Medical Writer Job at Hotwire (Sydney)

Medical Writer

AdMed is an award winning, integrated agency that designs and delivers modern tr...

Location

United States , Philadelphia

Salary:

Not provided

AdMed, Inc.

Expiration Date

Until further notice

Requirements

1 year of medical writing experience in a pharmaceutical, biotech, or medical education environment
Knowledge of AMA style
Attention to scientific accuracy and stylistic detail
Good understanding of anatomy, physiology, and pathophysiology
Experience in medical writing, referencing, review, and copy approval
Strong interpersonal skills
Ability to produce detailed, comprehensive documentation
Resourcefulness and attention to detail, with excellent follow-through skills
Excellent computer skills, including proficiency in Microsoft Office and Adobe Acrobat
Effective time management, flexibility, and comfort with meeting deadlines

Job Responsibility

Write outstanding, original scientific copy for a variety of target audiences
Generate ideas – individually, with colleagues, and with clients – to turn scientific facts into engaging video and cutting-edge training
Attend client meetings, listening to their needs, offering your feedback, and building a level of trust that will ensure future commitments
Guide team members as a content expert, helping artists, editors, and other writers bring your vision to life
Read and review educational content with precision, keeping the science in training accurate and the clients’ stylistic preferences adhered to
Dig into the details, researching and referencing, and always staying aware of current literature and guidelines
Take control of the material you write as an on-camera trainer in custom videos
Translate video training into a world of different formats, including print manuals, virtual training sessions, and web-based applications
Identify potential challenges in a project – including those caused by a client’s change to a project plan, timeline, or a request that is out of the scope of their contract – and spearhead possible resolutions

What we offer

401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance

Fulltime

Medical Writer

Guidepoint Insights enables clients to make better-informed decisions through in...

Location

India , Pune

Salary:

Not provided

Modoras Accounting Syd

Expiration Date

Until further notice

Requirements

Master’s degree (or PhD preferred) in Life Sciences, Public Health, or a related field
2+ years of experience in medical writing, healthcare research, or clinical/scientific communication
Ability to interpret and clearly present scientific and medical data for an investment audience
Strong command of written English
working knowledge of AP style and in-house editorial guidelines
Proficiency with Microsoft Office (Word, PowerPoint, Excel) and collaboration platforms
Strong organizational skills, meticulous attention to detail, and ability to meet deadlines in a fast-paced environment
Comfortable working across multiple healthcare subsectors and learning new domains quickly

Job Responsibility

Collaborate with analysts and moderators to develop clear, unbiased, and logically sequenced survey questions
Review survey responses from experts, synthesizing insights into slides and actionable takeaways
Monitor survey pipelines to ensure deliverables are on-time and aligned with quality standards
Contribute to the ongoing build-out of Guidepoint’s healthcare knowledge base

What we offer

Competitive compensation
Employee medical coverage
Central office location
Entrepreneurial environment, autonomy, and fast decisions
Casual work environment

Fulltime

Medical Writer

The Medical Writer applies basic to intermediate documentation preparation and d...

Location

United Kingdom , London

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor’s or higher degree preferred
scientific focus desirable
University-level medical or technical writing course(s) or equivalent experience in science/technical writing
Evidence of medical writing career development desirable, eg, American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association
Up to 2 years as a medical writer in the pharmaceutical industry or at least 5 years of medical or scientific writing experience as a primary job responsibility
Familiar with drug development process (discovery to market)
Basic understanding of biostatistical and clinical research concepts
Basic applied knowledge of documentation required for the conduct of clinical studies, protocol design, study results reporting
Writing high-quality documents that support corporate goals and objectives
Experience writing, reviewing, or editing protocols and clinical study reports preferred

Job Responsibility

Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
Aids in managing study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
Adheres to departmental procedures and practices and technical and industry standards during all aspects of work
Assists in developing and reviewing standard processes and templates within Global Medical Writing
Works effectively with cross-functional groups within BioMarin
Other tasks as assigned

Fulltime

Medical Writer

The Medical Writer 1 applies basic to intermediate documentation preparation and...

Location

United States , San Rafael

Salary:

74100.00 - 100000.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor’s or higher degree preferred
scientific focus desirable
University-level medical or technical writing course(s) or equivalent experience in science/technical writing
Evidence of medical writing career development desirable, eg, American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association
Up to 2 years as a medical writer in the pharmaceutical industry OR At least 5 years of medical or scientific writing experience as a primary job responsibility
Familiar with drug development process (discovery to market)
Basic understanding of biostatistical and clinical research concepts
Basic applied knowledge of documentation required for the conduct of clinical studies
Basic applied knowledge of protocol design
Basic applied knowledge of study results reporting

Job Responsibility

Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
Aids in managing study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
Adheres to departmental procedures and practices and technical and industry standards during all aspects of work
Assists in developing and reviewing standard processes and templates within Global Medical Writing
Works effectively with cross-functional groups within BioMarin
Other tasks as assigned

What we offer

discretionary annual bonus
discretionary stock-based long-term incentives
paid time off
company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Medical Writer

Are you ready to take the next step in your career as a Medical Writer? Are you ...

Location

United States

Salary:

Not provided

Oxford PharmaGenesis

Expiration Date

Until further notice

Requirements

12-18 months of experience in a writing-focused role in the medical communications sector
an advanced science degree, for example MS, PhD (preferably in life sciences), MD, PharmD or MPH
experience with scientific publications (e.g. writing a manuscript, congress presentation or similar)
the ability to communicate complex scientific ideas and data in a clear, concise and impactful way
the adaptability and flexibility to thrive in a fast-paced, dynamic environment
candidates must live in and have the right to work in the USA

Job Responsibility

work closely with clients and key opinion leaders, building strong professional relationships and contributing to high-quality scientific communications
work in publications and focused on oncology and neurology
creating abstracts and manuscripts

What we offer

exceptional learning opportunities
matched charitable fundraising
hybrid working approach (2 days per week in person for relationship building and collaboration)

Fulltime

Assistant Medical Writer

AdMed is an award winning, integrated agency that designs and delivers modern tr...

Location

United States , Philadelphia

Salary:

Not provided

AdMed, Inc.

Expiration Date

Until further notice

Requirements

Work closely with Content, Production, and Account Management teams to create medical training products and ensure medical accuracy
Create accompanying training products such as workbooks, virtual classrooms, visual summaries, assessment questions, and more
Ensure medical accuracy of products by reviewing scientific literature, textbooks, and prescribing information to support claims
Assists with developing and maintaining artificial intelligence and (AI) chatbots on pharmaceutical information
Work on multiple projects at a time and allocate time according to job priority
A passion for simplifying complex science for the broader public
Ability to accurately review complex materials including texts, graphics, audio, and videos with excellent attention to detail
Ability to work in a deadline-oriented environment
good organizational, multitasking, and prioritizing skills
Excellent team player

Job Responsibility

Work closely with Content, Production, and Account Management teams to create medical training products and ensure medical accuracy
Create accompanying training products such as workbooks, virtual classrooms, visual summaries, assessment questions, and more
Ensure medical accuracy of products by reviewing scientific literature, textbooks, and prescribing information to support claims
Assists with developing and maintaining artificial intelligence and (AI) chatbots on pharmaceutical information
Work on multiple projects at a time and allocate time according to job priority

What we offer

401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance

Fulltime

Principal Medical Writer, Patient Safety

Location

India , Remote, Bengaluru

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Strong analytical and problem-solving abilities, with the capability to independently evaluate complex data and draw meaningful conclusions
Exceptional communication skills, both verbal and written, including the ability to produce clear, concise, and accurate medical/scientific content
Excellent interpersonal and collaboration skills, fostering productive relationships with clients, cross-functional teams, and stakeholders
Effective organizational and prioritization skills, with the ability to manage multiple tasks enthusiastically and maintain attention to detail under tight timelines
Client-focused mindset, demonstrating flexibility, professionalism, and a proactive approach to meeting client expectations and expanding business opportunities
Strong negotiation and stakeholder management skills, ensuring alignment of resources, timelines, and deliverables across teams and departments
Cultural awareness and adaptability, enabling effective communication and collaboration in global, multicultural environments
Proficient in computer operations and IT tools, with expertise in web-based applications and familiarity with the Windows operating system and Microsoft Office suite (Word, Excel, PowerPoint)
Prior experience in pharmacovigilance, or related fields is preferred
Demonstrates Solid understanding of global pharmacovigilance regulations, medical terminology, and safety-related concepts

Job Responsibility

Independently lead the preparation/update of complex scheduled and unscheduled aggregate safety reports across multiple product types and regulatory regions
Serves as an SME for safety reports, developing templates, guiding teams, and creating strategies to address complex regulatory and data presentation challenges
Facilitate operational coordination, including scheduling and leading meetings, drafting agendas and minutes, tracking action items, and ensuring timely follow-up on open issues to support seamless project execution
Ensure compliance and quality across aggregate safety reports, performing detailed reviews for factual accuracy and internal consistency across documents
Manage the distribution of final reports to stakeholders, including partners, affiliates, and health authorities
Leads advanced safety signal detection and management for key products, integrating diverse data sources and innovative analytical approaches to identify emerging safety concerns
Provides expert interpretation of complex safety data patterns and trends across product lifecycles
Leads clinical safety activities for complex molecules, contributing to strategic decisions as part of the global safety team
Directs literature review strategies and critically evaluates scientific evidence for inclusion in safety documents
Leads safety evaluations for complex molecules and sensitive indications

Senior Medical Writer

Location

France

Salary:

Not provided

Product Life Group

Expiration Date

Until further notice

Requirements

Pharmacist or physician residing and operating in France
Minimum 5-8 years of experience in a PV department (preferentially in a Medical Writing department)
Well versed with Safety databases

Job Responsibility

Analysis of data and preparation of ad hoc reports/plans in the framework: PADER
Risk management plan
Benefit / risk evaluation report
Signal detection and reporting
PSUR / PBRER / Addendum to Clinical Overview
DSUR
Off label use reports (French requirements)
PSUSA response
Literature screening for medical writing reports
Ad hoc reports from regulatory authority

Fulltime

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