Research Assistant

This role

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

• 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.
• Aid 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.
• Communicates, as necessary with vendors and supporting functions at site level.
• Any other task assigned by the Clinical Research Coordinators and Central Hub

Attends investigator meetings

• Compiles source documents for active studies and ensures source binders contain the appropriate documentation to screen upcoming patients.
• Collects data as required by the protocol.
• Assures timely completion of Source Documents.
• Processes and ships labs.
• 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

• 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.

Requirements

• High School Diploma
• Research experience preferred

Benefits

• Comprehensive benefits package

About the role

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.