Laboratory Coordinator / Phlebotomist

Alcanza Clinical Research

Maitland, FLOn-siteFull time
Invite-only right now: save jobs, track applications, build tailored resumesAlready have an account? Log in
Location
Maitland, FL
Work style
On-site
Job type
Full time
Posted
Oct 8
11 days ago
Career path

See where this role leads

Jigup maps the next three moves from a job like this one, with the titles and the skills each step asks for.

Join the waitlist

About the company

Alcanza Clinical Research

Research · 201 to 500 employees

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.

Alcanza Clinical Research on LinkedIn

What you'll do

  • 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.

What you need

  • 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.
  • Education: a high school diploma or an associate degree

Key skills

clinical laboratory processingMicrosoft applicationselectronic health records40+ wpmStrong organizational skillsattention to detailinterpersonal and listening skillsHIPAA guidelines

Keywords for your resumePro

The words this employer's screening is likely to look for.

This job lists resume keywords

The terms this posting uses, pulled out so you can mirror them in your resume. Jigup Pro members see the list on the job board.

Join the waitlist

Perks

  • Medical
  • dental
  • vision
  • life insurance
  • short and long-term disability insurance
  • health savings accounts
  • supplemental insurances

See full description on company page, apply now

Read the full posting here
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 ResponsibilitiesEssential Job Duties: Responsibilities may include but are not limited to:Draw and process specimens according to each trial’s requirementsAssist with specimen shipments to central labs and ensure proper shipping methods have been observedMonitor expiration dates on lab equipment and supplies Unpack and put away incoming lab supply shipmentsMonitor and maintain both general and study-specific lab inventory, and ensure study-specific lab supplies are ready for new study start-upTransport samplesProvide 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 guidelinesMaintaining confidentiality of patients, customers, and company information, andPerforming other related activities as assigned.Skills, Knowledge and ExpertiseMinimum 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.BenefitsFull-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.

More entry level jobs in Maitland, FL

All jobs in Florida

More jobs at Alcanza Clinical Research

Ready to apply?

Jigup is invite-only right now. Join the waitlist to save jobs, track applications, and build tailored resumes.

Join the waitlist