Sr Project Manager, Digital Health Technology (DHT) & eCOA

FlagshipKansas; Topeka (KS); Hybrid; USD 229,233,000 - 272,214,000; Part time

Benefits offered by this job

Medical benefits

401k with company matching

Life insurance

Job summary

Eliassen Group seeks a Sr Project Manager, Digital Health Technology (DHT) & eCOA for a 12-month remote contract. The role bridges clinical operations, data management, clinical quality, and external technology partners, ensuring implementation quality and compliance of patient-facing digital tools.

Ideal candidate has 8+ years in biotech/pharma with eCOA experience, strong vendor and risk management, and a BA/BS in Life Sciences or related field; remote W2 with competitive benefits.

Qualifications

• 8+ years in biotechnology, pharma, or clinical trial tech.
• Deep mastery of eCOA systems development.
• Experience with ICH/GCP inspections and audits.
• Proven ability to lead cross-functional teams.
• Strong communication and data-driven decisions.

Responsibilities

• Serve as operational SME for digital health tech, including eCOA, wearables, and sensors.
• Own end-to-end study timelines and user requirements; execute UAT and license management.
• Plan and mitigate complex operational challenges from a clinical operations base.
• Coordinate cross-functional teams to align data flows with monitoring plans.
• Manage vendor performance and CAPAs; drive technical problem resolution.
• Develop and maintain SOPs/work instructions for DHT implementation.

Skills

eCOA systems

UAT

Vendor management

Clinical operations

Data management

Risk management

Education

BA/BS in Life Sciences

Tools

eCOA platforms

Job description

Job Description

Anywhere

Type: Contract

Category: Clinical Ops

Workplace Type: Remote

Standard Hours: Open

Reference ID: JN -092026-108484

Date Posted: 09/02/2026

Shortcut: http://careers.eliassen.com/oT7MpJ

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Description:

Remote

Our client seeks a Sr Project Manager, Digital Health Technology ( DHT ) & eCOA for a 12-month remote contract. The role serves as a bridge between clinical operations, data management, clinical quality, and external technology partners with accountability for implementation quality and compliance of patient-facing digital tools. The position combines a clinical operations background with specialized expertise in eCOA systems and wearable device development processes, managing the technical trial lifecycle from study design through close-out with an agile and innovative mindset.

Due to client requirements, applicants must be willing and able to work on a w2 basis. For our w2 consultants, we offer a great benefits package that includes Medical, Dental, and Vision benefits, 401k with company matching, and life insurance.

Rate: $80.00 to $95.00/hr. w2

JN -092026-108484

Responsibilities:

• Serve as the primary operational SME and escalation point for assigned digital health technologies, including eCOA (ePRO, ClinRO, ObsRO), eConsent, wearables, and sensors.
• Provide technical and operational input into protocol development related to digital tools and technologies.
• Own end-to-end technical project timelines, author, review, and approve study specifications and user requirements, execute UAT , and manage acquisition of COA instrument licenses.
• Plan, execute, and monitor proactive mitigation plans for complex operational challenges using a clinical operations foundation.
• Liaise with cross-functional teams to ensure cohesive trial execution, align technical data flows with the Medical Monitoring Plan, and oversee monitoring as it pertains to digital tools, data compliance, and site performance.
• Directly manage specialized vendor performance, conduct root cause analyses for system variances, implement CAPAs, and provide technical problem resolution.
• Monitor and manage study-level DHT financial components including contracts, change controls, adjustments, KPIs/KQIs/KRIs, and pass-through costs.
• Provide operational guidance, training, and technical mentorship to junior Clinical Operations staff.
• Partner with Clinical Quality to align DHT processes with internal quality systems, inspection readiness, and evolving regulatory guidance ( ICH - GCP , eCOA-related expectations).
• Lead or contribute to risk assessments for digital technologies and incorporate findings into study-level and program-level risk management plans.
• Develop, review, and maintain SOPs, work instructions, and process guidance for DHT and eCOA implementation, validation, and oversight.

Experience Requirements:

• Minimum of approximately 8+ years within biotechnology, pharmaceuticals, or clinical trial technology platforms.
• Proven track record managing trials with a multi-dimensional Clinical Operations background and deep mastery of eCOA systems development.
• Direct experience participating in or leading ICH / GCP inspections, internal quality audits, and inspection preparedness initiatives.
• Demonstrated understanding of clinical trial conduct, GCP , and study operations.
• Strong communication, relationship-building, and presentation skills.
• Ability to lead and collaborate with cross-functional teams to drive operational excellence.
• Data-driven approach to planning, execution, risk mitigation, and technical problem-solving.
• Solutions-oriented with the ability to challenge status-quo thinking to drive high-efficiency solutions.
• Agility to adapt to shifting trial environments with an innovative mindset.

Education Requirements:

• Minimum BA/BS in Life Sciences, Computer Science, Public Health, Information Systems, or related field.

Eliassen is committed to building a diverse and inclusive team from a variety of backgrounds, perspectives, and skills. We are an Equal Opportunity and Affirmative Action Employer and all employment decisions are based on merit, performance, and business needs. Eliassen does not discriminate on the basis of race, color, gender identity or expression, sexual preference or orientation, sex (including pregnancy, childbirth, and related medical conditions), marital status, creed, religion, physical or mental disability, genetic information, military or veteran status, age, ancestry, national origin, citizenship status, prohibited criminal record inquiries of applicants and employees, or any other category protected by federal, state, or local laws.

About Eliassen Group:

Eliassen Group is a strategic consulting firm that helps organizations reach further and achieve more through our technology, business advisory, and life sciences solutions. For nearly 40 years, we have combined exceptional people, deep domain expertise, and intelligent capabilities to expand our clients’ capacity and accelerate meaningful outcomes. We are driven by a purpose to positively impact the lives of our employees, clients, consultants, and the communities we serve.