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Medical Content Writer

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  • Posted 3 months ago

Job Description

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 www.tagww.com to learn more.

Job Overview:

As Medical copywriter, you will play a central role in delivering copy needs for our Pharmaceutical client/s in the Taiwan market. Your focus will be to develop high-quality medical, copy and content solutions to help our pharmaceutical clients achieve their goals. This position requires strong background in medical and scientific writing, particularly in medico-marketing and marketing communications aimed at healthcare professionals (HCPs). As an ideal candidate, you will have at least 3 years medical writing experience in a pharmaceutical advertising agency including expert working knowledge of Veeva Vault PromoMats. You will excel at translating complex medical and pharmaceutical information into clear, engaging content.

Key Responsibilities:

Copy:

  • Create a wide range of HCP campaign materials, including websites, detail aids, leave behinds and emails.
  • Develop HCP educational content including slide decks, event invitations, workshops, and other educational materials.
  • Produce high-quality content across various formats, including print (brochures, posters, newsletters), digital (emails, e-learning modules), and audio-visual (educational videos, animations).
  • Customise content for diverse audiences, including healthcare professionals, patients, and regulatory authorities, while maintaining scientific integrity and regulatory compliance.
  • Originate new copy relevant to local launches or adapt content within a broader global strategy.
  • Develop content outlines, and storylines, and adapt materials to meet business objectives and campaign plans.
  • Liaise with clients and external stakeholders to create effective communication materials. Ensure smooth teamwork to achieve project goals and deadlines.
  • Manage own projects from first draft to delivery, working with studio teams to deliver on time, to brief and within budget.
  • Handle multiple projects simultaneously, ensuring timely completion and adherence to scope. Collaborate with peers and colleagues, reviewing and refining content to maintain high quality and effectiveness.

Governance:

  • Ensure all content maintains scientific rigour and accuracy.
  • Develop copy and content that adheres to industry guidelines (e.g. Medicines Australia Code of Conduct) with a strong understanding of regulatory compliance and ethical standards.
  • Stay up to date with the latest developments in healthcare, pharmaceuticals, and relevant therapeutic areas such as oncology, haematology, immunology, rheumatology, gastroenterology, neuroscience, and pulmonary arterial hypertension.
  • Manage the content approval process, including submissions to clients and regulatory bodies. Expertise in MLR approval processes and Veeva Vault PromoMats is mandatory.

Qualifications & requirements:

  • Master's degree in a relevant field (e.g., life sciences, pharmacy) is required. Advanced degrees (e.g, PhD) is 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. Ability to edit the content for language, grammar, standard styles, referencing styles etc.
  • Proficiency with industry-specific software and tools (e.g., Microsoft Office, EndNote, and reference management software, 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 the business need.

We offer 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.

Don't let self-doubt get in the way of what could be a great opportunity. We know from research that while men tend to apply to jobs when they meet around 60% of the criteria, women and people from diverse backgrounds may not put themselves forward unless they check every box.

If you think this role could be a great fit for you, please do 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.

(All information provided will be treated in strict confidence and used solely for recruitment purpose).

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Job ID: 134953635