Phlebotomist/Lab Tech

Revival Research Institute, LLC•Cary, NC

1d•Onsite

About The Position

Revival Research Institute, LLC, established in 2015 and headquartered in the Metro Detroit Region, has grown to have a national presence across several states. The institute is recognized for providing high-quality data for clinical research trials. As Revival Research Institute expands, it seeks qualified professionals to join its team and grow with the company. This full-time Phlebotomist/Lab Tech position requires a minimum of 1 year of clinical experience. While a strong interest in the Clinical Research field is a plus for this entry-level role, it is not mandatory. The ideal candidate is detail-oriented, capable of maintaining organized records, and motivated to learn new things as the company explores new therapeutic areas. Phlebotomists/Lab Techs at Revival Research Institute are expected to be respectful of diverse viewpoints and contribute to an inclusive environment that fosters productivity. They will assist Investigators and other clinical staff with various study-related tasks.

Requirements

Minimum of 1 year of clinical experience.
Detail orientated, being able to maintain organized records.
Motivated to learn new things.
Genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results.
Phlebotomy skills required.

Nice To Haves

Strong interest in the Clinical Research field.
Phlebotomy Certification recommended.
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.

Responsibilities

Participates 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.
Responsible for collecting, processing and shipping of research specimens, where applicable.
Documents study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits.
Obtain, review and maintain source documents.
Maintains organization of all trial related documents and correspondence.
Implement quality control and assurance methods.
Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting.
Maintain professional and technical knowledge about Clinical trials.
Research participant/family communication, protect patient confidentiality.