Phase 1 Research Phlebotomist/Data Entry (AMP)

Arizona Liver Health • Chandler, AZ

7d • $23 - $26

About The Position

Arizona Liver Health/Arizona Clinical Trials is seeking a Research Phlebotomist/Data Entry professional for its Chandler location. The role supports clinical research operations through accurate data entry, study visit preparation and conduct, trial auditing, patient support, and phlebotomy and laboratory procedures. It also helps maintain study documentation, supplies, records, and regulatory compliance, and may provide backup support to pharmacy and clinical team members. Some interoffice travel may be required using a company vehicle or with mileage reimbursement.

The position is full-time, scheduled Monday through Friday from 7:00 a.m. to 4:00 p.m. Compensation is $23–$26 per hour, depending on experience. Arizona Liver Health describes its mission as advancing medical innovation and high standards of care through clinical trials, with a focus on patient safety, regulatory compliance, and high-quality clinical data.

Requirements

• High school diploma or GED.
• Professional certification in phlebotomy from a recognized program.
• Ability to successfully draw blood from patients with minimal or no complications.
• Data-entry and computer skills, including experience using a CTMS system and an EDC program.
• Strong communication, problem-solving, organizational, and interpersonal skills, with the ability to communicate effectively orally and in writing.
• Ability to multitask and work effectively with a lead study coordinator on multiple assignments in a fast-paced environment, using sound judgment to set priorities and maintaining close attention to detail.
• Ability to work as part of a team and interact effectively with professional and administrative staff, sponsors, regulatory representatives, patients, potential subjects, and referral sources.
• Thorough understanding of clinical research requirements, GCP principles, and biomedical research ethics.
• Empathy and interpersonal skills for working with patients, commitment to patient confidentiality, and ability to provide professional service to employees and research subjects.
• Some interoffice travel may be required; travel may use a company vehicle or mileage reimbursement.

Nice To Haves

• Associate or bachelor's degree.
• At least one year of clinical research experience as a clinical research coordinator, as well as experience working in a medical center or private practice.
• Bilingual Spanish.

Responsibilities

• File subject source documents, laboratory results, and other documents in the appropriate binders.
• Enter clinical research data into appropriate fields, including EDC systems, and transfer information from paper formats using computers, recorders, or scanners.
• Review and edit data for completeness and accuracy, follow up to clarify data or resolve problems, and answer research queries.
• Curate data from clinical research and analyze statistical and graphical data.
• Conduct assigned clinical research study visits and audit research trials.
• Prepare documents and charts for subject visits, assist patients with surveys, and obtain and print medical records, procedural reports, imaging reports, and laboratory results for investigator review and filing.
• Perform vital signs, anthropometric measurements, transient elastography, and EKGs; quality-check research visits and informed consent before the screening visit is completed.
• Confirm the correct investigational product before dispensation and file signed copies in the subject binder.
• Ensure subjects sign W-9 and medical release forms annually.
• Prepare correspondence, documentation, or presentation materials regarding findings.
• Assist with study-supply management and order resupplies.
• Plan, schedule, and confirm subject research visits as needed, and update the CTMS.
• Maintain required training, including GCP, IATA, EDC, protocol, and Delegation of Authority training.
• Follow study protocols and perform required administrative and clinical procedures.
• Prepare patients for blood draws, explain procedures, answer questions, and help nervous patients remain calm.
• Gather phlebotomy materials; verify patient information; label samples; and obtain blood specimens through venipuncture and finger sticks.
• Process medical laboratory tests, document results, update patient information, and complete laboratory and requisition forms and specimen labels.
• Review laboratory schedules, verify and complete orders, identify patients and confirm records, and monitor and resolve orders in the electronic medical record or research subject source.
• Follow health and safety protocols, maintain sanitary work areas, clean and maintain laboratory equipment, and keep adequate laboratory supplies through inventory and ordering.
• Maintain proficiency-testing records and documentation to meet COLA and CLIA requirements and regulations.
• Back up clinical team members by helping manage patient flow, performing EKGs, measuring blood pressure, and documenting vital signs.
• Work with providers and Clinical Research Coordinators under their direction.
• Perform other job-related duties as assigned.

Benefits

• Health, dental, and vision coverage, including HSA plans with an employer contribution.
• Two weeks of PTO.
• Five days of sick time.
• Seven company holidays and two half-days.
• 401(k) with company match.
• Short- and long-term disability.
• Educational assistance.
• Shared company vehicles for required travel.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED