As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

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!

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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