Medical Writer II

ICON Clinical Research; Swansea; Remote; GBP 55,000 - 90,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

LifeWorks

Life assurance

Flexible benefits

Job summary

ICON Strategic Solutions seeks a Senior or Principal Medical Writer to lead the creation of regulatory and clinical documents, guiding writing strategy and coordinating writers for major submissions. Join a sponsor-dedicated team supported by ICON’s global expertise.

You will contribute expertise on regulatory content and formats, support cross-functional teams, and act as a key writer for regulatory responses, with leadership responsibility across development programs.

Qualifications

• Bachelor’s degree in science or health required.
• 3+ years of pharma/biotech writing experience with electronic submissions.
• Experience writing key documents such as Clinical Study Reports, IBs, and Protocols.

Responsibilities

• Lead writing strategy, timelines, and resource planning for regulatory submissions.
• Coordinate assignments to writers and perform substantive editing and review.
• Prepare documents for submissions to regulatory authorities and ensure regulatory compliance.

Skills

Writing leadership

Regulatory writing

ICH guidelines

Communication skills

Education

Bachelor’s degree in science

Job description

Medical Writer II

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

We are currently seeking Senior or Principal Medical Writer to join our diverse and dynamic team. At this role you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. Your expertise in medical writing will be crucial in supporting our clients’ submissions to regulatory authorities and ensuring compliance with industry standards.

We hire at Medical Writer 2, Senior Medical Writer or Principal Medical Writer level

What You Will Be Doing:

Guides medical writing document preparation, including coordination of assignments to writers, review, and substantive editing of documents. As necessary, may assume primary responsibility for preparation of key regulatory response documents and documents supporting major regulatory submission. Formulates writing approach, develops timelines, and assesses resource requirements for key documents and regulatory submissions within designated therapeutic or functional area. Participates on relevant project teams and task forces, and provides functional and cross-functional guidance on a wide range of issues related to document preparation, including international regulatory guidance and requirements for content and format, work requirements (style, electronic integrity, and process), and project- or therapeutic area-specific guidance related to content and organization of specific documents.

• Leads the writing strategy providing expertise including organization, content, timelines, and resource requirements.

• Provides more complex advanced input for study designs, analysis plans, sections of INDs and marketing applications

• Provides review and substantive editing of contributions, and ensures resolution of issues.

• Within designated therapeutic or compound function, manages deliverables and preparation of documents for submission to regulatory agencies, ensuring consistency of content within therapeutic areas and adherence to regulatory requirements and Sponsor requirements and processes across development programs.

• Represents Medical Writing on cross-functional teams and task forces (related to projects, process, and standards).

• Acts as a key Medical Point of contact for clinical regulatory strategy

• As required, serves as lead writer for important regulatory response documents and key components of regulatory submissions.

• Provides leadership on functional teams that address requirements or issues related to document preparation and production.

• The Principal Medical Writer is seen as an expert in medical writing and performs work independently with minimal supervision.

Your Profile:

• Bachelor’s degree in science, health profession required

• At least 3 years of experience writing for pharma or biotechnology preferred . 3+ years of electronic documents and submissions required.

• Experience with writing key documents like Clinical study reports, IBs, Protocols

Knowledge and Skills:

• Clear understanding of clinical development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission and support for marketed products.

• Understanding of international regulations, ICH guidelines, and applicable international regulatory processes related to document preparation and production (including CTDs).

• Well-developed oral and written communication skills; ability to clearly present technical information within and across functional areas.

• Demonstrated problem-solving and interpersonal skills that facilitate effective interactions within functional and cross-functional teams and with external providers

#LI-NR1 #LI-Remote

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements

• A range of health insurance offerings to suit you and your family’s needs.

• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

• Life assurance

• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)