Phlebotomist/Lab Tech

Revival Research Institute, LLC; Denton (TX); On-site; USD 25,000 - 36,000; Part time

Job summary

Revival Research Institute, LLC in Denton, TX is seeking a part-time Phlebotomist/Lab Tech with at least 1 year of clinical experience to draw and process research specimens and support study visits under oversight.

You will assist Investigators and clinical staff, manage sample handling, data entry in case report forms, and ensure confidentiality while maintaining compliance with FDA regulations and GCP guidelines.

Qualifications

• Phlebotomy skills required; certification recommended.
• Minimum of 1 year of clinical experience.
• Knowledge of FDA Regulations and Good Clinical Practices.

Responsibilities

• Screen, recruit, enroll participants and collect specimens.
• Document study data in case report forms or EDC systems.
• Maintain trial documents and ensure quality control.
• Assist with regulatory document preparation and adverse event reporting.
• Communicate with participants and protect confidentiality.

Skills

Phlebotomy

Data entry

Verbal communication

Tools

Microsoft Office

Outlook

Job description

About Revival Research Institute

Revival Research Institute, LLC has been conducting industry-sponsored clinical trials since 2015. Headquartered in Metro Detroit, we operate sites across Michigan, Texas, Illinois, New Jersey, and North Carolina, and have been recognized nationally for the quality of the data we deliver to our sponsors.

About This Role

This is a part-time position. We are hiring a Phlebotomist/Lab Tech with a minimum of 1 year of clinical experience who can draw and process research specimens and support study visits with oversight.

Phlebotomists/Lab Techs at Revival support the Investigators and other clinical staff with study-related tasks including, but not limited to:

Responsibilities

1. Screening, recruitment, and enrollment. Participate in research participant screening, recruitment, and enrollment. Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight. Collect, process, and ship research specimens, where applicable.
2. Data and monitoring. Document study-related information in case report forms or electronic data capture systems, handle data queries, and participate in monitoring visits. Obtain, review, and maintain source documents.
3. Regulatory and quality. Maintain organization of all trial-related documents and correspondence. Implement quality control and assurance methods.
4. Regulatory support. Assist with basic regulatory document preparation with oversight, e.g. study amendments, adverse event reporting, protocol deviation reporting.
5. Professional and technical knowledge. Maintain professional and technical knowledge about clinical trials.
6. Participant communication and confidentiality. Communicate with research participants and their families, and protect patient confidentiality.

Preferred Qualifications

1. Phlebotomy skills required; certification recommended.
2. Minimum of 1 year of clinical experience.
3. Expert database and computer skills: Microsoft Office (Word, Excel), Outlook; excellent verbal and written communication skills; ability to work independently and assume responsibility; excellent organizational skills; ability to meet data deadlines and maintain confidentiality. Maintain data integrity within the department. Must be able to work in a team consisting of physicians, nurses, technicians, secretarial staff, and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices.