Expert database and computer skills, including Microsoft Word, Excel, and Outlook.
Knowledge of FDA regulations and Good Clinical Practices.
Ability to maintain data integrity and confidentiality.
Ability to work collaboratively with physicians, nurses, technicians, secretarial staff, and ancillary hospital staff.
Responsibilities
Participate in research participant screening, recruitment, and enrollment.
With oversight, consent participants and conduct research visits for no-risk or minimal-risk trials.
Collect, process, and ship research specimens where applicable.
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.
Organize trial-related documents and correspondence.
Implement quality control and quality assurance methods.
Assist with basic regulatory document preparation under oversight, including study amendments, adverse event reports, and protocol deviation reports.
Maintain professional and technical knowledge about clinical trials.
Communicate with research participants and their families.
Protect patient confidentiality.
Desired Qualifications
Phlebotomy certification is recommended.
Excellent verbal and written communication skills.
Ability to work independently and assume responsibility.
Excellent organizational skills.
Ability to meet data deadlines.
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
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.
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.
Regulatory and quality. Maintain organization of all trial-related documents and correspondence. Implement quality control and assurance methods.
Regulatory support. Assist with basic regulatory document preparation with oversight, e.g. study amendments, adverse event reporting, protocol deviation reporting.
Professional and technical knowledge. Maintain professional and technical knowledge about clinical trials.
Participant communication and confidentiality. Communicate with research participants and their families, and protect patient confidentiality.
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.