Akebia is seeking a summer intern to work with the Research Quality team. The individual will have the opportunity to explore the role of Quality in drug development including Good Laboratory Practices (cGLP) and current Good Clinical and Pharmacovigilance Practices (cGCP, cGPV). This is anticipated to be a 12-week internship and located in our Cambridge, MA offices.
Review audit reports and track flow of information and follow-up
Participate in the review and QC of data and/or reports generated from various departments
Assist with the maintenance of record keeping
Help with the tracking of key timelines and milestones
Perform related duties as requested
Currently enrolled in a B.S. or M.S. program at an accredited university and in good academic standing
Sound working knowledge in Microsoft Office
Effective communication skills with detailed focus and eager to learn
Must be authorized to work in the United States without visa sponsorship by Akebia
"Akebia Therapeutics, Inc. is a fully integrated biopharmaceutical company focused on the development and commercialization of therapeutics for patients with kidney disease. The company was founded in 2007 and is headquartered in Cambridge, Massachusetts. For more information, please visit our website at www.akebia.com."
Akebia Therapeutics is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.
Akebia Therapeutics, Inc.