Senior Coordinator-Research Compliance-Research Administration

Henry-Ford-Health-2; Detroit (MI); Sur place; USD 70 000 - 95 000; Plein temps

Résumé du poste

Henry Ford Health in Detroit, MI is seeking a Senior Coordinator for Research Compliance—Bioresources to ensure bioresources operations meet federal, state and institutional standards. You will coordinate animal care, tissue banking, specimen handling and prepare regulatory submissions to IACUC, IBC and other bodies.

You will develop SOPs, conduct audits, maintain records, train staff, and serve as the primary compliance liaison for research teams while monitoring regulatory changes and driving

Qualifications

• Requires 3–5 years in research compliance or bioresources management.
• Knowledge of USDA, NIH, FDA guidance.
• Experience with IACUC protocols preferred.
• Strong documentation and record-keeping skills.
• Proficiency with LIMS.

Responsabilités

• Coordinate compliance activities related to bioresources management.
• Develop and maintain SOPs aligned with regulatory requirements.
• Prepare regulatory documents and submissions to oversight bodies like IACUC and IBC.
• Conduct compliance audits and identify gaps with corrective actions.
• Maintain records and databases of biosource protocols and approvals.
• Serve as primary contact for research teams on compliance.
• Coordinate staff training on compliance policies.
• Monitor regulatory changes and communicate updates.
• Assist in preparation for review meetings and compliance presentations.
• Collaborate with coordinators and investigators to ensure seamless operations.
• Analyze data and generate reports to support improvements.

Connaissances

Regulatory knowledge

Documentation & reporting

Communication skills

Project management

Data analysis

IACUC knowledge

Biosafety protocols

Grant management

Audit/QA experience

Bioresources compliance

Outils

LIMS

Description du poste

Senior Coordinator-Research Compliance-Research Administration

At Henry Ford Health, we're committed to advancing health and improving lives for the millions of people we serve across Michigan and around the world. As one of the nation's leading academic health systems, we provide a comprehensive continuum of care that includes primary and preventive services, specialty and complex care, virtual care, pharmacy, home health, eye care, health insurance, and more. With 12 hospitals and hundreds of ambulatory care locations, including former Ascension Southeast Michigan and Flint Region facilities, our growing network expands access to exceptional care in the communities we serve.

Headquartered in Detroit, Henry Ford Health is helping shape the future of healthcare through the transformative Future of Health: Detroit initiative, a $3 billion investment that is redefining our academic healthcare campus and advancing innovation, research, education, and community impact.

Our work is grounded in purpose, collaboration, and belonging. We empower team members to grow their careers, contribute innovative ideas, and make a meaningful difference every day. Whether you're caring for patients, supporting operations, conducting research, or driving new solutions, you'll be part of a team united by a shared mission: delivering exceptional care, advancing health outcomes, and building healthier communities for all.

We're looking for a detail-oriented and organized Senior Coordinator for Research Compliance-Bioresources to join our team in Detroit, United States. In this role, you will serve as a key liaison between research teams, institutional leadership, and regulatory bodies, ensuring that all bioresources operations maintain the highest standards of compliance and ethical conduct. The ideal candidate will demonstrate exceptional organizational skills, a thorough understanding of research compliance frameworks, and a commitment to maintaining accurate documentation and regulatory adherence.

• Coordinate and oversee compliance activities related to bioresources management, including animal care, tissue banking, and biological specimen handling
• Develop, implement, and maintain standard operating procedures (SOPs) aligned with federal, state, and institutional regulatory requirements
• Prepare and submit regulatory documentation, reports, and applications to oversight bodies such as IACUC, Institutional Biosafety Committee (IBC), and other relevant agencies
• Conduct compliance audits and assessments to identify gaps and recommend corrective actions
• Maintain comprehensive records and databases related to bioresources protocols, approvals, and ongoing compliance activities
• Serve as a primary point of contact for research teams regarding compliance requirements and best practices
• Coordinate training programs and educational sessions on compliance policies and procedures for research staff
• Monitor changes in regulatory requirements and communicate updates to relevant stakeholders
• Prepare materials for institutional review meetings and compliance presentations
• Collaborate with research coordinators, principal investigators, and administrative staff to ensure seamless compliance operations
• Analyze compliance data and generate reports to support continuous improvement initiatives

• Minimum 3-5 years of experience in research compliance, bioresources management, or related regulatory field
• Demonstrated knowledge of federal and institutional research compliance regulations (USDA, NIH, FDA guidelines)
• Strong proficiency with documentation systems and laboratory information management systems (LIMS)
• Excellent written and verbal communication skills with the ability to explain complex compliance requirements clearly
• Advanced organizational and project management skills with the ability to manage multiple priorities simultaneously
• Proficiency in data analysis and the ability to generate comprehensive compliance reports
• Experience with IACUC protocols and animal care standards (preferred)
• Knowledge of biosafety protocols and biohazard handling procedures (preferred)
• Experience with grant management and regulatory submissions (preferred)
• Audit preparation and quality assurance experience (preferred)