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Project Senior Manager

Job in Ann Arbor, Washtenaw County, Michigan, 48113, USA
Listing for: Michigan Medicine
Full Time position
Listed on 2026-06-05
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Responsibilities

  • Milestone & Contract Management Tracking Deliverables (20%)
    • Maintaining detailed project workplans to achieve PCORI-specific contractual milestones on schedule.
    • Reporting execution: compiling and organizing semi-annual progress reports and milestone documentation, to be submitted to the PCORI Program Officer per contractual obligations.
    • Audit readiness: managing accurate recording of project data, regulatory approvals, and file systems to ensure institutional and federal compliance.
  • Clinical Research Operations (30%)
    • IRB coordination: preparing and submitting initial protocols, amendments, and continuing reviews to the Institutional Review Board (IRB).
    • Protocol support: developing and maintaining the protocol, Manual of Procedures, and all participant materials.
    • Data collection logistics: supporting the DCC in managing day‑to‑day data gathering workflow and ensuring adherence to the PCORI Methodology Standards.
    • Regulatory alignment: monitoring strict patient safety and data privacy safeguards across all active data collection arms.
    • Participant engagement: directing and carrying out the study's engagement plan, including support for patient stakeholders, in conjunction with study investigators.
    • Meeting support: organizing and directing study meetings as indicated.
  • Study Site Management (30%)
    • Site management: serving as the central hub for data‑gathering sites, subcontractors, and multi‑institutional collaborators, including maintaining relations with subcontractors, contracts management, and oversight of performance.
    • Clinical site performance: promoting successful recruitment, retention, and conduct at the study's clinical sites; supporting data entry, data quality, and other site activities; assuring that the highest rigor is applied to study conduct, data integrity, and research subject protection.
  • Financial & Resource Oversight (20%)
    • Budget reconciliation: collaborating closely with internal institutional finance departments to monitor spending against approved line items.
    • Invoicing & payments: supporting the DCC as needed with processing vendor, consultant, and subcontractor invoices per specific completed milestones.
    • Personnel allocation: managing Coordinating Center team members to maintain effective study functions per contractual obligations.
Required Qualifications
  • Bachelor's degree or equivalent combination of education and experience or 5 years of experience.
  • Strong analytical and problem‑solving skills with the ability to translate data into action.
  • Experience working with cross‑functional teams, including clinical stakeholders.
  • Excellent communication skills, with the ability to influence and engage diverse audiences.
  • Proven ability to manage competing priorities and operate effectively in ambiguity.
  • Proficiency in Microsoft Office (Excel, PowerPoint, Word).
  • Knowledge of UM policies and procedures.
Benefits
  • Excellent medical, dental and vision coverage effective on your very first day.
  • 2:1 match on retirement savings.
Equal Employment Opportunity Statement

The University of Michigan is an equal employment opportunity employer.

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Position Requirements
10+ Years work experience
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