Regulatory Affairs Specialist (A Global Regulatory Affairs Lead Role - GRAL) Open in all the countries in Latin America

🔍 Buenos Aires, Argentina, Argentina

Sao Paulo, Brazil, Brazil Lima, Peru, Peru Bogota, Colombia, Colombia Santiago, Chile, Chile Mexico City, Mexico, Mexico

📁: Regulatory Affairs

📅   : Apr 30, 2019 Post Date

📅   : 14879 Total Views

Thanks for your interest in the Regulatory Affairs Specialist (A Global Regulatory Affairs Lead Role - GRAL) Open in all the countries in Latin America position. Unfortunately this position has been closed but you can search our 0 open jobs by clicking here.

Education and Experience:

Bachelor's Degree in Pharmacy or Life Science
2-3 years regulatory experience, or combination of higher education/less experience
Or substitution of equivalent relevant work experience

Knowledge, Skills and Abilities:

Broad regulatory affairs experience
Good interpersonal skills
Good knowledge Global Regulatory Affairs Procedures
Proven ability to work effectively in a team
A good knowledge of a number of country specific clinical trial application procedures Expert knowledge of ICH and global regulatory guidelines
Familiar with computers and their applications
Good organizational and planning skills
Must be able to work autonomously with minimal supervision
Planning skills
Mental skills required in areas of reading and interpretation of data, numeracy, language, analytical, investigative, verbal and written communication, customer contact, attention to detail, multiple project tasking

Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by federal, state, and/or local law.