Digital Patient Scientist - Evinova

Evinova is a health-tech business focused on accelerating better health outcomes by advancing digital transformation across the life sciences sector. By combining science-based expertise, evidence-led rigor, and deep human insight, we design digital solutions that enable healthcare to work better for everyone. Operating at the intersection of healthcare, technology, data, and analytics, we are helping unlock the full potential of digital health, transforming how clinical research is conducted, how care is delivered, and how patients experience healthcare. Our solutions are built to scale, driving efficiency, improving decision-making, and ultimately delivering better outcomes for patients worldwide.

At Evinova, we are driven by a shared purpose to transform health through data and digital innovation. Our teams collaborate across disciplines to solve complex challenges, continuously learning and evolving in a fast-paced, high-impact environment. We also recognize the importance of flexibility and balance. Our ways of working support both individual needs and team collaboration. To foster connection and collaboration, employees are expected to work from the office three days per week, creating opportunities for in-person teamwork, innovation, and meaningful connection.

About The Team

We're building out a best-in-class Digital Science team to leverage innovative digital technology, apply user-centric design, and use science to improve participation in clinical research, collect novel and/or better data, apply advanced analytics to inform more robust evidence, and support both patients and their healthcare providers towards better care and improved outcomes.

About The Role

As a Senior Scientist, you’ll turn unmet patient and clinical needs into innovative digital solutions that help patients, care partners, and healthcare professionals capture, understand, and act on health information throughout a clinical trial. You’ll work at the forefront of digital health innovation, developing remote patient monitoring (RPM) solutions and other digital tools spanning symptom and toxicity monitoring, wearables and sensors, medication tracking, and intelligent alerting and escalation. You’ll help take solutions from early concept and scientific design through validation and real-world implementation in clinical studies. Working alongside experts across Digital Science, Product, Design, Data Science, and clinical study teams, you’ll have the opportunity to influence how digital technologies are used across therapeutic areas including oncology, cardiovascular, renal and metabolism, and respiratory and immunology, ultimately helping make clinical trials more connected, patient-centric, and effective.

Responsibilities

• Opportunity Scoping and Concept Definition
  • Identify and prioritize opportunities for new digital solutions, including remote patient monitoring (RPM), dosing diaries, wearables, and other patient- and HCP-facing tools.
  • Define the intended use, target population, decision context, and value proposition for new solutions.
  • Evaluate existing instruments, devices, and sensors before recommending new development.
• Instrument, Algorithm, and Functionality Development
  • Lead the scientific design of digital measures and functionality, including assessments, scoring algorithms, thresholds, alerts, and escalation pathways.
  • Translate scientific requirements into clear specifications for Product, Design, and Engineering.
  • Review and test solutions throughout development to ensure they deliver on their scientific intent.
• Clinical Validity and User-Centred Design
  • Bring the needs and behaviors of patients, caregivers, and HCPs into the design of digital solutions.
  • Partner with Design to create intuitive, accessible experiences for diverse populations, including older, unwell, and digitally less confident users.
  • Ensure solutions support reliable data collection while minimizing participant burden.
• Evidence Generation and Data Collection Methodology
  • Design qualitative and quantitative research to establish content validity, usability, and fitness for purpose.
  • Develop data collection approaches that respect participant privacy and generate meaningful, actionable insights.
  • Ensure analytical and reporting approaches align with relevant regulatory expectations.
• In-Trial Implementation and Deployment
  • Support the implementation and deployment of digital solutions within clinical trials, including clinical documentation and training materials.
  • Provide ongoing scientific oversight and help resolve data collection, algorithm, and usability challenges.
  • Serve as a Digital Science partner to clinical study teams throughout trial delivery.
• Engagement, Adherence, and Behavioral Insight
  • Develop strategies to improve patient, caregiver, and HCP engagement, including reminders, personalized feedback, and notification design.
  • Apply behavioral science principles to encourage consistent reporting and adherence to treatment and study procedures.
  • Develop content that helps participants confidently use digital tools, medications, and self-administered devices.
• Evaluation, Iteration, and Documentation
  • Partner with Data Science and Analytics to define KPIs and evaluate engagement, compliance, data quality, and clinical utility.
  • Use insights from live solutions to continuously improve digital features and experiences.
  • Develop scientific and regulatory documentation and represent the scientific rationale for solutions with study teams, governance groups, sponsors, and health authorities.

Requirements

Education

A combination of academic training and practical experience in outcomes research, including one of the following:

• Doctoral degree (Ph.D., Sc.D., Dr.P.H. or equivalent) in a relevant discipline such as health services research, health outcomes research, epidemiology, pharmacy administration, public health, economics, statistics, or decision sciences.
• Clinical degree in medicine, pharmacy, or nursing plus a master’s degree in a related discipline.
• Master’s degree in a relevant discipline plus at least two years of practical experience.
• Bachelor’s degree in a relevant discipline plus at least five years of practical experience.

Technical Expertise

• Working knowledge of clinical drug development.
• Experience translating clinical or patient needs into the design of a data collection tool, instrument, algorithm, or digital feature.
• Strong project management skills with the ability to lead multiple development workstreams in parallel.
• Strong conceptual, analytical, and critical-thinking skills.
• Ability to navigate ambiguity, solve complex problems, and adapt quickly in a fast-paced environment.
• Creative, innovative, and solution-focused approach, with a willingness to challenge the status quo and take ownership.
• Strong communication and relationship-building skills across scientific, technical, and commercial stakeholders.

Qualifications

The following experience is desirable for the role:

• Experience developing digital applications for healthcare, wellness, or clinical research.
• Experience with remote patient monitoring, ePRO/eCOA, or other digital health technologies used in clinical trials.
• Knowledge of clinical outcome assessment (COA) methodologies, including content validity, cognitive debriefing, and psychometric evaluation.
• Familiarity with toxicity grading frameworks such as CTCAE and PRO-CTCAE.
• Experience working with data from multiple sources, including wearables and sensors.
• Therapeutic area expertise in oncology and/or knowledge of treatment-related toxicity management.
• Understanding of digital development frameworks and the regulatory landscape for digital health technologies and clinical outcome assessments.
• Experience conducting outcomes research and communicating findings to internal and external audiences.
• Strong attention to detail with the ability to manage multiple concurrent activities.
• Resilience and adaptability, with the ability to motivate others through change.

Pay

The annual base pay for this position ranges from $115,899.20 - $152,117.70 USD. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, this position offers a short-term incentive bonus opportunity and eligibility to participate in our equity-based long-term incentive program.

Benefits

• Qualified retirement program (401(k) plan).
• Paid vacation and holidays.
• Paid leaves.
• Health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans.

Date Posted: 23-Aug-2026