Laboratory Technician, PRN

CenExel

Posted 2 months ago

Full Time

Evesham Township, New Jersey

In Person

Smart Summary

Responsibilities

The laboratory technician performs diagnostic testing and manages laboratory activities including sample collection, processing, and storage. They ensure adherence to clinical protocols, FDA regulations, and GCP standards while maintaining accurate laboratory logs and inventory.

Qualifications

You have a High School graduate or GED equivalency and possess the ability to communicate effectively both verbally and in writing. You are motivated to work in a fast-paced environment and may possess preferred certifications such as IATA or Phlebotomist.

Must Have Skills for ATS

IATA certification

Phlebotomist certification

Job Description

About Us:

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Job Summary:

Performs select diagnostic testing and basic activities necessary to provide laboratory testing services. Testing scope may cross several laboratory disciplines such as hematology, urinalysis, and/or chemistry. Minimal interpretation and judgment are required to perform analytical processes.

Schedule: Monday - Friday mornings and weekends as needed. 

Compensation: $19.00 - 23.00/hr. (Depending on education, experience, and skillset)

Essential Responsibilities and Duties:

  • Have full knowledge of laboratory procedures and processes per protocol, laboratory manual, shipping manual, etc.
  • Assist the laboratory manager in site preparation for study conduct.
  • Assist in the creation of laboratory documents (i.e. harvest logs, etc.)
  • Assist in the preparation of collection tubes, vials, study supplies for visits.
  • Monitor temperature of laboratory sample storage and address any excursions.
  • Maintain harvest logs, chain of custody, laboratory sample manifest/inventory logs and/or memos.
  • Pack and properly label all study materials for storage or return to sponsor upon study close out.
  • Obtains samples per protocol, performs select diagnostic tests or limited high complexity testing and documents process in source documents.
  • Assists in gathering data for validations on select instrumentation.
  • Assists with monitoring supply inventory.
  • Stores samples in an upright position in appropriate shipping boxes in the freezer.  Stores primary and secondary samples in separate shipping boxes.
  • Ensures freezer/refrigerator temperature is within range for protocol and ensures appropriate logs are kept.
  • Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

  • Must be able to effectively communicate verbally and in writing.
  • Minimum High School graduate or have GED equivalency.
  • IATA certification, preferred.
  • Phlebotomist certification preferred.
  • Motivated to work consistently in a fast-paced and rapidly changing environment.

Working Conditions

  1. Indoor, Clinic environment.
  2. Essential physical requirements include sitting, typing, standing, and walking.
  3. Lightly active position, occasional lifting of up to 20 pounds.
  4. Reporting to work, as scheduled, is essential.
  5. This is an on-site work arrangement.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

CenExel

CenExel is a leading integrated, wholly owned, nationwide clinical research site network comprised of 18 Centers of Excellence in major metropolitan areas across the U. S. With 40+ years of experience, our Centers of Excellence deliver deep scientific expertise, premium data, operational efficiencies, and exceptional patient engagement to drive successful complex clinical trial outcomes. The world's most results-driven Pharma, Biotech, and Clinical Research Organizations trust our strategic approach and benefit from our collaboration and unified sites’ commitment to real world solutions. Rely on us to confidently progress from site selection to study close-out and accelerate life-changing therapies. Get more value from your clinical trials with CenExel.
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