Location: | London |
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Salary: | £34,841 |
Hours: | Full Time |
Contract Type: | Fixed-Term/Contract |
Placed On: | 29th May 2024 |
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Closes: | 10th June 2024 |
Job Ref: | 355262 |
The MHRA is transforming. Through enabling innovation, making the right judgements of the benefits and risks of medical products and forging the right partnerships in the UK and internationally, it aims to deliver world class regulation and improved outcomes for UK patients.
We are currently looking for a Clinical Study Manager to join our Clinical Practice Research Datalink team in the Safety and Surveillance group.
Within a week of working here, your day could look like this: you will be responsible for delivering projects using the CPRD online study platform and will include configuration and testing of study specific modules; collecting metrics and reporting on progress against key performance indicators; working with clients and colleagues across CPRD to deliver studies on time and to target in compliance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs).
The successful candidate will have a healthcare or life sciences degree or equivalent work experience. Have project management experience and experience in producing reports and study documentation. Have previous employment experience in a clinical research operations role.
Have experience in managing clinical research projects to a successful conclusion in line with UK clinical trials legislation and Good Clinical Practice (GCP).
Have excellent verbal and written communication skills including the ability to communicate in a clear, succinct and engaging manner.
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