Phlebotomist/Lab Tech

Revival Research Institute, LLC; Dallas (TX); On-site; USD 21,000 - 30,000; Part time

Job summary

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

The role involves assisting investigators and clinical staff with recruitment, data collection, and regulatory tasks while maintaining participant confidentiality and data integrity.

Qualifications

• Phlebotomy skills required; certification recommended.
• Minimum of 1 year of clinical experience.
• Excellent verbal and written communication; ability to work independently and maintain confidentiality.

Responsibilities

• Screening, recruitment, and enrollment of participants with oversight.
• Document study data and handle data queries in CRF/EDC systems.
• Maintain trial documentation and support regulatory quality processes.
• Assist with basic regulatory document preparation and study amendments.
• Maintain professional knowledge of clinical trial practices.
• Communicate with participants and protect confidentiality.

Skills

Phlebotomy

Clinical data collection

Communication skills

Tools

Microsoft Word

Microsoft Excel

Microsoft 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.