Clinical Research Coordinator

Prime Clinical Research Inc; Mansfield (TX); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Competitive hourly wage

Job summary

Prime Clinical Research Inc is seeking a skilled bilingual clinical research coordinator in Mansfield, TX. The ideal candidate will have a strong background in clinical research and phlebotomy, responsible for patient care and supporting clinical trials.

This full-time position offers responsibilities ranging from sample handling to patient education, with the opportunity to make a meaningful impact in medical research. A competitive hourly wage is provided based on experience.

Qualifications

• Demonstrated proficiency in phlebotomy techniques.
• Previous experience as a clinical research coordinator required.
• Strong understanding of medical terminology.

Responsibilities

• Perform venipuncture and capillary blood collection procedures.
• Greet patients and prepare them for medical procedures.
• Assist in the execution of clinical trials.
• Properly label and transport collected samples.
• Schedule appointments and manage patient records.
• Provide clear instructions for at-home care.
• Adhere to strict infection control protocols.
• Assist with outreach to potential research subjects.

Skills

Bilingual (Spanish and English)

Phlebotomy expertise

Excellent communication skills

Attention to detail

Interpersonal skills

Education

High school diploma or equivalent

Good Clinical Practice certification

Certified Phlebotomy Technician certification

Tools

Electronic health records (EHR)

Basic office software

Job description

Overview

We are seeking a bilingual (Spanish and English speaking), skilled and dedicated full-time clinical research coordinator to join our research team at Prime Clinical Research. The ideal candidate should have a strong background as a clinical research coordinator with expertise in phlebotomy. The clinical research coordinator will play a crucial role in providing exceptional patient care, performing phlebotomy tasks, and contributing to the smooth execution of research. This position offers an opportunity to make a meaningful impact on patients’ lives and contribute to advancements in medical research.

Key Responsibilities

• Phlebotomy Expertise: Perform venipuncture and capillary blood collection procedures with precision and care. Ensure patient comfort and safety during blood draws while maintaining sterile techniques.
• Patient Care: Greet and prepare patients for medical procedures, collect relevant medical history, and explain procedures clearly. Assist healthcare professionals in patient examinations, treatments, and minor procedures.
• Clinical Trials Support: Assist in the execution of clinical trials. Follow protocols, document procedures accurately, maintain compliance with regulatory requirements, and update CTMS. Collaborate with research staff to ensure smooth trial operations.
• Sample Handling: Properly label, process, and transport collected blood and other samples. Ensure accurate documentation and timely delivery of samples to the appropriate laboratory or testing facility.
• Administrative Tasks: Schedule appointments, manage patient records, and update electronic health records accurately and efficiently. Assist with billing and insurance processes as needed.
• Patient Education: Provide patients with clear instructions for at‑home care, medication administration, and follow‑up appointments. Address patient questions and concerns with empathy and professionalism.
• Infection Control: Adhere to strict infection control protocols to minimize the risk of cross‑contamination and maintain a safe healthcare environment.
• Recruitment: Assist and manage outreach to potential research subjects.

Qualifications

• High school diploma or equivalent.
• Current Good Clinical Practice certification.
• Certified Phlebotomy Technician (CPT) certification.
• Previous experience as a clinical research coordinator, with a demonstrated proficiency in phlebotomy techniques.
• Clinical trial experience is required.
• IATA/DOT Dangerous Goods training preferred but not required.
• Clear understanding of medical terminology and procedures.
• Excellent communication skills, both verbal and written.
• Strong interpersonal skills and the ability to work effectively within a multidisciplinary healthcare team.
• Attention to detail and strong organizational skills.
• Proficiency in using electronic health records (EHR) systems and basic office software.

Working Hours

This is a contracted position, with an estimated 40 hours per week. The schedule includes weekdays generally within working hours of 9AM to 6PM, with opportunities for additional work on weekends as well.

Location

Our primary office location is in Mansfield, but additional opportunities for more hours may become available as we expand across the DFW metroplex.

Benefits

Competitive hourly wage commensurate with experience.