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Medical Writer I

Do you have a passion for scientific writing and clinical research? Then, join Fortrea as our next Medical Writer 1 and help ensure new medicines are safe for patients while kick-starting a global career in clinical trials. As a Medical Writer 1 you will play a key role mobilizing cross-functional teams in the development of essential clinical documents for early phase clinical trials (I-IIa), with a focus on safety and pharmacokinetics. LOCATION As one of the largest Clinical Research Organizations (CROs) in the world, we have four Early Phase Clinical Research Units in the UK and US… and the jewel in the crown is our facility at Drapers Yard Leeds. A brand new, world class, state-of-the-art 65,000 ft² Phase I clinic only 7 minutes walking from the train station. This is a full-time, permanent job, with a hybrid work model: Combining some remote work with regular office presence for training and teamwork. Ideal for candidates living in or around Leeds. WHAT YOU WILL DO Learn the science behind Medical Writing You will learn how to develop the documents that enable the conduct of a clinical trial and to analyze the data that will help the sponsor to decide the future of their molecule. With on-the-job training and guidance from your colleagues and managers, by the end of your first year, success means you'll be able to: Drive the development of simple design Protocols and Clinical Study Reports (CSRs) with minimal supervision, Navigate the fast-paced timeliness of the document development cycle. This includes: Critically reviewing and interpreting clinical research data (particularly Pharmacokinetics and safety), Condensing data and conclusions into clear concise language in Protocols and CSRs. Project Manage the document development cycle from start to final deliverable You´ll be the nexus where multiple teams´ expertise converge. You will coordinate and collaborate with multiple stakeholders, steer discussion, drive consensus and facilitate decision-making to propel the document development cycle forward: Ensuring alignment with sponsor goals and project milestones while monitoring study progress. Fostering regular communication with subject matter experts (SMEs) to streamline document development (getting inputs timely, consolidating contributions or answering questions.) Manage client interaction Setting client expectations with document development Addressing feedback and confidently leading meetings with Big Pharma and Biotech clients WHO YOU ARE Bachelor's degree in biomedical, life sciences, or related discipline. Some medical writing experience within a CRO, Pharma, or Biotech is ideal. If you don't have medical writing experience, we still want to hear from you if you have strong scientific writing, data analysis and attention to detail gained from, i.e.: Recently completing your PhD, or Working in a fast-paced research lab, handling experimental data analysis and report writing. To succeed in this job, you´ll need visibility, proactivity and excellent communication skills. You should be comfortable with changing priorities and deadlines, managing complex regulatory documents, and confidently engaging with experts in their medical and statistical fields. WHY FORTREA? Diverse Career Path: Unique training schemes and opportunities to shape your career path. Supportive Environment: Comprehensive training, management support, and a network of SMEs to help you thrive. Career Growth: Whether you're passionate about scientific writing or aspire to leadership roles, your journey with us is driven by your aspirations. Join Fortrea and be part of a team that values your skills and supports your career growth. Where do you see yourself? Apply now and make an impact with Fortrea!

Learn more about our EEO & Accommodations request here.

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What You Should Know About Medical Writer I, Fortrea

Are you passionate about scientific writing and ready to make a real impact? Join Fortrea as our next Medical Writer I in Leeds! In this pivotal role, you'll be part of a dynamic team dedicated to ensuring that new medicines are safe for patients. Your contribution will be vital in developing essential clinical documents for early-phase clinical trials, especially in safety and pharmacokinetics. Fortrea, one of the largest Clinical Research Organizations globally, offers a cutting-edge facility in Leeds, designed to foster innovation and collaboration. As a Medical Writer I, you'll enjoy a hybrid work model, allowing for a blend of remote work and in-office training, perfect for those living in or around Leeds. You'll start your journey by learning the nitty-gritty of Medical Writing, which includes getting hands-on experience in designing Protocols and Clinical Study Reports (CSRs). With guidance from seasoned colleague, your role will also involve project management, collaborating with cross-functional teams, and ensuring clear communication with clients. To succeed, you'll need a Bachelor’s degree in biomedical, life sciences, or a related field, and some experience would be a plus. However, if you have strong scientific writing or data analysis skills, Fortrea wants to hear from you! With diverse career paths, a supportive environment, and real opportunities for growth, this is your chance to embark on an exciting journey at Fortrea. Apply today and start making a difference in clinical research!

Frequently Asked Questions (FAQs) for Medical Writer I Role at Fortrea
What are the responsibilities of a Medical Writer I at Fortrea?

As a Medical Writer I at Fortrea, your primary responsibilities include developing essential clinical documents such as Protocols and Clinical Study Reports (CSRs) for early-phase clinical trials. You'll play a vital role in analyzing clinical research data, particularly in safety and pharmacokinetics, and condensing complex information into clear, concise language. Project management is also key; you'll coordinate with cross-functional teams, facilitate discussions, and ensure alignment with sponsor goals and project milestones.

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What qualifications are needed for the Medical Writer I position at Fortrea?

To qualify for the Medical Writer I position at Fortrea, candidates should uphold a Bachelor's degree in biomedical, life sciences, or related disciplines. While some prior medical writing experience is ideal, candidates with strong scientific writing skills or relevant data analysis experience, particularly from completing a PhD or working in a research lab, are also invited to apply. Excellent communication skills, attention to detail, and the ability to manage complex regulatory documents are essential.

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What does the career growth look like for a Medical Writer I at Fortrea?

At Fortrea, career growth for Medical Writer I positions is encouraged through unique training schemes and mentorship. The company values versatility in career aspirations, whether you want to develop your expertise in scientific writing or aim for leadership roles. You'll have access to comprehensive training and support from management, allowing you to shape your career path as you grow with Fortrea.

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How does Fortrea support its Medical Writers in their roles?

Fortrea fosters a supportive environment for its Medical Writers through comprehensive training and mentorship by experienced colleagues. You'll work alongside a network of subject matter experts (SMEs), ensuring you have the resources you need to thrive. The goal is to nurture talent and provide ample opportunities for professional development, helping you succeed in your role and further your career.

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What is the work environment like for a Medical Writer I at Fortrea?

The work environment at Fortrea for a Medical Writer I is dynamic and collaborative, featuring a mix of remote and in-office work. The state-of-the-art facility in Leeds fosters teamwork and innovation, while also providing flexibility. You'll work in a fast-paced setting where fostering regular communication with stakeholders and subject matter experts is key to successfully driving document development and meeting project milestones.

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Common Interview Questions for Medical Writer I
What inspired you to pursue a career as a Medical Writer?

When answering this question, focus on how your passion for science and communication drives your interest in Medical Writing. Share specific experiences, such as relevant academic projects or roles in research, that highlight your commitment to conveying complex information clearly.

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How do you handle tight deadlines and shifting priorities?

In your response, emphasize your organizational skills and ability to remain calm under pressure. Share strategies you use for time management, such as prioritizing tasks and communicating with stakeholders to ensure timely deliverables.

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Can you describe your experience with clinical trial documents?

When discussing your experience, even if limited, focus on any relevant coursework or projects you’ve completed. Mention your familiarity with clinical writing formats and emphasize your strong attention to detail and understanding of the regulatory environment.

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How do you approach the analysis of clinical data?

Demonstrate your analytical skills by providing examples of how you've processed and interpreted data in the past. Speak about your methods for condensing information into concise summaries and your comfort with statistical or pharmacokinetic data if applicable.

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What is your writing process for developing clinical documents?

Outline your writing process, including how you gather information, collaborate with team members, and revise drafts. Highlight your commitment to clarity and precision while paying attention to the regulatory specifications for clinical documents.

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How do you ensure alignment with sponsor goals in document development?

Explain your strategies for maintaining regular communication with clients and gathering their feedback. Discuss your proactive approach in aligning documents with client specifications while ensuring adherence to project milestones.

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What tools and software are you proficient in for medical writing?

Be open about the writing tools and software you are experienced with, such as Microsoft Word, reference managers, or statistical analysis programs. If relevant, mention specific medical writing software that facilitates document preparation and formatting.

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Can you give an example of when you had to work with multiple stakeholders?

Provide an example that showcases your teamwork and communication skills. Highlight a project where you coordinated with diverse teams toward a common goal while managing various inputs and meeting deadlines.

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How do you stay current with industry regulations and guidelines?

Discuss your commitment to continuous learning and how you engage with professional resources, such as industry articles, webinars, or training sessions. Mention all the relevant organizations or publications you follow to remain knowledgeable.

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What do you find most challenging about medical writing, and how do you overcome it?

Share a specific challenge you’ve encountered in writing, such as understanding complex data or regulatory guidelines. Discuss the strategies you employed to address these challenges and emphasize your adaptability and solution-oriented mindset.

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Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and technology solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare i...

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Full-time, hybrid
DATE POSTED
April 17, 2025

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