Medical Writer Job at Hotwire (Sydney)

Medical Writer

We are currently looking for a Medical Writer or Senior Medical Writer to be at ...

Location

United Kingdom , Manchester / Macclesfield / London

Salary:

Not provided

Bioscript Group

Expiration Date

Until further notice

Requirements

Minimum 15 months medical writing experience in an MedComms agency
Evident writing skills and a passion for communicating complex ideas backed up with strong customer focus
Meticulous attention to detail and the ability to distil complex information for diverse audiences
A proactive approach to learning and staying informed about industry trends
Enthusiasm for working in a collaborative and dynamic environment

Job Responsibility

Translating complex scientific data into clear, concise, and accessible content
Collaborating with cross-functional teams to create compelling narratives to push the boundaries of medical science
Ensuring adherence to industry guidelines and regulatory standards
Conducting thorough research to stay abreast of the latest medical advancements
Developing educational materials and promotional content that help to bring the next generation of medicines to patients around the world

What we offer

25 days holiday + bank holidays + winter shutdown + holiday purchase scheme
Enhanced sick and compassionate leave
Enhanced maternity, paternity & adoption leave
Birthday charity donation to a charity of your choice
Bonus Day off to be spent giving back to the community
Life Insurance and Critical Illness cover
Private Medical (Vitality for UK based colleagues)
Health cash plan or wellbeing allowance
International Employee Assistance Program

Scientific and Medical Writer

Job opportunity for a Scientific and Medical Writer M/F. Permanent position base...

Location

France , Paris

Salary:

Not provided

AB SCIENCE

Expiration Date

Until further notice

Requirements

Post-graduate science degree in a biomedical field
previous medical or scientific writing experience
ability to analyse and summarise data from a diverse range of indications
advanced scientific writing skills
experience in the preparation of marketing authorisation applications and regulatory responses would be advantageous
fluency in written and spoken English

Job Responsibility

medical writing of all types of regulatory and clinical study documentation including Investigators’ Brochures, clinical study reports and protocols
preparation of regulatory responses to health authorities
preparation of marketing authorisation applications (eCTD module 2)
simultaneously manage several projects and meet tight deadlines

What we offer

salary package to define according to skills and experience

Fulltime

Medical Writer

We are looking for individuals to write and edit clinical documents to support r...

Location

Malta , Marsa

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

BS or MS in scientific or clinical discipline with excellent writing skills
2 years of on-the-job experience in scientific/medical writing preferred but not mandatory
knowledge of computer software Microsoft Word and Adobe Acrobat products
Microsoft Project and Visio are a plus
experience in scientific and/or medical writing
experience in the analytical evaluation of scientific data and written or oral presentation in a logical, clear, concise manner
strong organizational skills and meticulous attention to detail
familiarity with clinical trial-related and regulatory clinical submission templates and documents
apply global regulatory authority regulations and/or guidance
manage multiple projects with competing priorities

Job Responsibility

Develop high quality clinical documents ensuring scientific excellence and regulatory compliance
write, interpret and summarize clinical and non-clinical data
compile information and ensure delivery within timelines
ensure compliance of clinical documents with Baxter procedures, national and international regulatory requirements and guidelines
collaborate with cross functional team members and serve as MW representative at study team meetings
prepare document timelines, with guidance from manager, as needed
develop knowledge of one or more Baxter therapeutic areas.

Medical Writer

The Medical Writer position with PrimeVigilance offers an opportunity to further...

Location

United Kingdom , Guildford

Salary:

Not provided

PrimeVigilance

Expiration Date

Until further notice

Requirements

PhD or MSc in Life Sciences or Healthcare (pharmacy, biology, chemistry, veterinary medicine)
Previous experience of drug safety medical writing, including PBRERs, DSURs, RMPs
Time management, organisation and multitasking skills with good attention to detail
Strong communication and presentation skills
Advanced knowledge of MS Office
Fluency in English

Job Responsibility

Author Medical Writing tasks including aggregate reports, RMPs and other documents needed throughout the product’s life cycle
Responsible for the quality and content of the document, and quality control review of documents prepared by Medical Writing peers
Continuous self-education in all aspects associated with Medical Writing activities
Active participation in trainings, maintenance, and development of quality system documents
Support in all PV operations associated with Medical Writing

Medical Writer, Scientific Communications

The Medical Writer, Scientific Communications is responsible for writing strateg...

Location

United States

Salary:

70000.00 - 85000.00 USD / Year

Vaniam Group

Expiration Date

Until further notice

Requirements

PhD in life sciences, MD, or PharmD
At least 1 year of work experience in an agency, the pharmaceutical industry, or a related scientific or medical writing position
Working knowledge of digital marketing
Commitment to ethical and transparent data dissemination standards
Demonstrated ability to work collaboratively in a dynamic team environment
Excellent interpersonal, organization, verbal, and written communication skills
Excellent quantitative and analytical skills and ability to synthesize complex or diverse information
Excellent problem-solving skills
Strong attention to detail and listening skills
Ability to meet tight deadlines and have excellent time management skills

Job Responsibility

Develop high-quality content for an array of projects, including publications (eg, abstracts, presentations, and manuscripts), advisory boards, scientific platforms, gap analyses, literature summaries, slide sets, and training materials
Develop materials that are grammatically accurate and audience appropriate
Gain an understanding of the treatment landscape and strategic positioning of client products to help produce strategically aligned materials
Assess project needs and challenges
identify and implement solutions to meet productivity, quality, and client goals while maintaining compliance standards
Participate in client meetings and answer questions about projects when necessary
Build strong partnerships with and understand the importance of meeting the needs of internal teams
Work on multiple projects concurrently, prioritizing appropriately
Collaborate with team to execute project and meet deadlines
Emerging ability to assess areas for opportunity and improvement

What we offer

100% remote environment with opportunities for local meet-ups
Positive, diverse, and supportive culture
Investment in you with opportunities for professional growth and personal development through Vaniam Group University
Health benefits – medical, dental, vision
Generous parental leave benefit
Focused on your financial future with a 401(k) Plan and company match
Work-Life Balance and Flexibility
Flexible Time Off policy for rest and relaxation
Volunteer Time Off for community involvement
Emphasis on Personal Wellness

Fulltime

Medical Writer

The healthcare industry requires that we abide by regulations from all around th...

Location

Malta , Marsa

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

BS or MS in scientific or clinical discipline with excellent writing skills
2 years of on-the-job experience in scientific/medical writing (e.g., clinical trial and regulatory documents) preferred but not mandatory
Knowledge of computer software Microsoft Word and Adobe Acrobat products
Microsoft Project and Visio are a plus
Experience in scientific and/or medical writing
Experience in the analytical evaluation of scientific data and written or oral presentation in a logical, clear, concise manner
Strong organizational skills and meticulous attention to detail
Familiarity with clinical trial-related and regulatory clinical submission templates and documents
Apply global regulatory authority regulations and/or guidance
Manage multiple projects with competing priorities

Job Responsibility

Develops high quality clinical documents ensuring scientific excellence and regulatory compliance
Writing, interpreting and summarizing clinical and non-clinical data
Compiling information and ensuring delivery within timelines
Ensure compliance of clinical documents with Baxter procedures, national and international regulatory requirements and guidelines
Collaborate with cross-functional team members and serve as MW representative at study team meetings
Prepare document timelines, with guidance from manager
Develop knowledge of one or more Baxter therapeutic areas

Senior Healthcare Content Writer

Our client, a leader in the healthcare insurance space, is seeking a highly skil...

Location

United States , Atlanta

Salary:

Not provided

Tier4 Group

Expiration Date

Until further notice

Requirements

A Bachelor’s degree, preferably in English, Journalism, Marketing or communications
Minimum of 7-10 years’ experience
Corporate experience with the ability to interact with C-level executives
Superior creative and technical writing and grammar skills
Experience in medical or healthcare communications and writing with a strong understanding of medical terminology and healthcare industry practices
Proven ability to translate complex analyses into engaging, clear, and impactful content
Understanding of SEO and writing meta data, keywords, and alt text
Knowledge of MS Office applications including Word and PowerPoint
Openness to a rapidly changing and growing environment
A self-starter that’s able to work both independently and collaboratively on multiple projects concurrently

Job Responsibility

Research and write articles, white papers, reports, presentations, courses, and other content primary for the website, but channels also could include print, video, social, email, and more
Work with analytics team to highlight liability risk and incorporate analytics insights throughout content
Edit learning content developed by medical and legal faculty
Collaborate with the Chief Medical Officer, Director, Advice Content Strategy, and subject matter experts to research and develop ideas for new content
Work closely with the marketing team to optimize copy for digital channels, including SEO
Deliver work that reflects a careful attention to detail and adherence to legal and brand guidelines

Fulltime

Technical Writer

PaxeraHealth, a medical imaging and AI software development industry leader work...

Location

Egypt , Cairo

Salary:

Not provided

PaxeraHealth

Expiration Date

Until further notice

Requirements

Bachelor's degree or equivalent in English, Technical Writing, Journalism, Marketing/Communications, or related field
Two years of experience as a Technical Writer responsible for writing, publishing, and managing help content
Experience synthesizing feedback and input from multiple stakeholders
Excellent written and verbal communication skills with a strong attention to detail
Proven experience prioritizing writing projects and activities in a time-constrained setting with simultaneous deadlines
Must be proficient in document development and management software skills including Microsoft Office, Adobe, HTML
Must have demonstrated analytical and problem-solving skills and have the ability to effectively and independently manage a large workload with minimal supervision
Ability to navigate ambiguity and driving toward clarity and solutions

Job Responsibility

Understands and accurately translates technical information for a general audience and various healthcare, clinical, and medical imaging application user personas
Plans, develops, organizes, writes, proofreads, and edits written materials such as application guides, system manuals, product release notes, product integration guides, conformance statements, specifications, and other product and operational documentation
Produces dynamic, electronic documentation in addition to hard copy manuals
Maintains a comprehensive library of technical terminology and documentation
Analyzes and formats documentation to maintain continuity of content style
Manages timely updates and revisions to technical literature
Determines the needs of end users of technical documentation
Uses photographs, drawings, diagrams, animation, and charts that increase users understanding of content
Creates scripts for video tutorials
Creates comprehensive user assistance documentation, including how-to sections, FAQs, and Help sections

Fulltime

Medical Writer

Hotwire

Location:
Australia , Sydney

Category:
-

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 18, 2026

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Job Posted:February 18, 2026

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