Clinical Research Strategic Management Consultant
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 14h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
First seen 14d ago
No source stated a posting date, so this is when the listing first reached us — which is a floor, not the real age. Last seen at its source just now.
We have tracked this listing since 18 Oct 2026 (14 days). The employer's own board has carried it every time we have read it, most recently just now.
Is it remote?
Remote
That is the location the employer filed this posting under. Quoted as written — we do not re-word the source's own location.
Who may apply?
Not stated
The description states no restriction of its own. This is the source's own tag.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
JazzHR employer's own board first seen 14d ago · last seen just now
The listing
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.
#LI-DNP