Medical Writer I

Fortrea; Leeds; Hybrid; GBP 30,000 - 40,000; Full time

Job summary

A leading Clinical Research Organization is seeking a Medical Writer 1 in Leeds, UK. In this full-time role, you will develop essential clinical documents for trials, collaborating with cross-functional teams while receiving training. The ideal candidate has a biomedical degree and strong scientific writing skills.

Benefits

Unique training schemes

Comprehensive management support

Opportunities for career growth

Qualifications

• Bachelor's degree in biomedical, life sciences, or related discipline.
• Medical writing experience within CRO, Pharma, or Biotech is ideal.

Responsibilities

• Drive the development of design Protocols and Clinical Study Reports (CSRs) with minimal supervision.
• Critically review and interpret clinical research data (especially Pharmacokinetics and safety).
• Project Manage the document development cycle.

Skills

Scientific writing

Data analysis

Attention to detail

Excellent communication

Education

Bachelor's degree in biomedical or life sciences

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

This job is ideal for candidates living in or around Leeds.

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 in Leeds for training and teamwork.

WHAT YOU WILL DO

Learn the science behind Medical Writing and 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.

Ability to live and work in the UK (we cannot sponsor for this role)

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!

#LI-CV1 #LI-Hybrid

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