sr. technical writer in bothell

posted
job type
contract
salary
US$ 80 per hour
apply now

job details

posted
location
bothell, washington
job category
Information Technology
job type
contract
salary
US$ 80 per hour
reference number
632389
phone
.
apply now

job description

job summary:

We are looking for a Sr. Technical Writer for an opportunity in Bothell, WA

The Technical Writing Consultant III role will be responsible for performing Clinical Evaluations and writing/updating Clinical Evaluation Reports (CERs), associated documents, templates, and processes in compliance with MEDDEV 2.7.1 Rev. 4 and the European Medical Device Regulation (MDR). The candidate should have excellent written and verbal communication skills, possess a strong sense of responsibility and urgency and have a minimum of 5 years direct experience performing clinical evaluations and writing CERs compliant with MEDDEV 2.7.1. This position requires the ability to interpret data from scientific literature and clinical studies and summarize the results and in a clear, concise, and scientifically accurate manner in the CER.

 
location: Bothell, Washington
job type: Contract
salary: $80 - 90 per hour
work hours: 8 to 5
education: Bachelors
 
responsibilities:
  • Perform Clinical evaluations and writing/updating Clinical Evaluation Reports (CERs), associated documents, templates, and processes in compliance with MEDDEV 2.7.1 Rev. 4 and the European Medical Device Regulation (MDR).
 
qualifications:
  • Excellent written and verbal communication skills.
  • Possess a strong sense of responsibility and urgency.
  • Have a minimum of 5 years direct experience performing clinical evaluations and writing CERs compliant with MEDDEV 2.7.1.
 
skills:
  • Ability to interpret data from scientific literature and clinical studies and summarize the results and in a clear, concise, and scientifically accurate manner in the CER.
  • If a candidate has this specific experience they will be a fit for the role as the experience will already be in place based off of doing this type of work before.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

skills

  • Ability to interpret data from scientific literature and clinical studies and summarize the results and in a clear, concise, and scientifically accurate manner in the CER. 
  • If a candidate has this specific experience they will be a fit for the role as the experience will already be in place based off of doing this type of work before.

qualification

  • Excellent written and verbal communication skills.
  • Possess a strong sense of responsibility and urgency.
  • Have a minimum of 5 years direct experience performing clinical evaluations and writing CERs compliant with MEDDEV 2.7.1.

responsibilities

  • Perform Clinical evaluations and writing/updating Clinical Evaluation Reports (CERs), associated documents, templates, and processes in compliance with MEDDEV 2.7.1 Rev. 4 and the European Medical Device Regulation (MDR).

educational requirements

Bachelors