Connected Devices - Solution Implementation Lead

IQVIA Inc

Cataluña

Remote

EUR 90,000 - 120,000

Full time

5 days ago
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Job summary

IQVIA is seeking a Solution Implementation Lead to own end-to-end startup execution of new connected medical device and digital health solutions. The role focuses on respiratory service line initiatives and ensures readiness from concept to Business Go-Live.

The ideal candidate has 10+ years in healthcare/digital health, strong PM skills, and expertise across regulatory, validation, and cross-functional delivery within a regulated environment. Remote in Europe/EMEA.

Qualifications

  • 10+ years of relevant healthcare/digital health experience.
  • Bachelor’s degree or equivalent in a related field.

Responsibilities

  • Own end-to-end startup execution from business case approval through Business Go-Live.
  • Develop and manage startup plan with milestones, dependencies, risks and mitigations.
  • Coordinate across Engineering, IT, Validation, QA, Regulatory, Data Management, Operations, Logistics, Vendors, Field Support and Training.
  • Translate solution concepts into clear device, system, service and validation requirements for technical teams.
  • Lead governance and stakeholder communications on startup status, risks and readiness.

Skills

Digital health
Regulated clinical environments
PM/Program management
Stakeholder management
Executive-level presentations
Technical aptitude
Leadership

Education

Bachelor’s degree or equivalent

Job description

The Solution Implementation Lead is the end‑to‑end execution owner and subject‑matter expert for the development, validation, and operationalization of new connected medical device and digital health solutions.

This role partners closely with the Strategic Solutions Lead to evaluate, shape, and deliver new solution offerings aligned to the strategic priorities of the Connected Devices business, with a primary focus on the respiratory service line. The role bridges strategy, execution, validation, and operational readiness, ensuring solutions progress from concept through Business Go‑Live and are ready for scalable study deployment.

Key Responsibilities and Oversight

Experience supporting respiratory clinical trials (e.g., asthma, COPD, pulmonary indications) is required. Candidates without direct respiratory trial experience clearly demonstrated within their resume will not be considered.

Solution Evaluation & Strategy Support
  • Partner with Strategic Solutions Leads (SSL) to evaluate new digital health and medical device solutions aligned to Connected Devices strategy.
  • Provide SME input into solution feasibility, operational workflows, regulatory considerations, and validation approach.
  • Support Strategic Solutions as needed with business case development, budget inputs, go-to-market strategy and customer‑facing SME in customer presentations.
End‑to‑End Solution Startup Execution Ownership
  • Own end‑to‑end execution of approved solutions from business case approval through Business Go‑Live, serving as the single point of accountability for startup outcomes.
  • Develop and manage the startup plan, including milestones, dependencies, risks, constraints, and mitigation strategies.
  • Ensure solution design, operational workflows, and validation activities are aligned with study, program, and stakeholder needs.
  • Confirm readiness at each startup stage and before Business Go‑Live.
Cross‑Functional Orchestration & Technical Leadership
  • Lead and coordinate execution across Engineering, IT, Validation, QA, Regulatory, Data Management, Operations, Logistics, Vendors, Field Support and Training.
  • Translate high‑level solution concepts into clear device, system, service, and validation requirements understood by technical and validation teams.
  • Support vendor relationships, including issue resolution, design alignment, and budget collaboration.
  • Provide expert troubleshooting guidance to operations and support teams; engage with sites and customers as needed to resolve complex issues.
Solution‑Level Readiness, Quality & Compliance
  • Ensure solution‑level readiness, including documentation, validation completion, training delivery, support models, and escalation pathways.
  • Partner closely with Solution Specialists to ensure regulatory and compliance requirements are met without late‑stage disruption.
  • Lead quality management, process improvement, and continuous improvement initiatives.
  • Contribute to internal SOPs, study templates, and site/patient‑facing materials as a solution SME.
Governance, Escalation & Stakeholder Management Oversight
  • Own resolution of startup‑level issues; elevate appropriately when:
  • Scope or solution intent is impacted (to Strategic Solutions Lead)
  • Timeline, investment, or delivery risk requires acceptance (to Governance / Sponsor)
  • Provide clear, consistent communications to internal stakeholders, sponsors, and leadership on startup status, risks, and readiness.
  • Transfer ownership at Business Go‑Live to study execution leadership (e.g., CD Project Manager) and retain an escalation/support role for solution‑level issues post‑handoff.
Required Knowledge, Skills & Abilities
  • Strong knowledge of digital health, connected medical devices, and regulated clinical environments is required and must be clearly outlined in your resume/CV.
  • Working knowledge of FDA guidelines and global regulatory expectations and their operational impact.
  • Advanced project and program management skills in complex, matrixed organizations.
  • Excellent technical aptitude related to systems, platforms, integrations, and device workflows.
  • Strong communication, stakeholder management, and executive‑level presentation skills.
  • Proven ability to establish and maintain effective working relationships with internal teams, vendors, sponsors, sites, and clients.
  • Occasional travel may be required.
Minimum Education & Experience
  • Bachelor’s degree or equivalent combination of education, training, and experience.
  • 10+ years of relevant experience in healthcare, pharmaceutical, life sciences, or digital health environments.
  • Demonstrated leadership experience managing people, operations, and cross‑functional initiatives.
  • Strong business acumen with experience supporting solution development, commercialization, and delivery.

This is a remote opportunity open to candidates currently residing in EMEA.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi‑talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

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