Lab Coordinator / Phlebotomist

Benefits

Qualifications

• •Minimum Qualifications: High School diploma or equivalent and a minimum of 1 year of clinical laboratory processing experience is required
• •Blood draw experience is required
• •Proficiency with computer applications such as Microsoft applications, email, electronic health records, and web applications, and the 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
• •7 more items(s)

Responsibilities

• •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
• •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, and
• •Performing other related activities as assigned
• •11 more items(s)