Clinical Research Intern

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 for growth and movement throughout the company.

• 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

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

doTERRA International, LLC. is committed to employing a diverse workforce. Qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, protected veteran status, or disability.