Internship Program: Regulatory Affairs 

 

Position Summary: The Regulatory Affairs Intern will work with the Regulatory Affairs team in an effort to become familiar with the part Regulatory Affairs plays in the clinical trial process and pharmaceutical industry overall. The successful candidate will have the opportunity to utilize creative writing skills to both educate and make scientific “jargon” understandable to the reader. The successful candidate will gain an understanding of the liabilities and ethics of scientific writing.

Responsibilities:

  • Participate in document review and preparation for document submissions

  • Assist in document processing

  • Conduct literature searches and review for new product development

  • Schedule and coordinate internal and external regulatory meetings

  • Perform other functions as necessary or as assigned

Required Education, Qualifications and Experience:

  • Bachelor’s or Master’s Degree in life sciences

  • Language Proficiency: ILR Level 4 (Full professional proficiency) English language is required in both written and spoken English. Language proficiency will be tested.

  • Strong oral and written communication skills, as defined by the ability to:

  • understand grammar and syntax

  • be concise in writing and editing

  • identify relationships between ideas and organize them into logical sequence

  • Extremely detail-oriented

  • Ability to meet fixed writing deadlines

  • Strong MS Office skills

  • Ability to work effectively both independently and in a team environment

  • Must present documents showing legal authorization to work in the U.S.

To submit your CV for our consideration, please email us at jobs@amarexcro.com.

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