Laboratory Coordinator / Phlebotomist
Alcanza Clinical Research
- Location
- Maitland, FL
- Work style
- On-site
- Job type
- Full time
- Posted
- Oct 8
- 11 days ago
Career path
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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.
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
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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