Alcanza Clinical Research
Location
Sugar Land, Texas
The Lab Coordinator is responsible for drawing and processing specimens in compliance with GCP, ICH, and HIPAA regulations. They also manage lab inventory, handle specimen shipments, and support clinical research activities such as recruitment and QA review.
A high school diploma and at least one year of clinical laboratory processing experience are required, while an associate degree is preferred. Candidates must be proficient in computer applications and possess strong organizational and communication skills.
Description Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Lab Coordinator works to ensure the execution of assigned lab procedures in compliance with GCP, ICH, FED and HIPAA regulations, company SOPs, and policies.
Key Responsibilities Essential Job Duties: Responsibilities may include but are not limited to:
Skills, Knowledge and Expertise
High School diploma or equivalent and a minimum of 1 year of clinical laboratory processing experience is required. Associates degree is preferred. Bilingual (English/Spanish) skills are a plus.
Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
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