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Alcanza Clinical Research logo

Lab Coordinator

Alcanza Clinical Research·Woodstock, New York

Full Time·On Site·0-2 yrs·Posted 7 days ago
Practice for this role

About the role

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 ensure all lab equipment is maintained and up to date.

Lab Coordinator Department

  • Operations
  • Employment
  • Type:
  • Full
  • Time
  • Location: North Georgia Clinical Research - Woodstock, GA

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 Essential Job Duties: Responsibilities may include but are not limited to:

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.

Requirements

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.

  • high school
  • associate degree
  • Attention To Detail
  • Interpersonal Skills
  • Written Communication
  • Verbal Communication
  • Inventory Management
  • Time Management
  • Organizational Skills
  • Confidentiality
  • Phlebotomy
  • Electronic Health Records
  • HIPAA Regulations
  • Microsoft Office
  • Specimen Processing
  • ICH Guidelines
  • GCP Compliance
  • IATA Training

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
0-2 yrs
Location
Woodstock, New York
Posted
Jul 21, 2026
Application
Employer website
Alcanza Clinical Research logo

Hiring organization

Alcanza Clinical Research

At Alcanza℠, we believe in the power of clinical research to move healthcare forward for all patients. Because research is the first step in bringing approved treatments to market, we encourage everyone to learn more about participating.

IndustryResearch Services
TypePrivately Held
Size201-500 employees
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Market context

Lab coordinator roles in New York

Lab coordinator openings in New York are often tied to busy clinical and hospital lab settings, where steady processing work and accurate coordination are essential. These roles can be competitive because employers look for candidates who combine lab processing experience with strong computer, organization, and communication skills. Review the AI-summarized requirements and benefits here to save research time, and tailor your application to highlight hands-on processing experience and software proficiency.

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