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Weekend Irb Jobs in Michigan (NOW HIRING)

McLaren

Coordinator Clinical Research

Flint, MI · On-site

$23.50 - $31.25/hr

Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO. 7. Assists the investigators and clinicians in identifying and ...

Spectrum Health

Research Assistant

Royal Oak, MI · On-site

$18 - $24.75/hr

Dealing with IRB regulatory issues. Supporting manuscript and grant development, and submission ... Days Worked Monday-Friday Weekend Frequency N/A CURRENT COREWELL HEALTH TEAM MEMBERS - Please apply ...

Michigan Medicine

Clinical Research Coord Assoc

Ann Arbor, MI · On-site

$23.75 - $31.50/hr

Completes IRB applications and associated documentation with PI support. Collaborate swith clinical decision support teams and stakeholders to ensure consistent system standards. Required ...

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Weekend Irb information

What is a weekend IRB?

Weekend IRB jobs refer to positions related to Institutional Review Boards (IRBs) that operate or require work during weekends. IRBs are committees established to review and approve research involving human subjects, ensuring ethical standards are met. Weekend IRB staff may include coordinators, administrators, or reviewers who process submissions, review protocols, and ensure compliance outside of normal weekday hours to accommodate researchers' needs and deadlines.

What are the typical responsibilities of a weekend IRB member?

As a Weekend IRB (Institutional Review Board) member, your primary responsibility is to review research protocols submitted for ethical and regulatory compliance, particularly those requiring urgent or expedited consideration over weekends. This role often involves collaborating remotely with fellow board members, principal investigators, and compliance staff to ensure timely feedback on submissions. Challenges may include balancing multiple protocols with tight deadlines and maintaining clear communication despite limited in-person interaction. Your input directly impacts participant safety and institutional compliance, making attention to detail and ethical judgment essential.

What are the key skills and qualifications needed to thrive as a weekend IRB member?

To thrive as an IRB member, you generally need a background in research ethics, regulatory compliance, and relevant academic or clinical experience, often supported by advanced degrees in health, law, or social sciences. Familiarity with federal regulations (such as 45 CFR 46), online protocol management systems, and human subjects protection certifications (e.g., CITI Program) is typically required. Strong analytical thinking, attention to detail, impartiality, and effective communication skills distinguish outstanding IRB members. These skills ensure that research protocols are ethically reviewed, participant rights are protected, and institutional compliance is maintained.

What is the difference between Weekend IRB vs IRB Coordinator?

AspectWeekend IRBIRB Coordinator
CertificationsOften requires IRB-related training, but not always formal certificationsTypically requires IRB or research compliance certifications
Work EnvironmentPart-time, flexible hours, often on weekends or eveningsFull-time, office-based, regular weekday schedule
Employer & IndustryResearch institutions, hospitals, universitiesResearch institutions, hospitals, universities

Weekend IRB roles focus on providing oversight during non-standard hours, often with flexible schedules, while IRB Coordinators handle ongoing compliance, documentation, and communication during regular hours. Both roles are essential in research oversight but differ mainly in work hours and specific responsibilities.

How to get a Weekend IRB job?

To get a Weekend IRB job, candidates should have relevant experience in research or clinical settings, often requiring knowledge of regulatory compliance and ethical review processes. Strong organizational skills and the ability to work independently during weekends are important. Applying through job boards, networking within research institutions, and obtaining certifications like GCP can improve chances.

What are the most commonly searched types of Irb jobs in Michigan?

The most popular types of Irb jobs in Michigan are:

Weekend Irb jobs near you

Sr Coor-Research Compliance- Full time - Research Administration

Detroit, MI • On-site

Henry Ford Health System
51 - 200 employees
Learn more about Henry Ford Health Systemexternal

Full-time

Re-posted 8 days ago

Job description

GENERAL SUMMARY: 

  • Research Compliance is centralized to Research Administration at the main campus. 
  • The Senior Coordinator-Research Compliance has administrative responsibility for our institutional research compliance committee(s). 
  • The position is responsible for ensuring that Henry Ford Health research activities comply with federal, state, local, regulatory agencies, and Henry Ford Health regulations and policies for the conduct of research involving animal and human studies. 
  • The position ensures the efficient committee operations that include writing meeting agendas, recording minutes, writing correspondence, maintaining quality data in the compliance database, and monitoring approval period lapses. 
  • This individual generates information that is reported out to departments, the committee(s), and Henry Ford Medical Group (HFMG) leadership.
  •  The position is knowledgeable of federal agency, state, local, and Henry Ford Health guidelines, and ensures that this information is disseminated out to the research community. 
  • Also responsible for ensuring that the appropriate training occurs for researchers and committee members as required by federal regulations.
  •  Develops and/or implements education modules, standard operating procedures, and policies for the research community. 

EDUCATION/EXPERIENCE REQUIRED:

  • Bachelor's degree in compliance, health sciences, health related field, or business. 
  • Master's Degree preferred. 
  • Preferred Qualifications: 
  •  In depth knowledge of: OHRP / Common Rule (45 CFR 46); FDA regulations (21 CFR 50, 56); HRPP / AAHRPP standards  
  • Direct IRB administration experience
  • Multi-committee exposure (highly valuable at HFH) to IRB + IACUC + IBC/Biosafety familiarity & Understanding of cross-committee coordination and dependencies.
  • Systems experience of IRB platforms (IRBNet, eIRB systems, etc)
  • Preferred Credentials:  CIP (Certified IRB Professional) , CHRC (Certified in Healthcare Research Compliance) or working toward it
  • Comfortable working in High-volume, complex academic healthcare system with a mix of: Investigator-initiated research, Industry-sponsored trials, and Increasing cross-institutional work (e.g., MSU integration, reliance models)

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