Clinical Research Intern I

doTERRA International LLC•Pleasant Grove, UT

About The Position

At doTERRA we encourage all employees to seek out opportunities that will expand their skill set. We strive to help achieve personal career goals by providing opportunities of growth and movement throughout the company.

Requirements

Ability to communicate and write effectively
Excellent organizational, analytical, and teamwork skills
Willing to take instruction, follow directions and learn new processes
Self-starter with ability to work with minimal supervision in identifying research gaps
Ability to manage multiple ongoing projects concurrently and meet deadlines
High school diploma required
Experience in Excel, Word, and PowerPoint required

Nice To Haves

Bachelor’s degree (or working toward) in any field preferred
Experience in laboratory work, data entry, and/or scientific method preferred

Responsibilities

Collaborate and assist in new research project ideas
Assist in study design and implementation
Write research proposals, protocols, and completion reports
Collect, read, and summarize scientific papers relevant to dōTERRA research
Enter and analyze data from research projects
Undergo training on all applicable protocols and protocol-associated documents
Undergo training in research ethics, Good Clinical Practice, HIPAA laws, and all other applicable subjects
Process human blood, tissue, urine, or other biological samples as directed in approved clinical research protocols
Maintain meticulous records of sample collection, labeling, storage, handling, and disposition
Aid in designing and carrying out laboratory experiments as needed
Perform other responsibilities as directed