Clinical Operations Officer
at Protas
Sverige, , Sweden -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 08 Jul, 2024 | Not Specified | 09 Apr, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
EXCITING OPPORTUNITY FOR A FORWARD-THINKING INDIVIDUAL LOOKING TO MAKE BIG IMPACT ACROSS MULTI-INTERNATIONAL CLINICAL TRIALS HELPING.
About Protas
Protas is an independent not-for-profit organisation, designing and delivering large, global randomized clinical trials of treatments for common and other life-threatening diseases. Protas is led by the epidemiologist and physician, Professor Sir Martin Landray, who has over 20 years’ experience of leading large, randomized clinical trials as part of a team at Oxford University’s Nuffield Department of Population Health. Most recently, he has been co-leading the landmark RECOVERY clinical trial into treatments for COVID-19 which identified that treatment with the inexpensive steroid drug dexamethasone, improved the chances of survival for the most severe cases. It’s an incredibly rewarding place to work where you’ll be surrounded by supportive colleagues who are experts in their own field of excellence.
About the role
As clinical operations officer you will support the delivery of all operational aspects of Protas’ clinical trials, including setting up and maintaining trial sites for effective and efficient operation and managing the logistics of trial-related materials to and from the site. Preparing drafts of trial operations plans and working to agreed milestones ensuring high standards of quality in the execution of their duties
In this role you will build experience across all operational aspects of Protas’ trial portfolio, including process management, trial site set up and sample management. This is an ideal role for someone with some experience working in clinical trials who wants to develop their skills across a broad range of clinical ops functions.
About you
You have experience of working as part of a team supporting trial operations, logistics and supply chain management in a large scale, highly regulated environment, with the ability to work effectively as part of a multi-disciplinary international team. Planning and prioritisation comes naturally to you, and you have a good understanding of the principles of project management. Lastly, you ideally have experience of working in a healthcare or clinical trial setting.
ADDITIONAL INFORMATION
Protas is committed to being a diverse and inclusive organisation. We strongly encourage applications from people from all backgrounds. For disabled applicants, please contact us to let us know of any adjustments we can make to support you during the recruitment process.
We are currently a primarily remote working organisation but plan to move to hybrid working in the future. We welcome applications from locations across the UK (applicants must have the right to work in the UK).
Job Level: D - £41,200 per annum
Please note this role closes on: 19th April 2024
View Full Job Description and Role Requirement
How To Apply:
Incase you would like to apply to this job directly from the source, please click here
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Sverige, Sweden