Content Specialist at Who Collaborating Centre For Int Drug Monitoring
Uppsala, , Sweden -
Full Time


Start Date

Immediate

Expiry Date

01 Oct, 25

Salary

0.0

Posted On

02 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

Would you like to contribute to the safer use of medicines and vaccines for everyone everywhere? Join our team as a Content Specialist.
We are looking for a Content specialist to join our Drug Dictionary Management team within the Portfolio and Product Management department at UMC on a temporary, full time basis. The position will last a year, starting in the second half of August.
About the role
The Drug Dictionary Management team comprises health professionals with advanced education in the science of pharmacy who support the development and maintenance of the WHODrug portfolio, including WHODrug Global, the world’s most widely used drug dictionary. They ensure all information therein meets the highest quality standards, complies with regulations, and meets customer expectations in close cooperation with the WHODrug Portfolio management. The team is also involved in the development of processes and systems regarding generation of Pharmaceutical product ID (PHPID) and Global substance ID following the ISO Identification of medicinal products (IDMP) standards.

What you will do

  • Validate and classify drug information to ensure the completeness, accuracy and consistency of the data so that it meets the quality standards expected for WHODrug Coding of reported drugs in individual case safety reports and in clinical trials.
  • Take part in improvements to ways of working within the team.

Who you are
Do you have a MSc in Pharmacy, a knowledge of medicinal products as well as excellent written and oral skills in English? You may be the person we are looking for.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities
  • Validate and classify drug information to ensure the completeness, accuracy and consistency of the data so that it meets the quality standards expected for WHODrug Coding of reported drugs in individual case safety reports and in clinical trials.
  • Take part in improvements to ways of working within the team
Loading...