Lab Coordinator / Phlebotomist

Alcanza Clinical Research•Lakeland, FL

8h•Onsite

About The Position

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.

Requirements

High School diploma or equivalent
Minimum of 1 year of clinical laboratory processing experience
Blood draw experience
Proficiency with computer applications such as Microsoft applications, email, electronic health records, and web applications
Ability to type proficiently (40+ wpm)
Strong organizational skills and attention to detail
Well-developed written and verbal communication skills
Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers
Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities
Must be professional, respectful of others, self-motivated, and have a strong work ethic
Must possess a high degree of integrity and dependability
Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines

Nice To Haves

Associates degree is preferred
Bilingual (English/Spanish) skills are a plus

Responsibilities

Draw and process specimens according to each trial’s requirements
Assist with specimen shipments to central labs and ensure proper shipping methods have been observed
Monitor expiration dates on lab equipment and supplies
Unpack and put away incoming lab supply shipments
Monitor and maintain both general and study-specific lab inventory, and ensure study-specific lab supplies are ready for new study start-up
Transport samples
Provide mentoring to new hires and allow them to shadow you as they learn.
Complete and renew CITI GCP and IATA training as required.
Attend SIVs when needed, and complete all sponsor-required lab training.
May support other clinical research-related activities such as recruitment, EDC and QA/Chart review as needed.
Ensuring compliance with company SOPs, FDA/HIPAA regulations, ICF documentation, and GCP guidelines
Maintaining confidentiality of patients, customers, and company information
Performing other related activities as assigned.