About The Position

The Coordinator II, Client Services is responsible for providing exemplary client service and serves as the main point of client contact for designated pharmaceutical companies, contract research organizations, and academic medical centers. This position will provide direct client assistance and advisement to facilitate IRB review and translate IRB decisions and processes to clients to maintain continuity and timely communications.

Requirements

  • Two (2) years’ experience in IRB or clinical research setting that includes applying regulations to the protection of human subjects.
  • Intermediate computer skills, including proficiency with MS Office Suite with an emphasis on Word and Outlook
  • Ability to effectively use proprietary system

Nice To Haves

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

Responsibilities

  • Serve as the main Sponsor, CRO and PI site, contact on assigned studies
  • Assist with other studies as needed and serve as a primary Sponsor, CRO and PI site contact on submissions that are assigned to you
  • Conduct administrative review of Protocol/site submissions by reading, reviewing, and understanding protocol requirements and all supporting documentation
  • Demonstrate advanced understanding of multiple types of Protocol and Site Submissions
  • Document and execute client customizations as requested; process change requests for approved Protocols
  • Manage vendor relations and documentation for foreign language translations
  • Maintain a high level of accuracy and attention to detail; collaborate with the quality assurance team to ensure minimal rate of error
  • Complete work in a timely manner, responding to customers within 24 hours of email/voicemail receipt
  • Escalate any customer or timeline issues to management

Benefits

  • health coverage
  • paid holidays
  • variable bonus
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