The Healthcare Research IT Project Manager plays a pivotal role in leading and coordinating clinical research informatics and data acquisition projects. Reporting to the Portfolio Manager, this position bridges the gap between clinical researchers, data scientists, and technical stakeholders. The ideal candidate will have a strong background in project management within healthcare or research informatics environments and a keen understanding of data governance, research regulations, and interoperability standards.
Job Responsibilities:
Lead the planning, execution, reporting, and closeout of clinical research informatics projects
Facilitate communication between clinical researchers, data scientists, and project teams
Provide management and oversight for projects supporting the Health Data Informatics and Research team
Ensure project compliance with regulatory, fiscal, and contractual requirements
Support Bio Data Catalyst program planning and reporting, ensuring milestone and deliverable alignment
Coordinate stakeholder meetings, including drafting agendas, documenting meeting minutes, and tracking action items
Assist in the preparation of internal and external reports including status updates and strategic reviews
Manage cross-functional teams and multiple concurrent projects in a matrixed research environment
Compose both scientific and business communications for stakeholders, including university leadership
Ensure security, compliance, and privacy (HIPAA, IRB) for cloud-based research data management solutions
Track and communicate status updates to all internal and external project stakeholders
Apply standard project management practices and tools to ensure consistency and transparency
Required Skills:
Minimum 5 years of experience in health informatics project management
Experience working with or in a Healthcare IT Project Management Office
Proficiency in project tools such as MS Project, MS Excel, MS Teams, MS Word, and MS Visio
Proven experience building business cases and ROI documentation
Strong understanding of EMRs and electronic data capture systems
Deep understanding of business requirements gathering and regulatory compliance for research
Bachelor’s degree in a related field
Excellent written and verbal communication skills
Ability to manage diverse, cross-functional teams and stakeholders
Familiarity with virtual/cloud-based data management with secure and compliant configurations
Preferred Skills:
Understanding of clinical trials research and workflows
Budget management experience in a research environment
Experience in an academic medical setting
Familiarity with HL7 CDA and FHIR interfaces
Knowledge of Cerner EMR system
Familiarity with ICD, CPT, LOINC, MedDRA ontologies
Experience with OMOP/OHDSI tools and REDCap
Experience working with AWS and related data solutions
Certifications:
[Specify if any certifications are required or preferred – e.g., PMP, CPHIMS]
Remote or Onsite:
[Specify: Remote / Hybrid / Onsite with details on location and travel requirements