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Entry Level Phlebotomy Jobs in Georgetown, TX (NOW HIRING)

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Entry Level Phlebotomy information

See Georgetown, TX salary details

$12

$18

$26

How much do entry level phlebotomy jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for entry level phlebotomy in Georgetown, TX is $18.79, according to ZipRecruiter salary data. Most workers in this role earn between $16.06 and $21.20 per hour, depending on experience, location, and employer.

What is entry level phlebotomy?

Entry-level phlebotomy refers to the starting position for individuals who collect blood samples from patients for medical testing, transfusions, or donations. Entry-level phlebotomists typically work in hospitals, clinics, laboratories, or blood donation centers under the supervision of more experienced staff. They are responsible for preparing patients, using proper techniques to draw blood, labeling samples accurately, and ensuring patient comfort and safety. Most entry-level positions require completion of a phlebotomy training program and certification, but extensive prior experience is not necessary.

What are the key skills and qualifications needed to thrive as an entry level phlebotomist?

To thrive as an Entry Level Phlebotomist, you need a basic understanding of venipuncture, specimen collection, and infection control, usually supported by a high school diploma and a phlebotomy certification. Familiarity with laboratory information systems (LIS), blood collection equipment, and safety protocols is essential. Attention to detail, steady hands, and strong interpersonal skills help you interact professionally with patients and accurately collect samples. These skills are vital for ensuring patient comfort, preventing errors, and maintaining the integrity of laboratory results.

What are some common challenges faced by entry level phlebotomists, and how can they be overcome?

Entry-level phlebotomists often face challenges such as working with patients who have difficult veins, managing nervous or anxious individuals, and maintaining accuracy in labeling and handling specimens. Building strong communication skills, practicing proper technique, and seeking mentorship from experienced colleagues can help overcome these obstacles. Additionally, adhering to strict safety and hygiene protocols is essential to ensure patient safety and minimize errors. Over time, increased exposure and hands-on practice will boost confidence and proficiency in the role.

What is the difference between Entry Level Phlebotomy vs Medical Assistant?

AspectEntry Level PhlebotomyMedical Assistant
CertificationsPhlebotomy Technician CertificationCPR, Medical Assistant Certification (optional)
Work EnvironmentHospitals, clinics, blood donation centersDoctor's offices, clinics, hospitals
Job DutiesDrawing blood, specimen collectionPatient intake, basic clinical tasks, administrative duties

Entry Level Phlebotomy focuses primarily on blood collection and specimen handling, often in clinical or blood bank settings. Medical Assistants perform a broader range of clinical and administrative tasks. While both roles may work in healthcare environments, their certifications, responsibilities, and daily duties differ significantly.

How to get your first job as an entry level phlebotomy?

To secure an entry-level phlebotomy position, obtain a high school diploma or equivalent, complete a certified phlebotomy training program, and earn a phlebotomy certification from an accredited organization. Gaining hands-on experience through internships or externships can improve job prospects, and applying to healthcare facilities or laboratories is the next step.

Is it hard to get a job as a new entry level phlebotomy?

Entry level phlebotomy positions are generally accessible to those with a certification and basic training, making it possible for new entrants to find employment. Competition can vary by location, but having certification, good communication skills, and a clean background can improve job prospects.

When to start applying for entry level phlebotomy jobs?

Entry level phlebotomy jobs can typically be applied for once you have completed a phlebotomy training program and obtained any required certification, which often takes a few months. It is advisable to start applying soon after certification to gain experience and secure a position in a healthcare setting.

What are the most commonly searched types of Phlebotomy jobs in Georgetown, TX?

The most popular types of Phlebotomy jobs in Georgetown, TX are:

What are popular job titles related to Entry Level Phlebotomy jobs in Georgetown, TX?

For Entry Level Phlebotomy jobs in Georgetown, TX, the most frequently searched job titles are:

What job categories do people searching Entry Level Phlebotomy jobs in Georgetown, TX look for?

The top searched job categories for Entry Level Phlebotomy jobs in Georgetown, TX are:

What cities near Georgetown, TX are hiring for Entry Level Phlebotomy jobs?

Cities near Georgetown, TX with the most Entry Level Phlebotomy job openings:

Entry Level Phlebotomy jobs near you
Infographic showing various Entry Level Phlebotomy job openings in Georgetown, TX as of August 2026, with employment types broken down into 3% As Needed, 77% Full Time, 14% Part Time, and 6% Contract. Highlights an 88% Physical, and 12% Remote job distribution, with an average salary of $39,074 per year, or $18.8 per hour.

Clinical Research Coordinator I

Austin, TX • On-site

Texas Diabetes & Endocrinology, P.A.
Health Care and Social Assistance • 51 - 200 employees
Learn more about Texas Diabetes & Endocrinology, P.A.external

$60 - $80/hr

Other

Posted 2 days ago

New

Job description

Job DetailsJob Location: Central Office (Mopac/Far West) - Central Austin, TX 78731

Texas Diabetes and Endocrinology PA (TD&E) has grown over the years to meet the Endocrinology needs of the Austin community. Our mission is to strive to provide expert care in Diabetes Thyroid problems Osteoporosis Weight management and hormonal conditions by providing thorough evaluations and innovative personalized solutions focused on our patients success. Our employees are the strength that keeps us moving forward.

Our Clinical Research Department is looking for a Clinical Research Coordinator CRC I role at our Central location

Purpose

The Clinical Research Coordinator I CRC I is an entry level research professional who supports the conduct of Phase II IV clinical trials under the direct supervision of the Principal Investigator PI and senior research staff. The CRC I assists with day to day study operations to ensure participant safety data integrity and compliance with the protocol Good Clinical Practice GCP Institutional Review Board IRB requirements and applicable regulatory guidelines.

This role serves as a key liaison between participants the research team and study sponsors contributing to high quality trial execution and audit readiness.

Essential FunctionsStudy Coordination
  • Supports the coordination of assigned clinical trials in accordance with the protocol ethical principles and regulatory requirements
  • Maintains working knowledge of study procedures visit schedules investigational product IP requirements and data collection processes
  • Assists with specimen collection labeling processing storage and shipment per protocol and laboratory standards
  • Communicates with central and local laboratories to resolve missing results or data discrepancies
  • Monitors study supply inventory and ensures equipment is functioning and calibrated as required
  • Participates in site initiation visits monitoring visits investigator meetings and required study training
  • Maintains documentation to support inspection readiness including version control of study materials
Participant Management
  • Assists with screening recruitment and enrollment of participants including obtaining HIPAA authorization and informed consent under PI supervision
  • Reviews medical records and pre screening information to assess eligibility escalates eligibility questions to the PI
  • Performs permitted clinical procedures for example vital signs phlebotomy ECGs and collects protocol required data
  • Educates participants on study procedures visit expectations device usage for example pumps and meters and safety considerations
  • Monitors participant adherence safety and well being throughout study participation
  • Documents all study activities in source documents and case report forms CRFs following Good Documentation Practices GDP
  • Supports investigational product management including receipt storage preparation accountability and destruction under PI or pharmacist oversight
  • Identifies documents and promptly reports adverse events AEs and serious adverse events SAEs in accordance with regulatory and sponsor requirements
  • Reviews participant diaries questionnaires and patient reported outcomes for completeness and protocol compliance
  • Provides a safe environment for participants and staff by adhering to OSHA CDC and institutional safety standards
Regulatory Compliance
  • Conducts study activities in accordance with ICH GCP E6 R3 emphasizing participant protection data reliability and risk based quality principles
  • Ensures timely communication of study updates safety reports and regulatory documents to the Regulatory Specialist for filing
  • Supports maintenance of essential documents and contributes to audit and inspection readiness
  • Follows institutional SOPs and reports deviations or non compliance to the PI and Quality Assurance team
Collaboration and Communication
  • Maintains clear timely communication with the PI regarding study progress participant concerns and protocol issues
  • Collaborates with the Director of Operations Regulatory Specialist QA Supervisor Data Entry Coordinators and other team members to ensure smooth study operations
  • Works closely with sponsor Clinical Research Associates CRAs during monitoring visits and supports resolution of data queries
  • Assists recruitment staff with implementing study specific recruitment strategies
  • Contributes to a positive collaborative team environment
Additional Non Essential Functions:
  • Assists other CRCs with participant visits as needed
  • Performs other duties as assigned to support study operations
QualificationsEducation & Experience RequirementsMinimum Required
  • Prior experience as a Clinical Research Coordinator or similar role in a medical setting
Preferred
  • Good Clinical Practice Certification
  • At least 2 years of experience as a Clinical Research Coordinator or similar role
  • Experience in diabetes and or endocrine clinical care or research
  • Prior patient care experience MALVNRN or similar
  • CPR AED certification
AAP/EEO Statement

Texas Diabetes and Endocrinology, P.A. TDE provides equal employment opportunities EEO to all employees and applicants for employment in accordance with applicable federal, state, and local laws. TDE complies with applicable state and local laws governing nondiscrimination in employment in every location in which it has facilities.

Other Duties

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

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