Associate Director - Medical Writing

Associate Director - Medical Writing

Job Title: Associate Director - Medical Writing
Contract Type: Permanent
Location: New Jersey, USA
Salary: Negotiable
Reference: 864895_1507058581
Contact Name: Reece Mitellas
Contact Email:
Job Published: October 03, 2017 20:23

Job Description

On behalf of SciPro's client located in the New Jersey area, I am interested in speaking with candidates who meet the majority of the description below in order to understand your interest to consider an Associate Director - Medical Writing position. If you feel you have the skills required, please do not hesitate to apply.

The Associate Director - Medical Writing will be the designated Lead Medical Writer for approximately 3 Neuroscience or General Medicine Programs, responsible for providing needed support and direction to other staff/contractors on these programs. As the lead writer, the incumbent ensures timely completion, accuracy, and quality of all clinical and submission documentation across all aspects of the compounds' lifecycle management. Due to the complexity of the programs, the incumbent must rapidly acquire complete and advanced knowledge of the compound to ensure alignment and consistency across studies. The qualified candidate will have proven ability to effectively manage the outsourcing of document preparation when necessary and the associated service providers.

Responsibilities Include But Are Not Limited To

  • Working on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors
  • Independently prepares and at times may direct, the writing of PCSs, protocols and protocol amendments
  • Independently prepares and at times may direct, all the writing of the CSRs including narratives
  • Works across functional areas to obtain all applicable source materials
  • Leads the preparation of clinical sections of submission documents, such as the briefing books, Global Investigator Brochures, and annual regulatory reports
  • Leads the medical writing activities for marketing application submission documents
  • Liaises with other functional areas and groups in the development of document standards and structure
  • Interacts routinely with clinical research and biostatistics staff to gain comprehensive understanding of the study design, and results across the program
  • Implements document quality controls, standards and best practices Job Qualifications - BS required/MS preferred
  • Minimum of 8 years medical writing experience in an industry setting, with specific experience with compounds in Neuroscience
  • Must have participated in or lead a major marketing application submission
  • Strong critical thinking and problem solving skills
  • Self-motivated with the ability to influence others
  • Ability to multitask on complex projects
  • Result driven with a mastery of time management and project planning
  • Able to work on site
  • Advanced working knowledge of MS project and MS Word

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