Medical Writer I

Fortrea


Job Location:

Leeds - UK

Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

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.

Fortrea Clinical Pharmacology Services (CPS) supports the earliest and most critical phases of clinical development. Our teams work across project management clinical operations data biometrics laboratories and scientific functions to deliver earlyphase and complex multisite studies for global sponsors.

From firstinhuman studies to Phase 1B and exploratory programs CPS generates the safety tolerability PK and PD data that guide drug development decisions.

LOCATION

As one of the largest Clinical Research Organizations (CROs) in the world we have four Early Phase Clinical Research Units (CRU) in the UK and US and the jewel in the crown is our CRU at Drapers Yard Leeds. A brand new world class state-of-the-art 65000 ft² Phase I clinic only 7 minutes walking from the train station.

This is a full-time permanent job ideal for candidates living in the Yorkshire area as we offer a hybrid work model:

  • Initially 3 days office presence in Leeds for training and teamwork is needed. Rest of the week you could work remote.

WHAT YOU WILL DO

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.

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 youll 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

Youll 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

  • Bachelors degree in biomedical life sciences or related discipline.
  • Some medical writing experience within a CRO Pharma or Biotech is ideal.

If you dont 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 results report writing.

To succeed in this job youll 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 youre 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!

#LI-CV1 #Li-hybrid

Learn more about our EEO & Accommodations request here.

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.Fortrea Clinical Pharmacology Services (CPS) supports the earliest and most cri...

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