Clinical Research Associate ll
- Recruiter
- RBW Consulting
- Location
- Camberley
- Salary
- Competitive
- Posted
- 07 Aug 2022
- Closes
- 23 Aug 2022
- Sectors
- Scientific & Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
Clinical Research Associate II
United Kingdom (Home Based)
GBP35,000 - GBP45,000
Finding a role which you truly enjoy is sometimes challenging, however, it is so important that we find the right role as we spend more time at work than we do at home.
Working in Clinical Research is an extremely rewarding career, as everyday you have the opportunity to really make a difference.
How would you like to work for a company who really value your input and the work you do along with handsomely rewarding you for your efforts.
Due to impressive growth plans, my client is looking for their next CRA superstar. You will be conducting national monitoring visits although an effort will be made to try and allocate sites close to where you live. You will have in-depth knowledge of the clinical trial process and always put the needs of the patient first.
Further duties will include:
Coordinating phase l - lV clinical trials
Performing the full suite of site visits: qualification, initiation, monitoring, motivational, audit support and close out
Identifying and conducting feasibility assessments for proposed study sites in accordance with the Project team
Liaising with other departments to ensure smooth running of the study
Reporting on serious adverse events
Checking drug accountability
Must Haves:
Life Science degree or similar
Driving License
Demonstrable SIV/IMV/COV experience
18 - 24 months within a CRA role
If you are interested in the above role, please send your CV to (mailto:) or call me on
United Kingdom (Home Based)
GBP35,000 - GBP45,000
Finding a role which you truly enjoy is sometimes challenging, however, it is so important that we find the right role as we spend more time at work than we do at home.
Working in Clinical Research is an extremely rewarding career, as everyday you have the opportunity to really make a difference.
How would you like to work for a company who really value your input and the work you do along with handsomely rewarding you for your efforts.
Due to impressive growth plans, my client is looking for their next CRA superstar. You will be conducting national monitoring visits although an effort will be made to try and allocate sites close to where you live. You will have in-depth knowledge of the clinical trial process and always put the needs of the patient first.
Further duties will include:
Coordinating phase l - lV clinical trials
Performing the full suite of site visits: qualification, initiation, monitoring, motivational, audit support and close out
Identifying and conducting feasibility assessments for proposed study sites in accordance with the Project team
Liaising with other departments to ensure smooth running of the study
Reporting on serious adverse events
Checking drug accountability
Must Haves:
Life Science degree or similar
Driving License
Demonstrable SIV/IMV/COV experience
18 - 24 months within a CRA role
If you are interested in the above role, please send your CV to (mailto:) or call me on