Laboratory Tech I / II
CenExel
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 judgement are required to perform analytical processes.
Job description
Essential Responsibilities and Duties
- Must be able to effectively communicate verbally and in writing in both English and Spanish.
- 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.
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
- Indoor, Clinic environment.
- Essential physical requirements include sitting, typing, standing, and walking.
- Lightly active position, occasional lifting of up to 20 pounds.
- Reporting to work, as scheduled, is essential.
- This is an on-site work arrangement.
Requirements
- Must be able to effectively communicate verbally and in writing in both English and Spanish.
- Minimum High School graduate or have GED equivalency.
- Have full knowledge of laboratory procedures and processes per protocol, laboratory manual, shipping manual, etc.
- IATA certification, preferred.
- Phlebotomist certification preferred.
- Motivated to work consistently in a fast-paced and rapidly changing environment.
Benefits
- Health Insurance
- Dental
- Vision
- LTD
- STD
- Life Insurance
- 401(k)
Company overview
CenExel is a leading integrated clinical research site network operating across major metropolitan areas throughout the United States. Founded in 2018 and headquartered in Salt Lake City, Utah, the company operates 18 Centers of Excellence that collectively represent over 40 years of clinical research experience. CenExel specializes in providing comprehensive clinical trial services to pharmaceutical companies, biotechnology firms, and clinical research organizations, with particular expertise in central nervous system (CNS) disorders and early-phase clinical research. The company's nationwide network delivers deep scientific expertise, premium data quality, operational efficiencies, and exceptional patient engagement to drive successful clinical trial outcomes. With more than 1,200 employees across its network, CenExel focuses on accelerating the development of life-changing therapies through its patient-centered approach and commitment to research excellence. The company serves as a strategic partner for sponsors seeking to optimize clinical trial performance, from site selection through study close-out, while maintaining rigorous standards for patient care and scientific integrity.