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Altasciences

Integrated CRO for early-phase drug development

Laboratory Specialist 2

Clinical Research OperationsPosted on Nov 9
Full-timeOverland Park, KS, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or GED is required; a college degree and related work experience are preferred.
  • A minimum of 3–6 years of related experience is required.
  • Ability to read and interpret technical documents and industry-specific manuals.
  • Ability to write advanced reports and correspondence.
  • Ability to speak effectively before groups of customers or employees of the organization.
  • Excellent verbal and written communication skills.
  • Well-developed interpersonal skills.
  • Personal and professional integrity and discretion in handling confidential information.
  • Ability to develop trusting relationships to gain support and achieve results.
  • Ability to manage multiple conflicting priorities.
  • Self-direction, motivation, and initiative to identify and anticipate study needs and recommend implementations to management.
  • Attention to detail, organization, customer service focus, and ability to work in a fast-paced environment.
  • Ability to work overtime, holidays, weekends, and evening hours as needed.
  • Must be legally authorized to work in the United States and possess valid work authorization that does not require employer sponsorship now or in the future.

Responsibilities

  • Process biological samples collected during clinical trials and assist with their management while ensuring compliance with study protocols, Good Clinical Practices, and Standard Operating Procedures.
  • Protect the confidentiality of clinical trial participants and sponsors while maintaining departmental quality.
  • Report procedural deviations, issues, and problem resolutions to appropriate supervisory team members.
  • Understand protocol-driven timed study events, including centrifugation, study and clinical diagnostic sample handling and processing, sample storage, and acceptable time windows prescribed by protocol or Standard Operating Procedures.
  • Coordinate with external vendors, including shipment couriers and central laboratories.
  • Mentor Laboratory Specialist I team members.
  • Assist with maintaining sample-management equipment, including freezers, refrigerators, and centrifuges, and document maintenance accordingly.
  • Assist with resolving data queries.
  • Perform other tasks assigned by management.

Desired Qualifications

  • A college degree and related work experience.

About the Company

Altasciences

Integrated CRO for early-phase drug development

Altasciences provides integrated early-stage drug development services, covering preclinical testing, early clinical trials, and contract manufacturing. It functions as a single, in-house CRO that coordinates discovery support, safety testing, clinical research, and manufacturing to streamline a program from start to early proof of concept. The company differentiates itself by offering an end-to-end, one-stop path rather than requiring clients to contract multiple vendors. Its goal is to help innovator programs move quickly and efficiently through early development to speed up decision making and progression to later-stage trials.

Company size
1,001-5,000
Company stage
Early VC
Total funding
$6.7M
Headquarters
Laval, Canada
Founded
1976

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