Pk Medical Writer

Icon Clinical Plc; Milano; In loco; EUR 70.000 - 95.000; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive base salary

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes

Learning and development opportunities

Descrizione del lavoro

ICON is a global healthcare intelligence and clinical research organisation. ICON seeks a PK Medical Writer to lead medical writing strategies for CPP documents, CSRs, protocols, and other regulatory documents within global procedures.

You will drive document preparation, review statistical outputs, and ensure deliverables are inspection-ready while collaborating with cross-functional teams and regulatory agencies as needed.

Competenze

• 3–5 years of medical writing experience in the pharmaceutical/biotech/CRO industry.
• Strong writing, editing and proofreading skills with ability to summarize complex data.
• Solid understanding of regulatory requirements (ICH-GCP, FDA, EMA) and ability to interact with regulators.

Mansioni

• Lead development and execution of medical writing strategies for CPP documents and related submissions.
• Write clear, concise study reports, protocols, and publications with input from teams.
• Drive document preparation, review statistical outputs, and distribute for review while addressing reviewer comments.
• Provide scientific writing consultancy to project teams and ensure deliverables meet SOPs and regulatory standards.
• Maintain planning and QC of population PK/PD documents and related deliverables.

Conoscenze

Medical writing

Regulatory knowledge

Editing and proofreading

Data interpretation

Scientific communication

Project management

Stakeholder collaboration

Formazione

Advanced degree in Life Sciences, Pharmacy, Medicine, or related field

Descrizione del lavoro

PK Medical Writer

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Senior Medical Writer at ICON, you will lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies.

Purpose

Deliver high quality relevant Clinical Pharmacology Pharmacometrics (CPP) documents (e.g. population PK/PD data transfer plans, population PK/PD analysis plans and population PK/PD reports), as well as CSRs, protocols, and other documents, within the required regulatory system per global aligned procedures of the client.

Documents that the writer will be doing include

CSRs for phase 1 healthy volunteer trials and clinical pharmacology trials. Protocols for healthy volunteer studies. Module 2.7.1 and 2.7.2.

Expectations

Write clear and concise documents, including study reports, protocols, investigator brochures, summary documents, and other scientific documents. Drive the document preparation process, receive and review primary statistical output, draft and distribute documents for review, and incorporate/resolve comments with all reviewers. Provide scientific and medical writing consultancy to project teams, as requested.

Deliverables

Services rendered will adhere to applicable client’s SOPs, WIs, policies, local regulatory requirements, ICH-GCP, etc. Clear communication with clinical pharmacology pharmacometrics leaders and other team members. Ensure deliverables are inspection ready and compliant with relevant requirements. Maintain the central planning of population PK/PD document writing and QC deliverables.

Your profile

Advanced degree in Life Sciences, Pharmacy, Medicine, or related field, with a minimum of 3-5 years of experience in medical writing within the pharmaceutical, biotechnology, or contract research organization (CRO) industry. Proficiency in interpreting and summarizing complex clinical trial data, scientific research findings, and statistical analyses, with excellent writing, editing, and proofreading skills, and the ability to communicate scientific concepts to diverse audiences. Strong understanding of regulatory requirements (e.g., ICH-GCP, FDA, EMA) governing the preparation and submission of clinical documents and publications, and experience in interacting with regulatory agencies during the review and approval process. Demonstrated ability to work effectively in a fast-paced, deadline-driven environment, managing multiple projects simultaneously and prioritizing tasks based on project timelines and deliverables. Excellent interpersonal and communication skills, with the ability to collaborate effectively with cross-functional teams, build relationships with key stakeholders, and influence decision-making processes.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Summary

Location: UK, Reading; France, Paris; Spain, Madrid; Bulgaria, Sofia; Austria, Vienna; Portugal, Lisbon; Greece, Athens; Poland, Gdansk; Italy, Milan; Ireland, Dublin; Sweden, Lund. Type: Full time