Medical Writing QC Specialist Copenhagen

1 month ago

København, Denmark Globant Full time
Medical Writing QC Specialist Copenhagen

We are a digitally native technology services company where innovation, design and engineering meet scale. We use some of the latest technologies in the digital and cognitive field to empower organizations in every aspect.

Vertic, Globant division is currently looking for a Medical Writing QC Specialist to join its Globant Gut Studio in Copenhagen.

The Medical Writing QC Specialist will work closely with our team of medical writers and editors, reviewing and validating written content for scientific accuracy and consistency. This role requires a diligent eye for detail, a strong grasp of the pharmaceutical industry, the ability to interpret complex scientific data, and familiarity with medical terminology. As regulations and advancements within the pharmaceutical industry evolve, the ability to stay informed and adapt is crucial.

You will get the chance to:

  • Review and verify written content for medical accuracy, readability, and appropriacy of scientific data.
  • Ensure all content aligns with the relevant regulations, guidelines, and ethical standards.
  • Maintain consistency and accuracy in scientific data, medical terminology, and use of brand names across all materials.
  • Collaborate closely with medical copywriters and editors to address any identified issues or discrepancies.
  • Provide final quality approval for all content before it is published or submitted to clients.
  • Keep abreast with pharmaceutical regulations, industry trends, and medical advancements.
  • Participate in ongoing training and workshops to enhance skills and industry knowledge.

What will help you succeed:

  • Bachelor's degree in a scientific or medical field; advanced degree preferred.
  • Prior experience in medical writing, editing, or quality control, preferably within a pharmaceutical, medical, or advertising setting.
  • Comprehensive knowledge of medical terminology.
  • Understanding of pharmaceutical regulations and guidelines (e.g., FDA regulations).
  • Strong written and verbal communication skills.
  • Proficiency in using various software tools and databases relevant to the role.
  • Highly organized, and able to manage multiple tasks and projects.
  • A meticulous eye for detail and a commitment to producing high-quality work.
  • Strong scientific and medical knowledge, capable of interpreting complex data.
  • Familiar with regulatory guidelines and ethical standards in the pharmaceutical industry.
  • An excellent communicator, comfortable providing feedback and insights to team members.
  • Able to work in a fast-paced environment, managing multiple projects simultaneously.
  • Continually driven to learn and stay updated with the latest industry trends and advancements.
  • A strong team player, able to collaborate effectively with various teams and stakeholders.

At Globant we believe that an inclusive culture and a diverse environment makes us stronger. We encourage people to have an inclusive spirit as our global footprint expands.

Are you ready?

#J-18808-Ljbffr

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