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Laboratory Corporation of America Labcorp Clinical Trials Monitor in Town of Shelton, Connecticut

Labcorp is seeking a Clinical Trials Monitor to work in their Shelton, CT location. As the Clinical Trials Monitor, you will serve as a liaison between LabCorp, pharmaceutical companies and clinical investigators to provide technical assistance in the area of pharmaceutical clinical testing.

The schedule for this position is M-F 830a-5p.

Responsibilities Include:

  • Develop external laboratory worksheets, and help facilitate test code design.

  • Participate in meetings to trouble shoot issues with new and existing studies.

  • Other responsibilities include but are not limited to:

  • Coordinate workflow (staying on top of issues, follow up on delays)

  • Monitor turnaround time to ensure the established timeframe is met;

  • Work with all levels of laboratory personnel and pathology staff to answer inquiries and to help resolve problems;

  • Write and maintain Standard Operating Procedures and associated forms;

  • Accessioning of specimens and preparing specimens for laboratory testing;

  • Learning several LIS systems to perform data and result entry and verification;

  • Sample archiving and sample send outs;

  • Maintain a dashboard of all studies

Requirements

  • Bachelor's Degree in Biological Science.

  • 1-2 years of experience clinical laboratory experience preferred

  • Strong communication skills, both verbal and written

  • Someone who is detail oriented, organized, and has the ability to multi-task.

  • Strong computer skills, including excel and other Microsoft Tools

Shift

1

Schedule

1st Shift (Monday - Friday 9am - 5:30pm)

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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