At a Glance
- Tasks: Coordinate clinical pharmacology studies and manage essential project tasks.
- Company: Fortrea, a leader in clinical research with a focus on innovation.
- Benefits: Competitive salary, professional development, and supportive team environment.
- Other info: Join a dynamic team in Leeds with opportunities for career advancement.
- Why this job: Make a real difference in healthcare by managing impactful clinical trials.
- Qualifications: Degree in healthcare or science and strong communication skills.
The predicted salary is between 29700 - 36300 £ per year.
Fortrea is seeking a Clinical Project Coordinator in the United Kingdom (Leeds) to drive essential clinical pharmacology initiatives.
You will coordinate tasks for low to medium complex studies, initiate and maintain study documents, and support training of junior staff.
The role emphasizes precise project management, documentation control, and active liaison with external sites.
Candidates should have a healthcare/science degree and strong English communication.
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Pharmacology Clinical Project Coordinator – UK Trials in Leeds employer: FTLEE Fortrea Clinical Research Unit Ltd
FTLEE Fortrea Clinical Research Unit Ltd is an exceptional employer located in Leeds, offering a dynamic work culture that prioritises employee growth and development. With competitive compensation packages and a strong emphasis on compliance and support, employees are empowered to make a meaningful impact while advancing their careers in a collaborative environment.
Contact Details:
FTLEE Fortrea Clinical Research Unit Ltd Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Pharmacology Clinical Project Coordinator – UK Trials in Leeds
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We think you need these skills to ace Pharmacology Clinical Project Coordinator – UK Trials in Leeds
Some tips for your application 🫡
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at FTLEE Fortrea Clinical Research Unit Ltd that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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