Top 41 Phlebotomy Jobs in Beaumont, Tx

Clinical Research Coordinator
Gadolin Research —Beaumont, TX
- $42,000 - $52,000 a year
- Full-time
- Background check
- Nursing
- Microsoft Outlook
- Health insurance
- Dental insurance
Quick Apply
Clinical Laboratory Scientist II - Lab AdminGeneral
Christus Health —Beaumont, TX
- PRN
- No experience needed
- Bachelor's degree
- Pediatrics
13d
Clinical Laboratory Scientist II - Lab AdminGeneral
Christus Health —Port Arthur, TX
- PRN
- No experience needed
- Bachelor's degree
- Pediatrics
Clinical Laboratory Scientist II - Lab AdminGeneral
Christus Health —Beaumont, TX
- Full-time
- No experience needed
- Bachelor's degree
- Pediatrics
6d
Clinical Laboratory Scientist I, Lab AdminGeneral, Mid County - PRN
Christus Health —Port Arthur, TX
- PRN
- No experience needed
- Bachelor's degree
- Pediatrics
5d
Phlebotomist
Grifols —Beaumont, TX
- Full-time
- High school diploma or GED
- Ability to lift 50 pounds
- Entry level
Phlebotomist - mobile collections
LIFESHARE BLOOD CENTER —Beaumont, TX
- $14.42 - $16.50 an hour
- Weekends as needed
- CPR Certification
- BLS Certification
- No experience needed
- Wellness program
- Disability insurance
Patient Services Technician
PathGroup —Beaumont, TX
- High school diploma or GED
- Entry level
- Travel reimbursement
Quick Apply
1d
Phlebotomist - Lab AdminGeneral
Christus Health —Beaumont, TX
- Full-time
- Spanish
- Customer service
- Pass drug screening
16h
Phlebotomist III Float
Quest Diagnostics —Beaumont, TX
- From $22.25 an hour
- Full-time
- Private practice
- Customer service
- 5 years
- Employee stock purchase plan
- Disability insurance
Quick Apply
9d
Phlebotomist
Medical Center SE Texas Port Arthur —Port Arthur, TX
- Full-time
- BLS Certification
- High school diploma or GED
- Hospital experience
Quick Apply
Phlebotomist II
Quest Diagnostics —Port Arthur, TX
- From $20.23 an hour
- Overtime
- Clean driving record
- Sanitation
- English
- Employee stock purchase plan
- Disability insurance
Quick Apply
9d
Medical Assistant (Full-time)
Diana Health —Beaumont, TX
- Full-time
- Vital signs
- High school diploma or GED
- Clinic
- Paid parental leave
- Health savings account
Quick Apply
9d
Apheresis Tech
LIFESHARE BLOOD CENTER —Beaumont, TX
- $13.42 an hour
- Serving
- OSHA
- Customer service
Center Supervisor
Biolife Plasma Services —Beaumont, TX
- $22.80 - $31.35 an hour
- Full-time
- CPR Certification
- Ability to walk for extended periods
- BLS Certification
- Paid holidays
- Disability insurance
Emergency Department Technician - Emergency Department
Christus Health —Beaumont, TX
- Full-time
- BLS Certification
- High school diploma or GED
- Computer skills
7d
Medical Assistant - Baptist Cancer Center - Oncology - Days
Baptist Hospitals of Southeast Texas —Beaumont, TX
- CPR Certification
- Vital signs
- Hospital
- Health insurance
- Dental insurance
13d
Medical Technician
Business Health Partners —Nederland, TX
- From $14 an hour
- Full-time
- Background check
- Vital signs
- Computer literacy
- Health insurance
- Dental insurance
Quick Apply
3d
Lead Medical Assistant
Centerwell —Port Arthur, TX
- $48,300 - $65,900 a year
- Full-time
- Spanish
- CPR Certification
- Vital signs
- Paid parental leave
- Paid holidays
Medical Assistant - PRN - Vidor
Texas MedClinic —Vidor, TX
- Part-time
- Vital signs
- BLS Certification
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply

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phlebotomy jobs near beaumont, tx

Clinical Research Coordinator

Gadolin Research
Beaumont, TX

Quick Apply

Job Details

Full-time
$42,000 - $52,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Phase II clinical trials
CCRC
Clinical research
Operations coordination
Research project coordination
Bachelor's degree
Phase I clinical trials

Full Job Description

**Interested applicants must be able to interview onsite in Beaumont, TX with 1 day notice. No AI resumes.**

Position Summary

At Gadolin Research, Clinical Research Coordinators (CRCs) are central to our mission of advancing science while delivering patient-centered care. Guided by our ICROP values — Integrity, Commitment to Accountability, Relentless Improvements, Ownership Mindset, and Patient-Centeredness — the CRC manages study operations, ensures compliance, supports participants, and maintains the highest quality standards in clinical research.

Core Responsibilities

Study Operations & Integrity

Review study protocols with the PI, evaluating feasibility and site resources.
Coordinate and conduct study visits, including informed consent, eligibility, procedures, and follow-up.
Support study start-up and close-out activities, ensuring compliance with ICH-GCP, FDA, IRB, and site SOPs.
Serve as a resource for participants, caregivers, and sponsor/CRO staff.

Regulatory & Accountability

Work with the regulatory coordinator to prepare and submit IRB applications and amendments.
Act as the day-to-day liaison with the IRB and Human Research Committee.
Ensure consistency and compliance across all regulatory documents.
Participate in protocol operations manual development and adherence.

Data Management & Relentless Improvements

Accurately enter, verify, and monitor study data in eSource, EDC, CTMS, IWRS/IRT, and related systems.
Implement quality control measures to ensure accuracy, completeness, and audit readiness.
Organize and maintain research databases, extracting information for reports,

publications, and sponsor monitoring.

Recommend workflow enhancements that improve efficiency and compliance.

Ownership Mindset & Collaboration

Take ownership of assigned studies from screening through database lock.
Collaborate with physicians, investigators, and site staff to ensure smooth protocol implementation.
Mentor new coordinators and contribute to a culture of accountability and teamwork.
Assist PI with manuscript preparation, data graphics, and presentations for internal and external audiences.

Patient-Centered Care

Recruit, screen, and enroll participants, ensuring a positive and supportive experience.
Educate participants and caregivers on trial requirements, procedures, and safety expectations.
Monitor participant well-being and report adverse events promptly.
Promote retention through compassionate engagement and flexibility.

Skills & Competencies

Technical Skills

Proficiency with Microsoft Office Suite, Outlook, and database systems.
Experience with EDC, IWRS/IRT, ePRO, CTMS, and eSource platforms preferred.
Familiarity with ICH-GCP E6(R2), HIPAA, safety monitoring, and human subject protections.

Clinical Skills (Preferred, Not Required)

Vital signs, ECG, phlebotomy, medical history, and medical terminology.

Abilities & ICROP Competencies

Integrity: Uphold ethical standards and accuracy in all trial activities.
Commitment to Accountability: Meet timelines, maintain documentation, and ensure compliance.
Relentless Improvements: Identify opportunities to improve site operations and workflows.
Ownership Mindset: Manage responsibilities proactively and independently.
Patient-Centered: Prioritize participant dignity, safety, and satisfaction.
Analytical problem-solving skills with initiative to introduce innovations.
Strong organizational, communication, and interpersonal skills.
Ability to manage multiple priorities and meet deadlines in a fast-paced environment.

Qualifications

Bachelor’s degree required (life sciences, nursing, or related field).
Research experience preferred, but strong healthcare or clinical background will be considered.
Certification (CCRC or equivalent) preferred but not required; training opportunities available.

Work Environment

Clinical office and patient care setting with routine standing, walking, and sitting.
Handling biological samples and medical supplies required.
Occasional travel for training or sponsor meetings.

Job Type: Full-time

Pay: $42,000.00 - $52,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance

Education:

Bachelor's (Required)

Experience:

research coordination: 1 year (Required)

Ability to Commute:

Beaumont, TX 77702 (Required)

Work Location: In person

Quick Apply

Refine Your Search

phlebotomy jobs in beaumont, tx

Clinical Research Coordinator

Clinical Laboratory Scientist II - Lab AdminGeneral

Clinical Laboratory Scientist II - Lab AdminGeneral

Clinical Laboratory Scientist II - Lab AdminGeneral

Clinical Laboratory Scientist I, Lab AdminGeneral, Mid County - PRN

Phlebotomist

Phlebotomist - mobile collections

Patient Services Technician

Phlebotomist - Lab AdminGeneral

Phlebotomist III Float

Phlebotomist

Phlebotomist II

Medical Assistant (Full-time)

Apheresis Tech

Center Supervisor

Emergency Department Technician - Emergency Department

Medical Assistant - Baptist Cancer Center - Oncology - Days

Medical Technician

Lead Medical Assistant

Medical Assistant - PRN - Vidor

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