Senior Medical Writer - single sponsor dedicated

Pharmaceutical Research Associates, Inc; United Kingdom; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading clinical research organization is seeking a Medical Writer to produce regulatory documents for top pharmaceutical companies. This remote role requires at least 3 years of experience in writing clinical study documents, with a focus on stakeholder engagement and communication. Join us to advance your career while enjoying benefits like health insurance and flexible perks.

Benefits

Health insurance options

retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible benefits like childcare vouchers

Qualifications

• At least 3 years of experience in writing regulatory documents.
• Familiarity with submission processes.
• Proactive team player skilled in building relationships.

Responsibilities

• Independently author study-level documents including protocols and clinical study reports.
• Support experienced writers with complex clinical documents.
• Interpret and summarize data effectively.
• Drive discussions and support decision-making.

Skills

Regulatory document writing

Stakeholder management

Communication skills

Problem-solving

Job description

Overview

As a Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Medical Writer you will be fully dedicated to a Top-5 pharmaceutical company. While working for our client, you will be able to profit from ICON through continued learning opportunities and building a longer-term career.

This role is home based in the UK or Europe.

Responsibilities

• Independently author study-level documents, including protocols, subject information/informed consent, clinical study reports (CSRs), lay summaries, and investigator brochures (IBs).
• Support more experienced writers with complex clinical documents and submissions.
• Interpret and summarize data effectively.
• Drive discussions, support decision-making, and incorporate project strategies into documents.

#LI-Remote

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Qualifications

You are:

• Experienced in writing regulatory documents for pharma or CRO (protocols, CSRs, IBs) with at least 3 years of experience.
• Familiar with submission processes or components thereof.
• A proactive team player skilled in building stakeholder relationships.
• Excellent in stakeholder engagement, communication, and problem-solving to manage interactions and drive decisions.

What ICON can offer you: Our success relies on our people. We prioritize a diverse culture that rewards high performance and nurtures talent. Benefits include:

• Various annual leave entitlements
• Health insurance options
• Retirement planning options
• Global Employee Assistance Programme with TELUS Health
• Life assurance
• Flexible benefits like childcare vouchers, gym memberships, and more.

Visit our careers website for more: https://careers.iconplc.com/benefits

ICON is committed to inclusion and providing an accessible environment for all candidates. We ensure equal opportunity employment regardless of race, religion, gender, or disability. For accommodations during the application process, please contact us.

Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly what we're looking for.