Research Assistant

Gastro Health; Cincinnati (OH); On-site; USD 35,000 - 50,000; Full time

Benefits offered by this job

Paid holidays

Paid time off

Competitive compensation

Benefits package

Job summary

Gastro Health in Cincinnati, Ohio is looking for a Full-Time Research Assistant to join their collaborative team. This role entails providing administrative support in clinical research settings, following federal regulations and research protocols, while ensuring effective communication within study teams.

The ideal candidate should possess a High School Diploma and preferably have research experience. Enjoy a work-life balance with no weekends or evenings, plus benefits and opportunities for advancement.

Qualifications

• Research experience preferred.

Responsibilities

• Assist Clinical Research Coordinators and local site with compliance tasks.
• Organize lab and maintain inventory of supplies.
• Collect and process data as per study protocols.

Education

High School Diploma

Job description

Gastro Health is seeking a Full-Time Research Assistant to join our team!

Gastro Health is a great place to work and advance in your career. You'll find a collaborative team of coworkers and providers, as well as consistent hours.

This role offers:

• A great work/life balance
• No weekends or evenings – Monday thru Friday
• Paid holidays and paid time off
• Rapidity growing team with opportunities for advancement
• Competitive compensation
• Benefits package

Duties you will be responsible for:

• General Administrative Provides assistance to Clinical Research Coordinators, local site, and Central Hub in accordance with federal regulations and sponsoring agency policies and procedures in compliance with Good Clinical Practice.
• Performs activities in accordance with established policies and procedures related to clinical research study protocols, including but not limited to: answering phone calls, screening participants for eligibility, and registering subjects in Real Time.
• Responsible for organizing the lab, and maintaining inventory of clinical supplies such as lab kits, phlebotomy supplies.
• Assist in ensuring that study materials and lab kits are shipped and resupplied as requested.
• Supports members of study/project teams; reviews source documents, reviews clinical procedures, drafts new procedures or revisions to existing procedures.
• Participate in ongoing clinical and study specific training.
• Communicates, as necessary with vendors and supporting functions at site level.
• Any other task assigned by the Clinical Research Coordinators and Central Hub Protocol Preparation & Review
• Attends investigator meetings as required or requested by the PI and Clinical Research Coordinator.
• Responsible for compiling source documents for active studies and ensuring source binders contain the appropriate documentation to screen upcoming patients. Prepares other study materials as requested necessary.
• Collects data as required by the protocol.
• Assures timely completion of Source Documents.
• Responsible for processing and shipping labs.
• Responsible for assisting in EDC completion.
• Completes study documentation and maintains study files in accordance with sponsor requirements and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.
• Maintains effective and ongoing communication with the PI, Clinical Research Coordinators, and research participants during the course of the study.
• Supports members of study/project teams; reviews source documents, reviews clinical procedures, drafts new procedures or revisions to existing procedures.
• Works with the PI under the Clinical Research Coordinator to manage the day to day activities of the study including problem solving, communication and protocol management.
• Project Closeout Assists the Principal Investigator,
• Clinical Research Coordinator and Regulatory Specialist with archival of study records in accordance with federal regulation, Gastro Health Research policies, and sponsoring agency policies and procedures.

Minimum Requirements

• High School Diploma
• Research experience preferred

Gastro Health is proud to be an Equal Opportunity Employer. We do not discriminate based on race, color, gender, disability, protected veteran, military status, religion, age, creed, national origin, gender identity, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law.