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Research Finance Specialist - Pre-Award

Job in Minneapolis, Hennepin County, Minnesota, 55401, USA
Listing for: Minneapolis Heart Institute Foundation
Full Time position
Listed on 2026-07-19
Job specializations:
  • Research/Development
    Regulatory Compliance Specialist, Clinical Research
Job Description & How to Apply Below
Position: Research Finance Specialist I - Pre-Award

Where Purpose Meets Progress

At the Minneapolis Heart Institute Foundation (MHIF), your work unlocks new knowledge, supports patient-centered care, and advances cardiovascular research and education. As a Research Finance Specialist 1 – Pre-award, you'll do more than support studies—you'll help propel a mission that changes and saves lives.

Summary

The Research Finance Specialist 1 – Pre-award supports operational, financial, regulatory, and system-related activities required for clinical research study start-up and activation. This role is responsible for coordinating and supporting pre-award activities across the clinical research lifecycle, including study intake, feasibility review, study start-up coordination, coverage analysis, budget development, contract support, document consistency review, and CTMS builds.

Primary Responsibilities
  • Support intake and start-up activities for clinical research studies across industry-sponsored and investigator-initiated programs.
  • Coordinate and track study start-up workflows, activation timelines, and required approvals to support efficient study implementation.
  • Support operational, financial, and research feasibility assessments in collaboration with investigators, study teams, and operational stakeholders.
  • Assist in validation of coverage analysis reviews by evaluating clinical protocols, informed consent forms, budgets, contracts, and related study documents to determine billable versus sponsor-funded items and services.
  • Assist in developing study billing grids, billing designations, and research financial workflows to support research billing compliance and operational readiness.
  • Assist in developing clinical trial budgets, pricing reviews, and financial assessments in partnership with study teams, ancillary departments, organizational stakeholders and 3rd party partners.
  • Support budget negotiations and financial discussions with sponsors and Clinical Research Organizations (CROs) in collaboration with research administration and contracting teams.
  • Assist in reviewing and coordinating research agreements, including Clinical Trial Agreements (CTAs), Confidentiality Agreements (CDAs), subcontracts, and related research documents.
  • Collaborate with legal, compliance, finance, and operational teams to support contract execution workflows and ensure consistency among study budgets, contracts, and operational requirements.
  • Perform quality review of study documents and research systems to ensure consistency across protocols, informed consent forms, budgets, contracts, coverage analyses, regulatory documentation, and research systems.
  • Identify discrepancies, documentation gaps, billing risks, or funding concerns and communicate findings to appropriate stakeholders.
  • Support research study build activities within Clinical Trial Management Systems (CTMS), financial systems, and related operational platforms, including workflow validation and issue resolution.
  • Coordinate with IT, research administration, billing, and operational teams to support accurate system configuration and downstream financial and compliance processes.
  • Maintain organized study documentation, tracking tools, and activation records to support audit readiness and institutional compliance requirements.
  • Facilitate communication between internal stakeholders and external sponsors, CROs, and partner organizations regarding study activation requirements, contracting milestones, and operational readiness.
  • Participate in process improvement initiatives designed to enhance research operations, compliance, and study start-up efficiency.
  • Partner with key stakeholders to ensure compliance with CMS, FDA, HIPAA, Good Clinical Practice (GCP), and institutional research requirements.
  • Other duties as assigned – this position may support other functions as required by business need. This job description represents the major functions of the position but is not intended to be all-inclusive.
Relationships

This role reports to the Director of Research Finance Operations. Frequent interactions with investigators, Clinical Research Coordinators (CRCs), Research Managers, compliance and finance. Works closely with Allina Office of…

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