Laboratory Tech II / Specimen Processor at CenExel

Evesham Township, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Sep, 26

Salary

24.9

Posted On

14 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Diagnostic Testing, Specimen Processing, Laboratory Procedures, Sample Management, IATA Certification, Phlebotomy, FDA Regulations, ICH Guidelines, GCP, Inventory Monitoring, Data Documentation, Clinical Trial Support

Industry

Research Services

Description

CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Job Summary: Responsible for conducting basic to moderately complex diagnostic testing. Performs basic interpretation and limited problem resolution with guidance from senior lab techs, as needed. Compensation: $20.21 - $24.90 /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. • Assists the laboratory manager in site preparation for study conduct. • Assists in the creation of laboratory documents (harvest logs, etc.) • Assists in the preparation of collection tubes, vials, study supplies for visits. • Monitors temperature of laboratory sample storage and address any excursions. • Maintains harvest logs, chain of custody, laboratory sample manifest/inventory logs and/or memos. • Packs and properly labels all study materials for storage or return to sponsor upon study close out. • Obtains samples per protocol, performs select diagnostic test 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 have proper experience and demonstrate mastery of Lab Technician I position. • 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. • Must be able to effectively communicate verbally and in writing. 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.

Responsibilities

Responsible for conducting basic to moderately complex diagnostic testing and specimen processing within a clinical research environment. Duties include maintaining harvest logs, monitoring storage temperatures, and ensuring strict adherence to FDA and GCP guidelines.