Medical Writer I
New Yesterday
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.
- 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
- Bachelor's degree in biomedical, life sciences, or related discipline.
- Some medical writing experience within a CRO, Pharma, or Biotech is ideal.
- Recently completing your PhD, or
- Working in a fast-paced research lab, handling experimental data analysis and report writing.
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.
Apply now and make an impact with Fortrea!
#LI-CV1 #LI-Hybrid
Learn more about our EEO & Accommodations request here. #J-18808-Ljbffr
- Location:
- Leeds, England, United Kingdom
- Salary:
- £80,000 - £100,000
- Job Type:
- FullTime
- Category:
- Bio & Pharmacology & Health
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