Operations Manager, Clinical Assessment Technologies

Worldwide Clinical Trials

Kansas City (KS)

On-site

USD 90,000 - 178,000

Full time

8 days ago
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Job summary

Worldwide Clinical Trials is seeking an Operations Manager to oversee rater selection, rater certification/qualification, rater training content, scale acquisition, surveillance maintenance, and workbook/source document management for Worldwide Clinical Trials, Inc. (Worldwide).

The Operations Manager is responsible for ensuring all projects are conducted timely and in compliance with SOPs, ICH/GCP, and regulatory guidelines.

Qualifications

  • Bachelor’s degree in Life Science preferred.
  • 2–4 years of experience working in clinical trials.
  • At least 2 years' experience managing team members or leading a team.
  • Knowledge of SOPs, ICH/GCP and regulatory guidelines.
  • Fluency in English for day-to-day business.

Responsibilities

  • Coordinate completeness of rater experience qualification documents and communicate results to Sponsor and study team.
  • Develop study-specific rater training portals and ensure readiness based on study timelines.
  • Coordinate Investigators’ Meetings and CAT materials; may attend such meetings.
  • Oversee editing/formatting of didactic training presentations.
  • Oversee scale licenses, translations, regulatory authorizations, and Sponsor approvals.
  • Maintain data surveillance by tracking and reconciling source documentation and providing reports.

Skills

Team leadership
Project management
Time management
Verbal communication
MS Office

Education

Bachelor’s degree in Life Science

Tools

Microsoft Word
Excel
Adobe
PowerPoint

Job description

Worldwide Clinical Trials is seeking an Operations Manager to oversee rater selection, rater certification/qualification, rater training content, scale acquisition, surveillance maintenance, and workbook/source document management for Worldwide Clinical Trials, Inc. (Worldwide).

The Operations Manager is responsible for ensuring all projects are conducted timely and in compliance with SOPs, ICH/GCP, and regulatory guidelines.

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