Medical Writer II - 1 year fixed term contract

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

Job summary

Join a leading clinical research organization as a Medical Writer, working with a Top-5 pharmaceutical company. This home-based role involves authoring regulatory documents and collaborating with stakeholders. Enjoy competitive benefits and opportunities for career growth.

Benefits

Health Insurance

Retirement Planning Options

Life Assurance

Childcare Vouchers

Gym Discounts

Qualifications

• At least 3 years of experience in writing regulatory documents.
• Familiar with submission processes.

Responsibilities

• Author study-level documents, including protocols and clinical study reports.
• Support experienced writers in preparing complex clinical documents.
• Interpret and summarize data effectively.

Skills

Communication

Problem-Solving

Stakeholder Management

Job description

Overview

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

This role is fully dedicated to a Top-5 pharmaceutical company. Working with our client, you will benefit from ICON's ongoing learning opportunities and the potential to develop a long-term career.

This is a home-based position in the UK or Europe, offered as a 1-year fixed-term contract.

Responsibilities

• Independently author study-level documents, ranging from simple to complex, including:
• Protocols and protocol outlines
• Subject Information/Informed Consent forms
• Clinical Study Reports (CSRs)
• Lay summaries of clinical trial results
• Investigator brochures (IBs)
• Support more experienced writers in preparing submission and other complex clinical documents.
• Interpret and summarize data effectively.
• Lead discussions, facilitate decision-making, and incorporate project strategies into documents.

Qualifications

You are:

• Experienced in writing regulatory documents for pharma or CRO, such as protocols, CSRs, IBs, with at least 3 years of experience.
• Familiar with submission processes or components thereof.
• A proactive team player.
• Skilled at building and maintaining stakeholder relationships.
• Engaged with stakeholders to understand and align on project goals, timing, and scope.
• Possessing strong communication, facilitation, and problem-solving skills to manage stakeholder interactions and drive decisions.

What ICON offers

Our success depends on our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. Alongside a competitive salary, ICON offers benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements
• Health insurance options
• Retirement planning options
• Global Employee Assistance Programme (TELUS Health)
• Life assurance
• Optional benefits like childcare vouchers, bike schemes, gym discounts, travel passes, and health assessments

Visit our careers website to learn more about working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are core to our culture. We are committed to providing an inclusive, accessible environment and a workplace free of discrimination and harassment. Qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If you require accommodations during the application process due to a medical condition or disability, please let us know via the provided form: https://careers.iconplc.com/reasonable-accommodations

Interested but unsure if you meet all requirements? We encourage you to apply—there’s a good chance you are exactly who we’re looking for, whether for this role or others at ICON.