Medical Writer - Onsite

Job Type:
Contract
Sector:
Medical Information
Job Category:
Medical Writing
Region:
USA
Area:
New Jersey
Location:
Unspecified
Salary Description:
Competitive
Posted:
30/11/2016
Job Ref:
lbbonsite

Regulatory Medical Writer - Onsite in New Jersey

This position will report to the Head of Medical Writing.  Experienced Regulatory Writer with a background in NDAs, ECDs, and CSRs.

  • Advanced degree in the life sciences required (eg, PhD).
  • Ability to quickly learn and grasp new therapeutic areas with an excellent ability to interpret and present scientific and clinical trial data, as well as understand complex statistical analyses.
  • Outstanding interpersonal and communication skills, with the ability to work well both independently and as part of a team.
  • Demonstrated initiative and the ability to handle a variety of projects simultaneously and productively with minimal supervision.
  • Exemplary writing skills coupled with a comprehensive knowledge of the drug development process and regulatory guidelines.
  • Meticulous attention to detail.
  • 3 years or more of direct biotechnology or pharmaceutical industry experience as a medical writer. Oncology writing experience is preferred.
  • Proficient with computer software applications, in particular document management software.

Please Call Lisa Bourbeau at 646-415-8221 or email at lbbourbeau@barringtonjames.com

Contact Details:
Tel: 919-838-7478
Contact: Lisa Bourbeau
Email:

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