Clinical Trials Lab Specialist II — Sample Management

Altasciences Company

Overland Park (KS)

On-site

USD 60,000 - 85,000

Full time

5 days ago
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Benefits offered by this job

Health/Dental/Vision
401(k) match
Paid Vacation & Holidays
Paid Sick & Bereavement Leave
Employee Assistance & Telehealth
Telework when applicable
Training & Development
Employee Referral Bonus Program

Job summary

Altasciences Company is seeking a Laboratory Specialist II to manage biological samples from clinical trials in a compliant, efficient manner. The role emphasizes strict adherence to protocol, GCP, and SOPs, with responsibilities including sample handling, data querying, and equipment maintenance.

The position requires strong communication, organization, and the ability to work in a fast-paced environment, with potential for mentoring junior staff and coordinating with external vendors.

Qualifications

  • High School Diploma or GED; college degree preferred.
  • 3–6 years of related experience.
  • Ability to read and interpret technical documents and manuals.
  • Ability to write advanced reports and correspondence.
  • Ability to speak effectively before groups of customers or employees.

Responsibilities

  • Ensure confidentiality and maintain a high level of quality within the department.
  • Report procedural deviations to supervisory team.
  • Understand protocol-driven timed study events and sample handling/processing.
  • Coordinate with external vendors (couriers, central lab).
  • Mentor Laboratory Specialist I team members.
  • Assist with maintaining equipment (freezers, refrigerators, centrifuges) and document accordingly.
  • Assist in the resolution of data queries.
  • Other tasks assigned by management.

Skills

Reading technical documents
Technical report writing
Verbal communication
Interpersonal skills
Multitasking
Initiative

Education

High School Diploma or GED
College degree preferred

Job description

Altasciences Company is seeking a Laboratory Specialist II to manage biological samples from clinical trials in a compliant, efficient manner. The role emphasizes strict adherence to protocol, GCP, and SOPs, with responsibilities including sample handling, data querying, and equipment maintenance.

The position requires strong communication, organization, and the ability to work in a fast-paced environment, with potential for mentoring junior staff and coordinating with external vendors.

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