Advarra

Sr Coordinator, Meeting Coordination

Advarra$66K — $116K *
US-AnywhereRemote in United States
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 2+ years of direct IRB experience along with a bachelor's degree or equivalent education/experience
  • CIP certification or ability to obtain it within one year
  • Advanced understanding of Federal laws on Human Subjects Research Protection
  • Proficiency in MS Word and Outlook

Responsibilities

  • Facilitate communication among Client Services, Board reviewers, and Clients
  • Prepare meeting and post-meeting informed consent forms (ICFs) incorporating Board feedback
  • Draft proposed meeting determinations for the Chair's review
  • Host web platforms for IRB meetings
  • Support Chairs and Board Members during meetings for regulatory compliance
  • Identify and resolve complex issues during IRB meetings
  • Collaborate with Client Services on IRB reporting of special issues
  • Conduct pre-reviews and quality checks on consent forms for compliance
  • Stay updated on U.S. and Canadian regulations regarding Human Subject Protections
  • Mentor new team members upon request

Benefits

  • Remote working opportunity within the U.S.
  • Participation in organizational training requirements
  • Opportunity to attend conferences, webinars, and workshops
  • Eligibility for health coverage and paid holidays
Full Job Description
Job Overview Summary

Manages the IRB meeting workflow by reviewing incoming submissions, assigning reviews to Board members, coordinating IRB meeting space/platform, and preparing informed consent forms (ICFs) in adherence to all applicable federal regulations.

Job Duties & Responsibilities

  • Facilitate communication between Client Services, Board reviewers, and Client

  • Prepare Meeting/Post meeting ICFs reflecting Board concerns and edits

  • Prepare proposed meeting determinations for Chair review

  • Host web platform for IRB meetings

  • Provide pre-and during-meeting support to Chairs and Board Members for regulatory compliance

  • Manage complex issues arising during IRB meetings

  • Identify and address issues needing attention by the IRB and Chair

  • Challenge or clarify opinions and questions during IRB meetings

  • Collaborate with client services on reporting special issues to the IRB

  • Analyze and recommend improvements to IRB review methods

  • Conduct accurate pre-reviews of consent forms for regulatory compliance

  • Edit consent forms to align with regulatory standards and Advarra operational guidelines

  • Apply negotiated language to consent forms as per client agreements

  • Collaborate with stakeholders to incorporate necessary edits

  • Perform quality control checks on consent forms

  • Stay updated on U.S. and/or Canadian Regulations and Guidelines in Human Subject Protections and research areas

  • Complete standard Human Subjects Research Training, e.g., CITI, as per management's cycle

  • Fulfill organizational training requirements

  • Attend conferences, webinars, workshops as agreed upon with management

  • Manage IRB meetings weekly on average over additional Board meetings as requested by management

  • Mentor new team members upon request


Location

This role is open to candidates working remotely in the United States.

Basic Qualifications

  • 2+ years IRB experience in addition to a bachelor's degree; or a combination of education and experience

  • Certified IRB Professional (CIP) or attainment of CIP within one (1) year of eligibility


Preferred Qualifications

  • Advanced knowledge of Federal laws and guidelines pertaining to Human Subjects Research Protection

  • Proficient with MS Word and Outlook


Physical and Mental Requirements

  • Sit or stand for extended periods of time at stationary workstation

  • Regularly carry, raise, and lower objects of up to 10 Lbs.

  • Learn and comprehend basic instructions

  • Focus and attention to tasks and responsibilities

  • Verbal communication; listening and understanding, responding, and speaking


Pay Transparency Statement
The base salary range for this role is $66,767 - $116,089. Note that salary may vary based on location, skills, and experience and may vary from the amounts listed above. This position may also be eligible for a variable bonus in addition to base salary as well as health coverage, paid holidays, and other benefits.

About Advarra

Advarra is a leading provider of institutional review board (IRB), institutional biosafety committee (IBC), and research quality and compliance consulting services to the healthcare industry. The company helps healthcare organizations and research institutions navigate the complex regulatory landscape of clinical research, ensuring that their studies are conducted ethically and in compliance with all applicable laws and regulations. Advarra was founded in 2017 and is headquartered in Columbia, Maryland. The company has over 1,000 employees and serves clients across the United States and internationally. Advarra is committed to advancing the field of clinical research and improving patient outcomes through its innovative solutions and services.
Learn more about Advarra
Size
1,000 employees
Industry
Founded
2017

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