Clinical Research Assistant — Entry-Level Trials

Iterative Scopes; Flowood (MS); On-site; USD 35,000 - 52,000; Full time

Job summary

Iterative Health is seeking a Research Assistant to support on-site clinical trial activities under the direction of the Principal Investigator and site management. This role involves participant screening, enrollment, data entry, documentation, and ensuring compliance with sponsor and GCP requirements.

The ideal candidate will be detail-oriented, possess healthcare experience, and collaborate with a study team to maintain study files and timelines throughout the trial lifecycle.

Qualifications

• High school diploma or equivalent; some college coursework preferred.
• At least 2 years of healthcare setting experience.
• Strong written and verbal communication skills.
• Ability to read, interpret, and apply clinic policies and research protocols.
• Proficiency in standard office software; familiarity with CTMS or eCRF platforms a plus.
• Highly organized with the ability to manage multiple tasks and meet deadlines.
• Ability to work both independently and collaboratively as part of a research team.

Responsibilities

• Assist the Study Team with communicating study requirements to all individuals involved in the study.
• Work with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB requirements.
• Assist with screening subjects for eligibility using protocol-specific inclusion and exclusion criteria...
• Assist with registering participants in the Clinical Trial Management System (CTMS) to ensure proper billing of study procedures to the appropriate funding source.
• Collect and report ongoing patient recruitment and enrollment progress and metrics to site management and the PI.
• Assist the Study Team in completing study documentation and maintaining study files in accordance with sponsor requirements and site policies...
• Enter all patient visit data in eCRF and CTMS on a daily basis or as directed.
• Arrange secure storage of study documents in accordance with GCP guidelines or the contracted length of time.
• Maintain inventory of study supplies; follow sponsor protocol and site policies on investigational drug/device accountability.
• Process and ship specimens per study protocol and IATA regulations as directed.
• Work with the Study Team to manage the day-to-day activities of the study, including problem-solving, communication, and protocol management.
• Aid the Study Team in maintaining effective and ongoing communication with sponsors, research participants, site management, and the PI throughout the course of each study.
• Assist the Study Team in protecting the rights and welfare of all human research participants in accordance with federal regulations.
• Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI; report instances of noncompliance to the appropriate compliance office.
• Perform job related duties as requested

Skills

Healthcare experience

Data entry

Communication skills

Organized

Confidentiality and data integrity

Education

High school diploma

Tools

CTMS

eCRF

Job description

Iterative Health is seeking a Research Assistant to support on-site clinical trial activities under the direction of the Principal Investigator and site management. This role involves participant screening, enrollment, data entry, documentation, and ensuring compliance with sponsor and GCP requirements.

The ideal candidate will be detail-oriented, possess healthcare experience, and collaborate with a study team to maintain study files and timelines throughout the trial lifecycle.