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Irb Manager Part Time Jobs (NOW HIRING)

The Pennsylvania State University

$18/hr

Collect self-report survey data and manage wearable data (e.g., fitness tracker output) * Enter ... with IRB documentation and compliance tracking * Perform other research-related activities as ...

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How much do irb manager part time jobs pay per year?

As of Jun 20, 2026, the average yearly pay for irb manager part time in the United States is $78,591.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,000.00 and $81,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an IRB Manager (Part Time), and why are they important?

To thrive as an IRB Manager (Part Time), you need in-depth knowledge of federal regulations for human subjects research, experience in research compliance, and typically a bachelor’s or master’s degree in a related field. Familiarity with electronic IRB management systems and certifications such as CIP (Certified IRB Professional) are highly valuable. Exceptional organizational skills, attention to detail, and strong interpersonal communication are crucial soft skills for success in this role. These skills ensure ethical oversight, regulatory compliance, and effective coordination between researchers and the Institutional Review Board.

What jobs pay 2000 a day?

IrB Managers in part-time roles typically do not earn $2,000 a day, as such high daily rates are uncommon in this field. High-paying jobs that can reach this level often include specialized consulting, executive roles, or freelance work in industries like finance, law, or technology, which require advanced skills and experience. These positions usually involve significant responsibility, expertise, and sometimes self-employment or contract work.

Who hires the most project managers?

Large organizations across industries such as technology, construction, healthcare, and finance typically hire the most project managers. These companies often have ongoing projects requiring coordination, planning, and management skills, making project management roles prevalent in their staffing needs.

How to get a job on an IRB?

To become an IRB manager part-time, candidates typically need a background in research ethics, healthcare, or related fields, along with experience in regulatory compliance. Relevant certifications such as IRB or research ethics training can enhance prospects, and strong organizational and communication skills are essential for managing IRB processes effectively.

What does an IRB manager do?

An IRB manager oversees the Institutional Review Board's review process for research involving human subjects, ensuring compliance with ethical standards and federal regulations. They coordinate protocol submissions, facilitate meetings, and maintain documentation to protect participant rights and safety.

What does an IRB Manager do in a part-time role?

An IRB (Institutional Review Board) Manager in a part-time role oversees the review and approval process for research involving human subjects to ensure compliance with ethical standards and federal regulations. Their responsibilities typically include coordinating IRB meetings, reviewing research protocols, ensuring proper documentation, and providing guidance to researchers. Even part-time IRB Managers play a crucial role in safeguarding participant rights and maintaining research integrity, often balancing administrative duties with regulatory compliance tasks.

What are some common challenges faced by part-time IRB Managers when balancing compliance oversight with limited hours?

Part-time IRB Managers often encounter the challenge of maintaining thorough oversight of research protocols and ensuring timely review processes within a reduced work schedule. Effective time management and prioritization are essential, especially during periods of high submission volume or when new regulations are introduced. Frequent communication and clear delegation with IRB staff and committee members help maintain workflow continuity. Staying organized and leveraging digital management tools can also support compliance and efficiency despite limited hours.
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Irb Manager Part Time jobs near you
Infographic showing various Irb Manager Part Time job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 95% Full Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $78,591 per year, or $37.8 per hour.
Clinical Research Regulatory Administrator

Clinical Research Regulatory Administrator

Mangrove Management Partners

Burlington, MA • On-site

$60K - $65K/yr

Part-time

Posted 24 days ago

Job description

Clinical Research Regulatory Administrator
Overview
Vascular Breakthroughs supports clinical trials for a growing group of vascular surgeons. This role provides administrative and regulatory support to keep study documentation current, ensure staff training compliance, support IRB submissions, and maintain required trial files and systems.
This role is a hybrid, with a combination of in-person and remote work. Periodic travel is required between offices to perform job duties.
Responsibilities
  • Keep provider CVs current and compliant for all Principal Investigators and Sub-Investigators
  • Ensure signatures are current in RealTime
  • Maintain all medical licenses (MLs) in RealTime
  • Manage Good Clinical Practice (GCP) and Human Subjects training for all staff
  • Manage provider CME tracking and American College of Surgeons credentialing requirements
  • Assist with onboarding new staff for clinical research, including:
    • Collect MLs and CVs
    • GCP and HR training
    • Electronic signatures
    • Training for all current studies
  • Assist with gathering regulatory documents for new trials and attend training sessions as needed
  • Assist providers with ensuring regulatory signatures are current in RealTime (may require travel between offices)
  • Document clinical oversight meetings to demonstrate ongoing oversight
  • Assist with filing regulatory documents with the IRB, including:
    • Submissions for new studies
    • Annual submissions for current studies
  • Maintain Trial Master File (TMF) for investigator-sponsored trials (regulatory requirement)
  • Support monitoring activities for investigator-sponsored trials
  • Develop and maintain SOPs, including validation updates of RealTime software
  • Transcribe data from RealTime to the Electronic Data Capture (EDC) system used by trials

Qualifications/Requirements
  • Bachelor's degree (or in-progress degree completion) in life sciences, health sciences, public health, business administration, or a related field preferred
  • 0-2 years of relevant experience (internship, co-op, or part-time work) in healthcare administration, clinical research, regulatory coordination, or a related environment preferred
  • Strong attention to detail and ability to maintain accurate documentation, version control, and audit-ready files
  • Excellent organizational and time-management skills; able to manage multiple tasks and deadlines across studies and sites
  • Clear written and verbal communication skills; comfortable following up with providers and staff to obtain required documents and signatures
  • Comfort with learning new systems and software platforms (e.g., document management, training tracking, EDC/CTMS tools); proficiency with Microsoft Office
  • Ability to work independently while also collaborating with a distributed team across multiple practice locations
  • Reliable transportation and willingness to travel between offices as needed (reimbursed)

Compensation
$60,000 - $65,000 per year. Negotiable based on skills and experience.
#Mangrove

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