Clinical Lab Supervisor

Kelly
Port Chester, NY Full Time
POSTED ON 10/26/2022 CLOSED ON 10/31/2022

What are the responsibilities and job description for the Clinical Lab Supervisor position at Kelly?

Kelly Science and Clinical is searching for a Temp-To-Hire Clinical Supervisor in Port Chester, ny.


The Clinical Supervisor will be responsible for operational accountability, development and implementation of strategies and corporate polices surrounding the design and execution of clinical research studies for safety and claims. The managing and reporting of the clinical studies will be in accordance with the company’s SOP’s and under the guidelines of Good Clinical Practices (GCP).


The Clinical Supervisor has the following duties:

  • Participates and coordinates the planning, development and implementation of clinical protocols, logistical procedures and operating systems in accordance with parameters set out by the study sponsor and Principal Investigator.
  • Supervises, evaluates and coordinates the activities of a team of Clinical Study Coordinators and Clinical Technicians; ensures that all clinical activities are carried out in accordance with Company SOP's and guidelines of Good Clinical Practices.
  • Ensures that all the research activities are conducted in compliance with any pertinent regulatory requirements, and with the highest standards of scientific/clinical expertise.
  • Creates and monitors clearly defined quality methods for staff to apply. Defines quality procedures in conjunction with operating staff.
  • Oversee QA/QC operation of the department to ensure compliance to regulations and processes.
  • Works closely with Clinical Management to ensure staff is adequately trained and that documentation is in place on clinical practices including bioinstrumentation and other clinical safety and efficacy procedures.
  • Other duties as may be required.

Position Requirements:

  • Minimum Bachelor’s degree in life sciences.
  • 2 years’ experience of Clinical Industry experience
  • Clinical trial development, including regulatory aspects of clinical trials.
  • Knowledge of Good Clinical Practices (GCP) and Good Document Practices (GDP).
  • Experience with supervising/managing subordinates.


You should know:
Your safety matters! Vaccination against COVID-19 may be a requirement for this job in compliance with current client and governmental policies. A Kelly recruiter will confirm and share more details with you during the interview process.

Why Kelly®?

Kelly® Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.

About Kelly®

At Kelly, we’re always thinking about what’s next and advising job seekers on new ways of working to reach their full potential. In fact, we’re a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.

Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law.

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