Phlebotomist/Laboratory Assistant [Bilingual]

About Us

At Rovia Clinical Research, we’re shaping the future of community clinical research by being the partner of choice for CROs, Sponsors, and PIs. Our team of skilled professionals includes talented and driven individuals from all backgrounds.

People First – Humility – Integrity – One Team – Results Accountability

Position Summary

The Phlebotomist/Laboratory Assistant assists with the execution of new studies and the maintenance of open and closed studies, performing administrative and clinical tasks for trials. This position works in close collaboration with Clinical Research Coordinators, Research Assistants, sponsors, and compliance to carry out responsibilities per the study protocol.

Duties/Responsibilities

• Performs phlebotomy, using appropriate collection techniques to obtain quality samples from all age groups and patient populations.
• Collects, labels, and processes research samples according to study protocols and Rovia SOPs.
• Performs various laboratory tests and assays, including biochemical, hematological, and molecular analyses.
• Analyzes laboratory data, interprets results, and prepares reports for review by the research staff.
• Assists the Principal Investigator (PI) and other research staff to ensure clinical research and related activities are performed in accordance with federal regulation and Rovia SOPs.
• Maintains inventory of laboratory supplies and reagents, ordering supplies as needed and ensuring proper storage and handling of materials.
• Develops a working familiar with study protocol, including study procedures and timelines, inclusion and exclusion criteria, confidentiality, and privacy protections.
• Records and maintains accurate documentation of laboratory procedures, test results, and other relevant information in accordance with regulatory requirements.
• May perform other job-related duties as requested or required.
  
  

Required Skills/Abilities

• Sound knowledge of medical terminology.
• Sound knowledge of ICH/GCP and Regulatory requirements.
• Knowledge of Good Clinical Practice (GCP) and FDA and HIPAA policies and practices.
• Excellent interpersonal skills to work effectively with colleagues, clinicians, patients, administrators, auxiliary personnel, regulators, monitors and sponsors.
• Strong organizational skills.
• Proficient in the use of Microsoft Office and Excel.
• Fluent in spoken and written English and Spanish.
• Meticulous attention to detail.
• Ability to maintain confidentiality.
  
  

Education And Experience

• High school diploma required.
• Phlebotomy experience and/or certification required.
• Experience in a laboratory setting required, preferably in a clinical research environment.
• Familiarity with laboratory equipment and instrumentation (centrifuges, spectrophotometers, PCR machines, etc.) required.
• Current GCP and IATA certification preferred or must be obtained upon hire.
  
  

The Pay Range For This Role Is

20 - 22 USD per hour(IMIC)