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WCG Clinical

Clinical trial management services and technologies

IBC Specialist 1

Administrative SupportPosted on Nov 11
Full-timeRemote in USA$19.50 - $28.10 /hr

About the Job

Requirements

  • An associate degree or equivalent from a two-year college or technical school and two years of office experience supporting a member of an executive management team; alternatively, four years of related experience and/or training, or an equivalent combination of education and experience.
  • Knowledge of and proficiency in Microsoft Office programs.
  • Ability to quickly become proficient in new computer applications and assist novice users.
  • Must not be debarred from participating in research.

Responsibilities

  • Process client submissions for Institutional Biosafety Committee (IBC) review.
  • Collect required documentation from clients for IBC review, continuing review, and closure.
  • Maintain continuing review records; follow up on incomplete, inaccurate, or delinquent reports; obtain supplemental information as necessary; and provide complete and timely reports.
  • Maintain complete, accurate, and well-organized department files according to department standards.
  • Maintain client documents and create and maintain online meeting resources.
  • Correspond with members and clients to request meeting availability.
  • Attend assigned meetings and record non-technical meeting minutes.
  • Assist in recruiting external participants, including consultants, committee members, and site inspectors, and provide information to qualified candidates.
  • Collect required documentation from members and maintain member files.
  • Prepare, complete, and track rosters for submissions to regulatory bodies or clients, and prepare similar reports as needed.
  • Communicate directly with personnel at regulatory bodies or clients to facilitate compliance with regulations and other agreements.
  • Distribute meeting notices and track responses; prepare agendas and ensure distribution of meeting information.
  • Prepare and coordinate distribution of final signed minutes, letters, reports, and other documents.
  • Verify billing accuracy and prepare invoices for external participant payables and client receivables for review and approval.
  • Serve as an information and training resource for support staff.
  • Answer phones, screen correspondence, and route inquiries according to department procedures.
  • Meet attendance and punctuality requirements.
  • Perform other duties as assigned by the supervisor.

Desired Qualifications

  • Experience developing or working with databases.
  • Experience developing or working with databases and SharePoint.
  • Previous experience with IBCs or other research- or clinical-based regulatory operations.

About the Company

WCG Clinical

Clinical trial management services and technologies

WCG Clinical provides a suite of services and technologies to streamline clinical research for pharma, research organizations, and institutions. It covers ethical review, site administration, patient recruitment, quality management, and training solutions, built through acquisitions (PharmaSeek, The Avoca Group, MedAvante, Array) to cover the full trial workflow. The platform delivers integrated, end-to-end capabilities across the trial lifecycle—from ethics approvals to patient engagement and training—to run studies more efficiently and cost-effectively. Its goal is to reduce time and cost to bring new medical treatments to market by improving clinical research efficiency and effectiveness.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
West Windsor Township, NJ
Founded
1968

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