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HealthPartners

Integrated health system and health plans

Research Project Manager

Medical ResearchConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A Master's degree in a health-related field; a PMP or ACRP-CRC certification plus some experience, or five or more years of relevant professional expertise, may be substituted for lesser academic degrees.
  • Specialized training for the study-specific area(s) of expertise.
  • A minimum of three years of experience recruiting for, implementing, and monitoring research projects, including data-only and human subjects studies.
  • Demonstrated planning and management skills.
  • Ability to adhere to a research protocol while exercising sufficient flexibility and judgment to handle unforeseen situations.
  • Excellent written and verbal communication skills.
  • Ability to establish and maintain effective relationships with care providers and operations/support staff, study participants, and outside funders and sponsors.
  • Experience developing and maintaining computerized databases.
  • Reliable transportation for travel to HealthPartners clinics and meeting sites.

Responsibilities

  • Manage complex research studies using a thorough understanding of project objectives and serve as a consultant and facilitator for areas requiring specific expertise.
  • Manage projects within established grant operating budgets, coordinate recruitment and data collection, conduct qualitative interviews, advise principal investigators on protocol content and implementation systems, and direct participating staff as needed.
  • Coordinate one or multiple projects, including data-only, human subjects, sub-site, and survey studies; liaise with clinic staff and internal and external departments, companies, and grant partners; facilitate groups, meetings, and committees; and support more experienced project managers in paired models on complex studies when needed.
  • Develop detailed project plans, timetables, and resource estimates and track progress to meet deadlines with consideration of the scientific nature of the project.
  • Contribute to protocols, manuals of procedures, required regulatory documentation, and Clinical Trials submissions.
  • Collaborate with internal and external sources to design documentation systems, forms, questionnaires, and surveys; act as the main contact for external collaborators when needed.
  • Identify and address barriers to success independently and develop plausible solutions to complex problems.
  • Implement study protocols and ensure compliance with regulatory guidelines.
  • Direct study staff work, including training and evaluation when applicable, and educate staff on organizational and regulatory policies and procedures.
  • Allocate and coordinate resources, maintain budgets for studies with large budgets and complex financial situations, and contribute to operational feasibility analysis when needed.
  • Design and oversee data collection processes; develop and implement methods to assess data accuracy and completeness; document collection processes; and maintain orderly working and project files.
  • Conduct focus groups, summarize interviews, and participate in qualitative analysis.
  • Conduct open-ended interviews with probes and draft intervention materials when needed.
  • Manage, implement, and conduct project interventions.
  • Create reports and perform basic statistical analysis of results as requested.
  • Draft or develop Institutional Review Board applications for data-only studies or develop human-subject materials for Institutional Review Board submissions.
  • Contribute to periodic and final reports for funding agencies and oversight organizations and serve as primary contact for the Institutional Review Board and funding agencies when needed.
  • Participate in presentations and draft abstracts or posters when requested.
  • Participate in writing journal articles.
  • Draft regulatory applications to conduct research.
  • Participate in research operations and other HealthPartners Institute activities.
  • Perform miscellaneous research tasks as assigned.
  • Manage contract development with consultants and sub-recipients as needed or delegated by the Principal Investigator.
  • In collaboration with study investigators and Research Project Management Office supervisors, consult necessary personnel about issues affecting the department and study, including recurring clinical problems and inaccessible resources.
  • Coordinate and manage complex research studies involving relationship issues and responsibility for decisions about implementation and report authoring; oversee and track study-related activities of study staff.

Desired Qualifications

  • Two years of experience in staff supervision.
  • Four years of experience in health care or research.
  • Specialty training or expertise in a research-related area.

About the Company

HealthPartners

Integrated health system and health plans

HealthPartners is an integrated health care organization that provides medical and dental care alongside health plan financing and administration. Its care system combines a multi-specialty physician network with health plans so members receive coverage and services within one organization. It differs from competitors through its nonprofit, consumer-governed structure and its large, in-house delivery system, which supports coordinated care under one umbrella. The goal is to improve the health of members and communities by offering affordable, accessible, and comprehensive health care and insurance.

Company size
5,001-10,000
Company stage
Debt Financing
Total funding
$116M
Headquarters
Bloomington, MN
Founded
1957

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