Medical Content Writer

1 day ago

hong kong, Hong Kong SAR China Tag Full time

3 days ago Be among the first 25 applicants

Senior People & Culture Business Partner HK & TW at Tag

At Tag, we bring big ideas to life. As a leading creative production and sourcing partner, we work with some of the world’s biggest brands and agencies, delivering content at scale to create campaigns that are more impactful, more effective and more efficient.

We believe that the combination of different ideas, experience, backgrounds and skillsets create a great place to work, and we are committed to promoting an inclusive, equitable and diverse culture where each employee feels supported and empowered.

But don’t just take our word for it We are proud to have recently won awards for Best Culture, Production Agency of the Year and Outstanding SME in Gender Equality, Family Status Equality and Racial Equality and Inclusion. Check out to learn more.

Job Overview:

The ideal candidate should have a strong background in medical and scientific writing, especially the medico-marketing/marketing communications. He/she should have a deep understanding of the pharmaceutical, life-sciences, medical devices and healthcare industry, and the ability to understand complex information and create clear and engaging content.

As a Medical Communications Content Writer, he/she will play a critical role in our efforts to deliver high-quality communication materials that support our clients' goals.

Key Responsibilities:

  • Content Development: Ability to read and understand the project brief, guide the content writers and cross-functional teams on scope of work. Research, write, and edit a wide range of medical communication materials, including scientific manuscripts, medical marketing collateral, and educational content. Candidates should have a complete knowledge on the different types of marketing collaterals and best practices in creating such engaging content. He/she must be able to create content outline, storyline, and create/adapt the content to align with business/marketing objectives, campaign plans, and communication objectives. Review and proof-read the content for quality & accuracy.
  • Scientific Accuracy: Ensure the accuracy, integrity, and scientific rigor of all content by staying up-to-date with the latest developments in healthcare, pharmaceuticals, and relevant therapeutic areas.
  • Audience Adaptation: Write/adapt/customize the content to diverse target audiences, including healthcare professionals, patients, and regulatory authorities, while maintaining scientific integrity and regulatory compliance.
  • Collaboration: Collaborate with cross-functional teams, including medical experts, graphic designers, digital coding experts, project managers, clients & client servicing teams, to produce cohesive and effective communication materials.
  • Regulatory Compliance: Adhere to industry guidelines, regulatory requirements, and ethical standards to ensure all content meets the highest standards of quality and compliance.
  • People & Project Management: Manage multiple projects simultaneously, ensuring that they are completed on time and within scope. Work closely with peers & colleagues from the content writing team; review the content created by fellow team members.
  • Feedback Integration: Incorporate feedback from clients and internal stakeholders to continually improve and refine content.
  • Content Approval Support: Should be aware of different types of submissions involved in content approval by clients/regulatory bodies/healthcare authorities preferably in the US and UK. Knowledge on the submission process in other regions including the EU, Middle East & Asian markets is a plus. Hands-on experience with Veeva Vault Promo Mats is mandatory.

Qualifications & Requirements:

  • Master’s degree in a relevant field (e.g., life sciences, pharmacy) is required. Advanced degrees (e.g., PhD) are a plus.
  • ≥3 years of experience in medical communications (preferably medico-marketing/promotional content), medical writing, or a related field.
  • Strong understanding of the pharmaceutical and healthcare industry, including knowledge of clinical trials, drug development, regulatory processes, and marketing activities.
  • Exceptional writing and editing skills, with the ability to convey complex scientific concepts in a clear and engaging manner.
  • Proficiency with industry-specific software and tools (e.g., Microsoft Office, EndNote, Veeva Vault, Aprimo, etc).
  • Strong attention to detail and ability to work independently or as part of a team.
  • Knowledge of industry guidelines, including ICH-GCP, PhRMA, and CONSORT, is a plus.
  • MUST be ready to work in different time zones as per business needs.

We offer a competitive remuneration package and fringe benefits to the successful candidate. In addition, you will have an opportunity to work in a reputable company with excellent career exposure.

Interested parties please send us your full resume with expected salary and availability by clicking "Easy Apply".

As an ethical employer, Tag will never ask job applicants to provide private, sensitive information upfront or make offers of employment contingent on financial requests or responsibilities from any candidate.

If you think this role could be a great fit for you, please get in touch – even if you don’t meet every single requirement. Let’s have a chat and see if this could be the right role for you.

Seniority Level

Associate

Employment Type

Full-time

Job Function

Writing/Editing and Advertising

Industries

Media Production

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