Report Coordinator - Life Science Technical Writer

Covance Inc Located in: Chantilly,  Virginia
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Covance Inc Biotechnology Jobs Pharmaceutical Careers
 

JOB DESCRIPTION

Covance Report Coordinator - Life Science Technical Writer

 

Covance's BioAnalytical team is looking for a Report Coordinator/Technical Writer to join their team in Chantilly, VA. 

The Report Coordinator documents and generates bioanalysis study reports, analyzes results tables, and corresponds in a fast-paced, deadline-oriented environment. You must have good writing skills; the ability to take broad laboratory data and, using a template, correctly format, insert, and edit the data; and proficency with Microsoft Word and Excel. 

 

Specific responsibilities include:

  • Track project status for multiple ongoing studies using a variety of software applications/databases and laboratory information management systems (LIMs)
  • Prepare data tables which includes completing basic statistical analysis in table generation programs and compiled data tables
  • Create the study report using details described in the protocol and protocol
  • amendments and Covance or client-specific requirements
  • Incorporate contributions (protocol, amendments, certificates of analysis, contributor reports) into a draft report
  • Address quality assurance (QA) inspection items
  • Print, bind, and mail draft and final study documents
  • Prepare shipping paperwork for study documents
  • Schedule and coordinate study report finalization efforts
  • Prepare report amendments

 

 

  • Bachelor's degree in science, or a related field, preferred
  • Ability to utilize word processing software, database, spreadsheet, and specialized software
  • Skilled in concise writing which requires little to no external review or editing
  • Proficency in grammar, punctuation, composition, and spelling
  • Minimum of 2 years of study coordination experience or scientific writing experience or a combination of education, training, and experience
  • Excellent communication, presentation, and interpersonal skills
  • Excellent attention to detail
  • Ability to prioritize and manage time
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CRITICAL REQUIREMENTS

COMPANY INFORMATION

Covance Inc. is proud to be the only drug development company with a full range of research and development services—from lead optimization, to commercialization and life cycle management. Covance, headquartered in Princeton, NJ, is the drug development business of LabCorp with global operations in more than 30 countries.

JOB INFORMATION

Seniority Level:
Experienced - Not Management
Function:
  Medical Writing
Preferred Industry Background:
 
Managing a team of:
N/A
Required Travel:

Base Salary:
Confidential
Bonus:
Benefits:
Other Compensation: