← all jobs

PK Medical Writer

Work from home Full-time role Hiring

This a Full Remote job, the offer is available from: Europe, European Union, EMEA, Greece, Poland, Romania, Portugal, Spain, United Kingdom, Sweden, Austria, France, Italy PK Medical Writer 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. 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. Expectations:

  • Write clear and concise documents, including study reports, protocols 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. Visit our careers site to read more about the benefits ICON offers. 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. Are you a current ICON Employee? Please click here to apply This offer from "ICON plc" has been enriched by Jobgether.com and got a 0% flex score.

More open positions

Associate Medical Writer, Market Access

Work from home Full-time role

Coordinator - VIP Marketing at Hard Rock Digital: 100% Remote (MI, IL, OH, IN)

Work from home Full-time role

Remote SEO Project Manager / Marketing Project Manager

Work from home Full-time role

Social Media Manager, Prequel (Remote) - $60,000/year USD

Work from home Full-time role

Paid Social Manager (Remote US) - Future Opening

Work from home Full-time role

Physical Design Engineer

Work from home Full-time role

Associate Inside & Digital Sales Representative

Work from home Full-time role

Install Base Account Executive - Enterprise

Work from home Full-time role

MSAT Strategy & Deployment Director

Work from home Full-time role

Quality Assurance Analyst

Work from home Full-time role

UI/UX Design Lead

Work from home Full-time role

🌟 Join the Stars: Licensed Life & Health Insurance Agent 🌟

Work from home Full-time role

SAP Hybris + SAP Spartacus | Brillio | Remote

Work from home Full-time role

Remote Patient Monitoring Clinical Manager- Centralized Monitoring Unit

Work from home Full-time role

Project Accountant - Remote

Work from home Full-time role

Sales Development Representative

Work from home Full-time role

Desenvolvedor de Sistemas – Full Stack - SR - 1

Work from home Full-time role

Technical translator with Swedish [Job Vacancy ID: ST7]

Work from home Full-time role

Nurse Case Manager II

Work from home Full-time role

Quality Improvement Specialist

Work from home Full-time role

SEO Strategist

Work from home Full-time role