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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Phase 1 Research Phlebotomist/Data Entry (AMP) - **Company:** Arizona Liver Health - **Location:** Chandler, AZ, United States - **Experience:** Starter - **Salary:** $47,840.0 - $54,080.0 - **Contract:** Permanent contract - **Skills:** Clinical Trial Management Systems, Databases, Graphical Data Display Manager, Data Import/Export, Electronic Medical Records - **Published:** October 28, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=fcec00a0b26540a7 ## About the Role * High School Diploma or GED required * Associate Degree or Bachelors degree preferred * Professional certification in phlebotomy from a recognized program * At least 1 year of clinical research experience as a clinical research coordinator and experience working in a medical center or private practice is strongly preferred * Experience using CTMS system and EDC program Knowledge, Skills, Abilities: * Excellent communication and problem-solving skills * Advanced written and verbal communication skills * Ability to work effectively with a lead study coordinator on multiple assignments, in a fast paced, multi-tasked environment, exercising sound judgment in setting priorities with a strong attention to detail * Bilingual - Spanish preferred * Demonstrated ability to multi-task. * Demonstrated excellent organizational skills. * Ability to communicate effectively both orally and in writing. * Demonstrated experience working as part of a team. * Relevant subject matter knowledge. * Ability to successfully draw blood from patients with minimal or no complications * Empathy and interpersonal skills for working with patients * Detail-oriented and committed to ensuring patient confidentiality * Data entry and computer skills * Strong attention to detail * A thorough understanding of clinical research requirements, principles of GCP, and biomedical research ethics. * Interpersonal and communication skills-interact effectively with professional and administrative staff, sponsor, regulatory representatives, patients, potential subjects and referral sources. * Ability to provide all employees and research subjects with an excellent service experience by consistently demonstrating professional decorum. ## Description Reasonable accommodation may be made to enable individuals with disabilities to perform these essential functions. Data Entry: * File documents in the binder (I.e., subject source, labs) * Enter clinical research data into appropriate fields. * Transfer data from paper formats via computer, recorders, or scanners * EDC entry * Review and edit data to ensure completeness and accuracy of information; follow up with subjects to resolve problems or clarify data collected. * Answer Queries * Serve as back up for pharmacy and lab * Curate data directly from clinical research * Analyze statistical and graphical Data. * Conduct clinical research study visits when assigned. * Audit research trials * Prepare documents and charts for subject visits. * Assist patients with surveys * Perform vital signs, arthrometric measurements, transient elastography, and EKG's * Quality control research visits and informed consent before screening visit is over * Confirm correct IP prior to dispensation * File the signed copy in the subject binder * Obtain and print procedural/imaging reports for review by the investigator * Print labs and prepare for Investigator to review * File lab results to subject binder or where required * Ensure W-9 and medical release forms are signed by subjects annually * Conduct clinical research study visits when assigned * Audit research trials * Prepare correspondence, documentation, or presentation materials on findings * Assist with the management of study supplies and order resupply * Perform miscellaneous job-related duties as assigned * Request medical records prior to visit and print for filing as needed * Plan, schedule, and confirm of subject research visits as needed * Update CTMS as needed * Maintain training as needed including but not limited to GCP, IATA, EDC, Protocol training, * Delegation of Authority and others as required Phlebotomy: * Ensure adherence to protocol during study conduct and performing specific administrative and clinical procedures * Prepare patients before drawing blood * Explain blood draw procedures to patients and answering any questions about the process * Follow all health and safety protocols and procedures to maintain sanitary work areas * Gathering medical testing materials, including needles, sample vials, blood storage bags and test tubes * Verify patient information and labeling blood samples properly * Obtain blood specimens from patients per laboratory orders by performing venipunctures and finger sticks, process medical laboratory tests and document results * Update patient information in the organization's database * Help nervous or frightened patients remain calm during blood draws * Review the laboratory schedule and verify and complete orders. Identify the patient and confirm the correct patient record. Monitor and resolve orders in the electronic medical record and/ or subject source for clinical research * Complete appropriate laboratory forms documenting tests performed and providing diagnoses correlating to tests performed * Complete lab requisition forms and produce appropriate labels for forms and specimen tube * Enter patient demographics, tests performed, or other required information on the lab requisitions * Keep an inventory, order and maintain adequate laboratory supplies * Clean and maintain the laboratory including equipment * Maintain records and documentation for proficiency testing and to meet COLA and CLIA requirements and regulations * Serve as a back-up for clinical team members as needed by controlling patient flow, performing EKG tests, obtaining blood pressure measurements, documenting vital sign * Work with Providers and Clinical Research Coordinators and following their directions * Answer research queries as designated by CRC's