Lab Coordinator / Phlebotomist

Accel Research Sites; North Charleston (SC); On-site; USD 40,000 - 60,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k plan with safe harbor match

Life insurance

Job summary

Alcanza is a growing multi-site clinical research company seeking a Lab Coordinator / Phlebotomist to support operations at Coastal Carolina Research Center in Charleston, SC.

The role ensures laboratory procedures comply with GCP, ICH, FED and HIPAA regulations, and SOPs. Responsibilities range from specimen handling to training, shipments, inventory and QA.

Qualifications

• High School diploma or equivalent required; 1 year of clinical lab processing experience preferred.
• Associates degree preferred.
• Bilingual English/Spanish a plus.

Responsibilities

• Draw and process specimens per trial requirements.
• Assist with specimen shipments to central labs and ensure proper shipping methods.
• Monitor expiration dates on lab equipment and supplies.
• Unpack and store incoming lab shipments.
• Maintain study-specific lab inventory and prep supplies for new studies.
• Transport samples between locations as needed.
• Mentor new hires and supervise shadowing sessions.

Skills

Proficiency with computer applications

Strong organizational skills

Written and verbal communication

Interpersonal and listening skills

Multitasking and adaptability

Integrity and dependability

HIPAA compliance

Education

High School diploma or equivalent

Associates degree preferred

Job description

Lab Coordinator / Phlebotomist

Department: Operations

Employment Type: Full Time

Location: Coastal Carolina Research Center | Charleston, SC

Reporting To: Susan English

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, VA, SC, TN, TX 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

• 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.

Skills, Knowledge and Expertise

Minimum Qualifications: 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.

Required Skills:

• 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.

Benefits

• 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.