Responsibilities: 
Independently plan and prepare a variety of clinical documents to support all phases of
clinical pharmaceutical development. 
Manage and coordinate document technology issues so that submission documents can be
electronically prepared. 
Participate on all levels of project-related teams, and assist with development of timelines
and resource plans for clinical sections of regulatory submissions or for implementation of
communication strategy. 
Coordinate/conduct document-related meetings, lead a Clinical Registration team, represent the
department at meetings, and participate in process improvement initiatives is essential. 
Requirements: 
BS/BA + 8 years or a MS/MA or PharmD + 6 years or a PhD + 6 years of relevant technical or
medical writing experience. 
You must have a strong understanding of global pharmaceutical regulatory requirements and
ideally experience in Anti-Viral clinical research. 
Ability to accurately and clearly present clinical data as well as strong verbal, written and
interpersonal communication skills a must. 
Idenix offers an excellent benefits package including competitive salary, equity compensation,
major medical insurance, dental insurance, 401(k) plan participation, and group life and
disability insurance. 

To be considered for this position, please send your resume by email to [email protected] , or by
mail to:

Human Resources
Idenix Pharmaceuticals
60 Hampshire Street
Cambridge, MA 02139 
www.idenix.com 

Email: [email protected]