Alcanza Clinical Research

Inclusive clinical trials for diverse patients

Laboratory Coordinator / Phlebotomist

Diagnostics & Laboratory ProfessionalsUpdated on Nov 13

Full-timeMaitland, FL, USANo salary listed

About the Job

Requirements

A high school diploma or equivalent and at least one year of clinical laboratory processing experience are required.
Proficiency with Microsoft applications, email, electronic health records, and web applications, and the ability to type at least 40 words per minute.
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 independently and with coworkers, subjects, managers, and external customers.
Ability to handle multiple tasks effectively and adapt to changes in workloads and priorities.
Professionalism, respect for others, self-motivation, and a strong work ethic.
High integrity and dependability.
Ability to handle highly sensitive information confidentially and professionally, in compliance with HIPAA guidelines.

Responsibilities

Draw and process specimens according to each trial’s requirements.
Assist with specimen shipments to central labs and ensure proper shipping methods are followed.
Monitor expiration dates on lab equipment and supplies.
Unpack and put away incoming lab supply shipments.
Monitor and maintain 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 while they learn.
Complete and renew CITI GCP and IATA training as required.
Attend SIVs when needed and complete sponsor-required lab training.
Support other clinical research-related activities, such as recruitment, EDC, and QA/chart review, as needed.
Ensure compliance with company SOPs, FDA/HIPAA regulations, ICF documentation, and GCP guidelines.
Maintain confidentiality of patient, customer, and company information.
Perform other related activities as assigned.

Desired Qualifications

An associate degree is preferred.
Bilingual English/Spanish skills are a plus.

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.

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.

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.

About the Company

Alcanza Clinical Research

Inclusive clinical trials for diverse patients

Alcanza Clinical Research conducts inclusive clinical trials by partnering with pharmaceutical companies, medical providers, and community organizations to enroll diverse patient populations across major therapeutic areas. Its studies follow established protocols with certified research professionals to ensure patient safety and data integrity, while participants may receive health tests and access to emerging treatments at no cost. The company differentiates itself through active community collaboration, broad patient diversity, and education alongside trial execution, expanding trial reach. Its goal is to speed the development of new therapies by removing participation barriers and delivering high-quality, diverse clinical research.

Company size: 201-500
Company stage: Not listed
Total funding: Not listed
Headquarters: Lake Mary, FL
Founded: 2021

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