Clinical Research Professional
1 day ago
At Fortrea, we are seeking a talented Clinical Research Professional to join our team. This role involves playing a key part in the development of essential clinical documents for early phase clinical trials (I-IIa), with a focus on safety and pharmacokinetics.
This is a full-time, permanent job, with a hybrid work model that combines remote work with regular office presence for training and teamwork. 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, with a brand new, world-class 65,000 ft2 Phase I clinic in Leeds.
The successful candidate will learn the science behind Medical Writing, developing documents that enable the conduct of a clinical trial and analyzing data to help sponsors decide the future of their molecule. With on-the-job training and guidance from colleagues and managers, you'll be able to drive the development of simple design protocols and clinical study reports (CSRs) with minimal supervision, navigating the fast-paced timeliness of the document development cycle.
Salary: $85,000 - $110,000 per year, depending on experience.
Responsibilities:
- Develop clinical documents for early phase clinical trials
- Analyze data to inform sponsor decisions
- Work collaboratively with cross-functional teams
Requirements:
- Bachelor's degree in biomedical, life sciences, or related discipline
- Some medical writing experience within a CRO, Pharma, or Biotech
We offer a supportive environment, comprehensive training, and opportunities for career growth. If you're passionate about scientific writing and eager to learn, apply now
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