What are the responsibilities and job description for the Study Management Specialist position at Radiometer?
We are currently seeking a talented and experienced Senior Clinical Study Manager to join our Clinical Affairs department at Radiometer. This is an exciting opportunity to work on a wide range of clinical projects, collaborating with internal stakeholders and external partners to deliver high-quality results.
As a Senior Clinical Study Manager, you will be responsible for overseeing all aspects of clinical trials, including developing and implementing study protocols and monitoring plans, selecting clinical sites, driving timelines in coordination with the clinical monitoring team, and ensuring compliance with SOPs and regulatory requirements. You will also provide regular study progress communication and escalate issues as needed.
To be successful in this role, you will need to possess a strong understanding of clinical trial management principles and practices, as well as excellent communication and interpersonal skills. You will also need to demonstrate a commitment to quality and excellence, with a focus on delivering high-quality results in a timely and efficient manner.
The essential requirements of the job include:
- Bachelor's Degree in a relevant field with 9 years of experience, OR Master's Degree with 7 years of experience, OR Doctorate/PhD degree with 4 years of experience
- Knowledge and experience with Good Clinical Practices (GCP) and global IVD, medical device regulations
- Demonstrated agility with processes and details, ability to apply critically thinking, analyze data, and solve complex problems
- Strong work ethic, ability to work independently, and demonstrated ability to deliver assignments on time, and effectively communicate and escalate
- Proficiency in Microsoft Office applications (PowerPoint, Excel, Word)
