Medical Writer I

Fortrea; Leeds; Hybrid; GBP 30,000 - 50,000; Full time

Job description

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

1. 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, including critically reviewing and interpreting clinical research data (particularly Pharmacokinetics and safety), and condensing data and conclusions into clear concise language in Protocols and CSRs.

Project Manage the document development cycle: 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.

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?

1. Diverse Career Path: Unique training schemes and opportunities to shape your career path.
2. Supportive Environment: Comprehensive training, management support, and a network of SMEs to help you thrive.
3. 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!