Hire Partnership - Boston, MA

posted 5 months ago

Full-time - Entry Level
Remote - Boston, MA
Administrative and Support Services

About the position

We are seeking a detail-oriented Clinical Research Systems Specialist (CRSS) to lead the activation and management of clinical trials, ensuring accuracy in documentation and compliance with regulatory standards. This role is fully remote, but candidates must reside in Massachusetts. The CRSS will work Monday to Friday from 9 AM to 5 PM, with a pay range of $23 to $25 per hour. The position is temporary with the potential to become permanent, depending on performance and organizational needs. In this role, the CRSS will be responsible for subject registration, which includes randomizing and registering clinical trial subjects while ensuring data quality and compliance with established protocols. The CRSS will also be tasked with quality control of the OnCore Clinical Trial Management System (CTMS), reviewing and maintaining accurate data, and monitoring and resolving any quality control errors that may arise. Additionally, the CRSS will facilitate protocol activation and management, which involves activating and amending protocols in the iRIS system and conducting compliance and readiness reviews. Training and support for new specialists will also be a key responsibility, where the CRSS will provide input on work instructions and system changes to enhance operational efficiency. Strong written and verbal communication skills are essential for success in this role, as is a meticulous attention to detail.

Responsibilities

  • Randomize and register clinical trial subjects.
  • Ensure data quality and compliance with clinical trial protocols.
  • Review and maintain accurate data in the OnCore CTMS.
  • Monitor and resolve quality control errors.
  • Facilitate activation and amendments of protocols in iRIS.
  • Conduct compliance and readiness reviews for clinical trials.
  • Help train new specialists and provide input on work instructions and system changes.

Requirements

  • Associates degree or equivalent experience (Bachelor's preferred).
  • 1 year of experience in clinical trials.
  • 1 year of experience in research.
  • Strong written and verbal English communication skills.
  • Basic knowledge of clinical trial regulations and systems.
  • Ability to work independently.

Nice-to-haves

  • Experience in medical/scientific research preferred.
  • Meticulous attention to detail.
  • Strong communication skills.

Benefits

  • Health insurance
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service