen years of experience under your belt and a strong educational foundation—ideally, a PhD in epidemiology—you'll leverage your knowledge to engage effectively with stakeholders, drive evidence generation, and satisfy regulatory needs. At N-Power Medicine, we cherish curiosity, humility, and a collaborative spirit, striving to empower communities while delivering improved therapies to patients faster. If you have a knack for scientific communication and a desire to team up in a growing environment, this associate director role could be your next big step in forging impactful innovations.

Frequently Asked Questions (FAQs) for Associate Director, Epidemiology Role at N-Power Medicine
What are the primary responsibilities of the Associate Director, Epidemiology at N-Power Medicine?

The primary responsibilities of the Associate Director, Epidemiology at N-Power Medicine include designing, implementing, and reporting observational research studies that utilize real-world data. This role also entails collaborating with multi-disciplinary teams to advance the company's data platforms, develop external control methodologies, and support strategic partnerships with life sciences and health systems.

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What qualifications are required for the Associate Director, Epidemiology position at N-Power Medicine?

To qualify for the Associate Director, Epidemiology position at N-Power Medicine, candidates should have at least 12 years of experience with a Bachelor’s Degree, 8 years with a Master’s Degree, or 5 years with a PhD in epidemiology. Additionally, experience in study design, data analysis, and familiarity with regulatory requirements is essential.

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How does the Associate Director, Epidemiology contribute to clinical trial innovations at N-Power Medicine?

The Associate Director, Epidemiology contributes to clinical trial innovations at N-Power Medicine by leveraging real-world data to establish external control arms and enhance evidence generation strategies. Their insights help inform data collection requirements, aligning methodologies with regulatory standards to foster efficient and effective trial designs.

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What skills are essential for success in the Associate Director, Epidemiology role at N-Power Medicine?

Essential skills for success in the Associate Director, Epidemiology role include advanced statistical knowledge, experience with observational studies, proficiency in data analysis tools like R or SQL, and effective scientific communication. Additionally, strong project management capabilities and the ability to collaborate with various stakeholders are critical.

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What is the work environment like for an Associate Director, Epidemiology at N-Power Medicine?

The work environment for an Associate Director, Epidemiology at N-Power Medicine is remote, promoting a flexible work-life balance. Team members are engaged in a growth-oriented culture where diversity and collaboration are valued, allowing for dynamic contributions to meaningful healthcare innovations.

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Common Interview Questions for Associate Director, Epidemiology
How do you approach designing observational research studies?

When designing observational research studies, I start with clear objectives and hypotheses. I then ensure to identify appropriate data sources, and incorporate robust methodologies that align with regulatory standards while focusing on data quality. By collaborating with stakeholders for input and feedback throughout the process, I ensure that the research aligns with real-world applications.

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Can you describe your experience with real-world data (RWD)?

I have extensive experience working with real-world data, leveraging it to inform research questions and validate clinical outcomes. My background includes integrating various data types, ensuring adherence to regulatory requirements, and using RWD insights to enhance clinical trials and health outcomes for clients.

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What strategies do you employ for effective communication with multi-disciplinary teams?

I prioritize open, transparent communication by utilizing clear and concise language. I adapt my communication style to suit diverse audiences and foster an environment where questions are encouraged. Regular meetings and updates, along with collaborative tools, help maintain alignment and progress across departments.

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Describe a successful project where you implemented new methodologies in epidemiology.

In a recent project, I spearheaded the development of a new methodology for analyzing longitudinal RWD by integrating causal inference techniques. This resulted in improved insights into treatment outcomes, garnering positive feedback from stakeholders. We were able to provide robust evidence that supported a client's drug approval process.

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How do you stay updated with novel data analysis methods?

To stay updated with novel data analysis methods, I regularly attend workshops, webinars, and conferences focused on epidemiology and data analysis. I also engage with academic literature, participate in professional networks, and collaborate with colleagues to share insights on emerging trends and techniques.

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What is your experience with regulatory standards in epidemiology?

My experience with regulatory standards includes navigating the requirements set by the FDA for clinical trial data. I've worked closely with regulatory bodies to ensure that our observational studies comply with necessary protocols, ultimately facilitating smoother approvals and enhanced study credibility.

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How do you handle tight deadlines when managing projects?

When faced with tight deadlines, I prioritize my tasks, breaking projects into manageable components and delegating tasks to team members where necessary. I maintain open communication with stakeholders to manage expectations and ensure deliverables are met without compromising quality.

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Can you explain the importance of collaboration in epidemiological research?

Collaboration in epidemiological research is critical as it brings together diverse expertise and perspectives, enhancing the quality of research designs and outcomes. It fosters creativity, innovation, and ensures that multiple viewpoints are considered, aligning with varied stakeholder needs and real-world challenges.

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How do you ensure data integrity and quality in your studies?

I ensure data integrity and quality by implementing rigorous data management protocols, including validation checks, cross-verification with original sources, and ongoing training for team members on best practices. Regular audits and compliance checks also play a vital role in maintaining high standards throughout the study.

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What inspires you to work in the field of epidemiology?

My inspiration to work in epidemiology stems from my passion for public health and the desire to impact patient outcomes positively. The ability to derive meaningful insights from data that drive better healthcare decisions motivates me to continuously seek advancements in research methodologies and data analysis.

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n-power medicine, a venture-backed startup, aims to transform clinical trials by reinventing the ‘how’. we are empowering community oncology sites to become high-performing clinical trial centers by providing resources and staff to increase the ...

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