Research Assistant

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
• Rapidly growing team with opportunities for advancement
• Competitive compensation
• Benefits package

Duties you will be responsible for:

• Provide 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.
• Perform activities in accordance with established policies and procedures related to clinical research study protocols, including answering phone calls, screening participants for eligibility, and registering subjects in Real Time.
• Organize the lab and maintain inventory of clinical supplies such as lab kits and phlebotomy supplies.
• Assist in ensuring that study materials and lab kits are shipped and resupplied as requested.
• Support members of study/project teams; review source documents, clinical procedures, and draft new procedures or revisions.
• Participate in ongoing clinical and study-specific training.
• Communicate as necessary with vendors and supporting functions at the site level.
• Attend investigator meetings as required or requested by the PI and Clinical Research Coordinator.
• Compile source documents for active studies and ensure source binders contain appropriate documentation for screening upcoming patients.
• Collect data as required by the protocol.
• Assure timely completion of source documents.
• Process and ship labs.
• Assist in EDC completion.
• Complete study documentation and maintain study files in accordance with sponsor requirements and procedures.
• Maintain effective and ongoing communication with the PI, Clinical Research Coordinators, and research participants during the course of the study.
• Work with the PI under the Clinical Research Coordinator to manage day-to-day activities of the study including problem-solving, communication, and protocol management.
• Assist 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.

We thank you for your interest in joining our growing Gastro Health team!