Clinical Research Change Management Consultant

Vitalief
New Brunswick, NJ
About Vitalief
Vitalief is a consulting firm dedicated to helping Sites, Sponsors, and CROs optimize research operations, reduce costs, and accelerate innovations that improve patient care. By combining deep clinical research expertise with practical, results-oriented consulting, we help organizations enhance operational efficiency and achieve sustainable growth.

The Role
We are seeking a highly experienced Clinical Research Change Management Consultant to lead clinical trial operational assessments for our clients, including large Academic Medical Centers and multi-location community hospital systems. This role will serve as the primary subject matter expert (SME) for comprehensive current-state operational assessments across Technology, Organization, Process, People, and Finance, supporting both Oncology and Non-Oncology clinical research programs.

The ideal candidate brings deep expertise in organizational transformation and change management within complex healthcare and research environments, with a proven ability to drive stakeholder alignment, operational adoption, and sustainable process improvement across multi-site systems.

You will collaborate closely with the Vitalief delivery team to conduct structured stakeholder interviews, assess operational effectiveness, identify organizational and workflow gaps, and deliver actionable recommendations along with a scalable transformation roadmap to hospital leadership.

Engagement Details
  • Work Hours: from 20 to 40 hours/week
  • Contract Duration: from 1 to 3 months ( possible extension and/or conversion to a Vitalief full time employee ).
  • Pay Rate: Market competitive (depends on experience level).
  • Location: Remote (EST zone work hours) with up to 10% travel domestically.
Responsibilities
  • Serve as the lead Clinical Research SME for the engagement, guiding all aspects of the operational assessment and change management strategy.
  • Conduct in-depth interviews with clinical research staff and stakeholders across the clinical trial lifecycle to identify operational gaps, bottlenecks, communication challenges, and improvement opportunities across Oncology and Non-Oncology programs.
  • Partner with executive and operational stakeholders to assess organizational readiness for change and recommend sustainable transformation strategies.
  • Collaborate with the Vitalief team to design effective interview templates, assessment methodologies, and change management frameworks.
  • Evaluate current-state workflows, governance structures, staffing models, and technology utilization to identify opportunities for operational alignment and standardization.
  • Compare Oncology and Non-Oncology operations to identify transferable best practices and opportunities for cross-functional integration.
  • Develop prioritized, actionable recommendations that address immediate operational challenges while supporting long-term scalability and organizational adoption.
  • Create and present a clear transformation roadmap focused on operational excellence, stakeholder engagement, process optimization, and effective cross-system coordination.
  • Provide regular project status updates to executive stakeholders, ensuring alignment, transparency, and on-time delivery of engagement milestones.
  • Deliver executive-level presentations summarizing findings, recommendations, change impacts, and measurable next steps.
Qualifications
  • 15+ years of progressive clinical research operations experience, preferably within Academic Medical Centers and/or community hospital systems.
  • Bachelor’s degree in life sciences, healthcare, or related field (or equivalent combination of education and experience).
  • Proven experience leading operational assessments, organizational transformation, and enterprise-level change management initiatives.
  • Experience supporting Oncology and Non-Oncology clinical trial operations preferred.
  • Strong knowledge of change management methodologies, stakeholder engagement, and organizational adoption strategies.
  • Prior consulting experience delivering strategic solutions to healthcare or research clients is preferred.
  • Executive-level communication, facilitation, and presentation skills with the ability to clearly convey complex findings.
  • Demonstrated success influencing stakeholders and driving operational improvements in complex, matrixed environments.
  • Expertise with research operations technologies, including CTMS, EMR integrations, workflow tools, and analytics platforms.
  • Strong analytical, financial, and problem-solving skills, including risk assessment and mitigation planning.
  • Proven ability to build C-suite relationships, lead cross-functional initiatives, and mentor high-performing teams.
  • Strategic, collaborative, and results-oriented leader who thrives in fast-paced environments.
Preferred Skills
  • Experience leading large-scale organizational change, transformation programs, or post-merger operational integration initiatives.
  • Experience managing consulting delivery teams, including role definition, coaching/mentoring, and performance management.
  • Strong general management and P&L oversight experience.
  • Familiarity with change management frameworks such as Prosci, ADKAR, Lean, or similar methodologies.
Physical Demands
Prolonged periods of sitting at a desk and working at a computer. Standing, walking, visual perception, talking, and hearing. Ability to lift up to 20 lbs. Limited travel to various physical locations domestically.

Posted 2026-05-09

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