Project Manager 2, SCCC

University of MiamiMiami, FL
Onsite

About The Position

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Project Manager 2 to work at the UHealth campus in Miami, Fl. The Project Manager 2, SCCC (H), manages multiple SCCC projects of moderate complexity across departments. Leads cross-functional teams, coordinates resources, and ensures successful execution aligned with strategic priorities.

Requirements

  • Bachelor’s degree in a relevant field
  • Minimum 3 years of relevant experience
  • Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
  • Teamwork: Ability to work collaboratively with others and contribute to a team environment.
  • Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
  • Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.

Responsibilities

  • Defines project scope, goals, and deliverables in collaboration with leadership.
  • Establishes measurable outcomes and evaluation criteria.
  • Determines and secures necessary resources for project success.
  • Independently plans, coordinates, and executes projects of moderate complexity and scope.
  • Manages full meeting life cycles—including agenda development, facilitation, and follow-up—to ensure effective outcomes.
  • Develops and refine workflows that improve coordination, efficiency, and compliance across teams.
  • Develops comprehensive project plans and timelines.
  • Validates schedules with impacted teams and adjusts for dependencies.
  • Tracks progress and implement corrective actions as needed.
  • Delegates tasks and ensures accountability across the team.
  • Conducts regular quality reviews of work and deliverables.
  • Maintains detailed and secure documentation of project activities.
  • Executes communication plans to keep stakeholders informed.
  • Prepares and delivers project updates and recommendations to leadership.
  • Establishes and continuously assesses the effectiveness of the internal controls within the unit and compliance with University policies and procedures.
  • Ensures employees are trained on controls within the function and on University policy and procedures.
  • Supports coordination and execution of clinical research process improvement initiatives, governance activities, grant support efforts (e.g., CCSG), and workflow standardization to advance research operations and institutional priorities.
  • Lead process improvement initiatives across clinical research operations by identifying gaps, inefficiencies and handoff breakdowns.
  • Partner with cross-functional stakeholders to implement streamlined, scalable process aligned with institutional goals.
  • Coordinate implementation of improved processes, including timelines and stakeholder alignment.
  • Monitor adoption and effectiveness of updated process, escalate risks or issues as needed.
  • Map current state and future state workflows to support standardization, transparency and improved operational consistency.
  • Support implementation of future state workflow.
  • Coordinate change management efforts by aligning stakeholders, clarifying expectations and supporting transition to standardized approaches.
  • Develop and maintain clear documentation, guidance materials and process references.
  • Facilitate working sessions to map workflows and incorporate feedback related to workflow changes.
  • Track readiness milestones to support smooth implementation and minimize operational disruption.
  • Act as a neutral facilitator to support alignment across departments with differing priorities during workflow changes.
  • Coordinate integration efforts across systems (e.g., OPERA, IBIS, Velos), ensuring alignment on scope, timelines, and dependencies.
  • Facilitate communication between technical teams, study teams, CRS groups, vendors, and internal stakeholders.
  • Track progress and escalate risks impacting system interoperability and delivery.
  • Coordinate governance-related activities, including committees focused on clinical research.
  • Facilitate meetings with leadership, and stakeholders across the institution to support alignment and decision-making.
  • Track deliverables and follow-up actions related to governance decisions and priorities.
  • Coordinate internal meetings to prepare for the Executive Advisory Board (EAB), including agenda development, materials preparation, and alignment with leadership priorities.
  • Document meeting outcomes, decisions, and action items, tracked follow up across stakeholders to ensure timely execution.
  • Serve as liaison between CRS leader and administration to support transparency and timely completion of drafts.
  • Maintain organized documentation of EAB materials.
  • Coordinate collection, validation, and consolidation of strategic plan metrics across Clinical Research, Administration, and institutional stakeholders.
  • Facilitate review of metrics with stakeholders to ensure accuracy, completeness, and alignment.
  • Track performance indicators and support identification of gaps, risks, and trends.
  • Support the development of reports, dashboards, and presentations that communicate progress against institutional goals.
  • Maintain alignment of metrics across Data Science, Shared Resources, and institutional reporting efforts.
  • Coordinate cross-functional and external initiatives (e.g., partnerships, pilot programs).
  • Facilitate alignment across internal teams and external partners to support execution of initiatives.
  • Track deliverables, participation, and outcomes across innovation efforts.
  • Facilitate meetings by guiding discussions, referencing project plans, and ensuring alignment on timelines, deliverables, and responsibilities.
  • Prepare and/or coordinate agendas and materials in advance to support effective discussions.
  • Capture and document meeting notes and action items, including key decisions, assigned owners, and required follow-ups.
  • Ensure documentation is complete, accurate, and clearly organized, reflecting all critical discussion points.
  • Review and validate notes prior to distribution to ensure quality and consistency.
  • Distribute meeting notes and action items within 24–48 hours.
  • Track action items, including ownership, due dates, and status.
  • Follow up with stakeholders between meetings to ensure progress and readiness for upcoming milestones.
  • Maintain organized and accessible documentation across projects, workflows, integrations, and reporting activities.
  • Ensure consistency, accuracy, and traceability of project-related information.

Benefits

  • medical
  • dental
  • tuition remission
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