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Clinical Laboratory Specialist

2 months ago


San Leandro, California, United States Fellow Full time

About Fellow

At Fellow, our mission is to enhance male fertility support accessibility for all individuals, regardless of their circumstances. We strive to address the critical questions surrounding male reproductive health and empower clinicians through our research initiatives. Our goal is to establish a leading male reproductive sciences organization that significantly improves patient-clinician interactions that have historically faced challenges.

About this Role

The Clinical Laboratory Scientist (CLS) is essential to the functioning of our Clinical Laboratory. The CLS is tasked with executing complex laboratory tests on patient samples, ensuring quality control and assurance, reporting results accurately, and adhering to all relevant local, state, and federal laboratory regulations.

This role requires excellent verbal and written communication abilities, the capability to juggle multiple responsibilities concurrently, and the flexibility to adapt to various tasks and schedules. Additionally, the CLS must demonstrate the ability to work independently while contributing to a collaborative team environment.

This is a part-time position for a six-month contract, with the potential for transition to a full-time, permanent role. The schedule consists of 28 hours per week, from Tuesday to Friday, 9:30 AM to 5:00 PM.

Key Responsibilities

  • Conduct laboratory tests and analyses in accordance with established standard operating procedures.
  • Analyze, interpret, and document patient results in the Laboratory Information Management System (LIMS).
  • Oversee unlicensed personnel during the pre-analytical, analytical, and post-analytical phases.
  • Independently identify and resolve complex issues that may impact test outcomes.
  • Perform routine maintenance on laboratory equipment as per standard operating procedures.
  • Execute, review, and document quality control processes within the laboratory.
  • Record all corrective actions taken when laboratory performance deviates from established specifications.
  • Identify opportunities for process enhancement and communicate them to laboratory management.
  • Assist in training new laboratory staff.
  • Support internal audits and preparation for inspections as required.
  • Maintain adequate inventory of laboratory supplies and prepare necessary reagents for testing.
  • Conduct and document reagent qualification following approved protocols.
  • Draft and revise standard operating procedures.
  • Carry out additional laboratory duties as assigned and assist colleagues as time permits.
  • Engage in projects, provide updates on progress, and fulfill assignments.
  • Report any concerns regarding test quality or safety to the appropriate supervisory personnel.

Qualifications

  • Valid Clinical Laboratory Scientist license in California.
  • Bachelor's degree in Biomedical Laboratory Science, Clinical Science, or a related discipline.
  • Experience in a high-complexity clinical laboratory environment is preferred.
  • Familiarity with local, state, and federal laboratory regulations.
  • Strong knowledge of laboratory safety protocols and the ability to handle potentially hazardous materials.
  • Proficient in laboratory information systems (LIS), Microsoft Office Suite, and Google applications.
  • Exceptional organizational skills and attention to detail.
  • Ability to work autonomously and collaboratively in a fast-paced setting.
  • Strong communication skills, both verbal and written, adhering to best documentation practices.
  • Capable of executing tasks independently with minimal guidance while maintaining a collaborative spirit.
  • Ability to prioritize tasks with a focus on quality and timeliness.
  • Proactively initiate and drive projects, consistently contributing innovative solutions and identifying process improvement opportunities.
  • Willingness to participate in projects, provide updates, and complete assignments as expected.

Work Environment

  • Work hours and days may vary based on operational requirements.
  • Prolonged standing or sitting may be necessary.
  • Exposure to hazardous materials, biological specimens, and laboratory equipment may occur.
  • Repetitive manual pipetting may be required.

Why You'll Appreciate Working Here

We foster a culture of empathy and community, driven by excellence, that not only helps you achieve your goals but also encourages you to set new ones. We value individual expression in the workplace and thrive on the innovative ideas that arise from it. Your contributions will play a vital role in transforming an industry that is ready for change.

Fellow is an equal opportunity employer. We prohibit discrimination and harassment of any kind and provide equal employment opportunities to all employees and applicants, regardless of race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. We value diversity and the unique perspectives that each individual brings to our workforce.