Klick is hiring a

Bilingual Medical Editor (Freelance)

Toronto, Canada
Contractor
About our Medical Craft
Our Science & Regulatory team, as part of Klick's Medical Craft, is pivotal in ensuring the highest standards of scientific accuracy and regulatory compliance in healthcare communications. This dedicated group of medical writers, editors, and regulatory affairs experts meticulously reviews every piece of content, ensuring it aligns with industry regulations and contributes to better health outcomes. By joining this team, you will be part of a culture that values excellence and supports the advancement of medical marketing through evidence-based strategies and communications.

As a Medical Editor you’ll work with a team of top performers to help design and deliver digital marketing sites, media, apps, and other projects. Everyone at Klick wears a lot of hats and you’ll be no exception. Your day could include anything from proofreading to attending regulatory reviews and everything in between. You’ll have a lot of support from the best leadership team in Canada and tons of opportunities to learn from the smartest team in digital marketing. 

You’ll be busy, but you’ll love it because you’ll be doing amazing work with amazing people. Klick is a special place. We have a rare and special culture that we defend and cherish. We work in a beautiful office, filled with smart and dedicated people who are committed to delivering healthier outcomes for our clients’ patients. We work hard but we play hard too. Klick is intentionally unlike any agency you’ve ever encountered. It’s hard to get a job here. But it’s really worth it.

Minimum qualifications:

  • 3+ years experience in a similar role
  • Background in science or pharma
  • Confidence in your ability to flawlessly proofread content in both French and English
  • Experience submitting to ASC and PAAB
  • Extreme attention to detail
  • Bonus: experience and understanding of Veeva Promomats

Responsibilities:

  • Editing, fact-checking and proofreading clinical and patient-focused content.
  • Attending inter-departmental meetings, regulatory review meetings and/or client calls.
  • Regulatory submission preparation and content change management.
  • Maintaining style guides and core claims documents.
  • Acting as a regulatory compliance consultant

#LI-LP2 #LI-Hybrid
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