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Clinical Research Strategic Management Consultant

Part-time

Vitalief

Remote · USPart-timePosted 7mo agoSeen in employer's feed 3 days ago

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At a glance

Compensation
No compensation found
Location
Remote · US
Schedule
Part-time
Work Authorization
US work authorization required

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Vitalief is hiring a Clinical Research Strategic Management Consultant. Vitalief is seeking a highly experienced Clinical Research Strategic Management Consultant to lead a short-term engagement for a multi-location community hospital system. This role will serve as the primary subject matter expert for a comprehensive current-state operational assessment across Technology, Organization, Process, People, and Finances, with a strong focus on Non-Oncology programs and cross-system communication effectiveness. The consultant will collaborate with the Vitalief delivery team to conduct stakeholder interviews, analyze findings, and deliver actionable recommendations and a transformation roadmap...

Key focus areas include Serve as the lead Clinical Research SME for the engagement, guiding all aspects of the operational assessment., Conduct in-depth interviews with clinical research staff and stakeholders across the trial lifecycle to identify gaps, bottlenecks, and improvement opportunities for Non-Oncology operations., and Collaborate with the Vitalief team to design effective interview templates and assessment tools..

Successful candidates bring 15+ Years Clinical Research Operations, Bachelor's In Life Sciences/Healthcare, and Operational Assessments Experience. Important skills include Clinical Research SME, Operational Assessment, Process Improvement, Organizational Transformation, Consulting, and Executive Presence. Preferred (not required): Oncology Operations Experience, Role Definition, Coaching/Mentoring, and Performance Management.

Skills & qualifications

RequiredNice to have

Skills

Clinical Research SMEOperational AssessmentProcess ImprovementOrganizational TransformationConsultingExecutive PresenceNegotiation SkillsPresent Complex FindingsInfluence StakeholdersInnovative SolutionsCTMSEMR IntegrationAnalytics ToolsAnalytical SkillsQuantify Financial BenefitsQuantify Operational BenefitsAssess RiskDesign Mitigation StrategiesBuilding C-Suite RelationshipsLeading Large-Scale Change InitiativesStrategic ThinkingResults-OrientedCollaborative Leadership StyleBuilding High-Performing Cross-Functional TeamsOncology Operations ExperienceRole DefinitionCoaching/MentoringPerformance ManagementGeneral ManagementP&L Oversight Experience

Qualifications

15+ Years Progressive Clinical Research Operations ExperienceBachelor's Degree in Life Sciences, Healthcare, or Related Discipline or Equivalent Combination of Education and Experience

Full job description

About Vitalief

Vitalief partners with Sites, Sponsors, and CROs to streamline research operations, reduce costs, and accelerate breakthroughs that improve patient care. We bring deep clinical research expertise together with practical, results-driven consulting to help organizations operate more efficiently and achieve sustainable growth.

The Role

We are seeking a highly experienced Clinical Research Strategic Management Consultant to lead a short-term engagement for a multi-location community hospital system. This role will serve as the primary subject matter expert (SME) for a comprehensive current-state operational assessment across Technology, Organization, Process, People, and Finances, with a strong focus on Non-Oncology programs and cross-system communication effectiveness.

You will collaborate closely with the Vitalief delivery team to conduct structured stakeholder interviews, analyze findings, and deliver actionable recommendations and a transformation roadmap to hospital leadership.

Engagement Details

  • Part-Time: up to 20 hours/week

  • Contract Duration: 2 months (possible extension)

  • Pay Rate: Market competitive (depends on experience level)

  • Location: Remote (EST zone work hours) with 1 early-stage on-site visit (expenses covered). Travel location is Northeastern USA.

If you’re a strategic thinker who thrives on solving complex operational challenges in clinical research, we’d love to hear from you.

Responsibilities

  • Serve as the lead Clinical Research SME for the engagement, guiding all aspects of the operational assessment.

  • Conduct in-depth interviews with clinical research staff and stakeholders across the trial lifecycle to identify gaps, bottlenecks, and improvement opportunities for Non-Oncology operations.

  • Collaborate with the Vitalief team to design effective interview templates and assessment tools.

  • Compare Oncology and Non-Oncology operations to surface transferable best practices.

  • Develop prioritized, actionable recommendations to address immediate operational deficiencies while protecting long-term integration potential.

  • Outline a clear transformation roadmap to achieve operational excellence and improved coordination across the system.

  • Provide regular project status updates to executive stakeholders, ensuring alignment and on-time delivery of all engagement milestones.

  • Deliver a final executive-level presentation summarizing findings, recommendations, and measurable next steps.

Qualifications:

  • 15+ years progressive clinical research operations experience, ideally within community hospital settings.

  • Bachelor’s degree in life sciences, healthcare, or related discipline (or equivalent combination of education and experience).

  • Proven experience in operational assessments, process improvement, and organizational transformation.

  • Prior consulting experience delivering value-added services to external clients.

  • Strong executive presence, negotiation skills, and the ability to present complex findings with clarity and confidence.

  • Demonstrated ability to influence stakeholders to adopt innovative, “outside-the-box” solutions.

  • Expertise in research operations technologies (CTMS, EMR integration, analytics tools).

  • Strong analytical skills with the ability to quantify financial/operational benefits, assess risk, and design mitigation strategies.

  • Demonstrated success in building C-suite relationships and leading large-scale change initiatives in complex, multi-stakeholder environments.

  • Strategic thinker who thrives in fast-paced, entrepreneurial environments.

  • Highly driven, results-oriented, and competitive with a collaborative leadership style.

  • Skilled at building high-performing, cross-functional teams.

Preferred Skills:

  • Oncology and Non-Oncology operations experience.

  • Experience managing consulting delivery teams, including role definition, coaching/mentoring, and performance management.

  • Strong general management and P&L oversight experience.

PHYSICAL DEMANDS: Prolonged periods of sitting at a desk and working at a computer. Standing, walking, visual perception, talking and hearing. Lifting up to 20lbs. Limited travel to various physical locations domestically in Northeastern USA.

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