WCG logo

IBC Specialist 1

WCG

Any City, USRemotePosted 1 day ago$19.50 - $28.10/hour
Full TimeEntry LevelOperations & Supply ChainCRO
Original posting ↗

Summary

Provide administrative support for the review of recombinant DNA research by an Institutional Biosafety Committee (IBC). Each IBC Specialist is paired with a Biosafety Analyst responsible for providing the scientific and professional support for the IBC review, and each team is assigned to specific clients and projects. Emphasis on data handling, tracking, organizational skills, and communication with internal and external clients.

Job description

Job Summary

Provide administrative support for the review of recombinant DNA research by an Institutional Biosafety Committee (IBC). Each IBC Specialist is paired with a Biosafety Analyst responsible for providing the scientific and professional support for the IBC review, and each team is assigned to specific clients and projects. Emphasis on data handling, tracking, organizational skills, and communication with internal and external clients.

Essential Duties/Responsibilities

  • Process client submissions for IBC Review.
  • Collect required documentation from clients as needed for IBC Review, Continuing Review and Closure.
  • Maintain continuing review records; follow up incomplete, inaccurate, or delinquent reports, obtaining supplemental information as necessary; provide complete and timely reports.
  • Maintain complete, accurate, and well-organized department files according to department standard.
  • Maintain client documents; create and maintain online meeting resources.
  • Correspond with members and clients to request meeting availability.
  • Attend meetings assigned and inscribe non-technical content meeting minutes.
  • Assist in recruiting external participants (e.g., consultants, committee members, and site inspectors); contribute to providing information to qualified candidates.
  • Collect required documentation from members and external maintain member files.
  • Prepare, complete, and track rosters for required submissions (e.g., to regulatory bodies or clients); prepare other similar reporting as necessary.
  • Communicate directly with corresponding personnel at regulatory bodies or clients to facilitate compliance with regulations and other agreements.
  • Distribute meeting notices and track responses, prepare agendas, prepare 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 both payables (external participants) and receivables (clients) for review and approval.
  • Serve as information and training resource for Support Staff.
  • Answer phones and screen correspondence; appropriately route inquiries according to department procedures.
  • Attendance and punctuality are essential functions of the position.
  • Other duties as assigned by supervisor.

Education Requirements

Associate degree (A.A.) or equivalent from two-year college or technical school and two years office experience supporting a member of an executive management team, or four years' related experience and/or training, or equivalent combination of education and experience.

Qualifications/Experience

  • Knowledge and proficiency in MS Office programs.
  • Must be quickly able to become proficient in new computer applications, and assist novice users.
  • Experience developing or working with databases is highly desirable.
  • Must not be debarred from participating in research.
  • Experience developing or working with databases and SharePoint is highly desirable.
  • Previous experience with IBCs or another research- or clinical-based regulatory operations a plus.

Travel Requirements: 0 - 5%

Requirements

  • Associate degree (A.A.) or equivalent from two-year college or technical school and two years office experience supporting a member of an executive management team, or four years' related experience and/or training, or equivalent combination of education and experience
  • Knowledge and proficiency in MS Office programs
  • Must be quickly able to become proficient in new computer applications, and assist novice users
  • Must not be debarred from participating in research
  • Experience developing or working with databases is highly desirable
  • Experience developing or working with databases and SharePoint is highly desirable
  • Previous experience with IBCs or another research- or clinical-based regulatory operations a plus

Benefits

  • Medical, Dental & Vision
  • Life & Disability Insurance
  • 401(k) Matching
  • Flexible Spending Accounts
  • Employee Assistance Programs
  • Referral Bonuses
  • Tuition Reimbursement
  • On-the-Job Training
  • Certification Assistance
  • Continuing Education Support
  • Paid Holidays
  • Vacation Time
  • Sick Time

Company overview

WCG is a leading clinical research organization (CRO) that specializes in accelerating and improving the clinical trial process through comprehensive solutions and technology-enabled services. Founded on a 55-year legacy as the pioneer of independent ethical review, WCG has evolved into a full-service partner for research sponsors, CROs, sites, and participants. The company operates globally with over 1,700 employees across 18 countries and supports approximately 95% of FDA-approved therapeutic agents. WCG's extensive service portfolio includes study planning and site optimization, patient identification and recruitment, scientific and regulatory review, data monitoring committees, endpoint adjudication, and pharmacovigilance services. The company leverages its proprietary WCG Knowledge Base™, which contains trusted data on 95% of all industry-sponsored protocols, to provide data-driven insights and benchmarking capabilities. WCG's innovative technologies, such as ClinSphere® Trial IntelX™, utilize AI-powered trial intelligence to predict outcomes and optimize clinical trial design. With deep relationships with over 2,800 research institutions including 195 academic medical centers, WCG serves as a critical partner in advancing clinical research across all therapeutic areas while ensuring compliance, quality, and patient safety throughout the clinical development lifecycle.

Explore more jobs of your matchFind more biopharma roles with GetBioJob.