Here at Fortrea we are recruiting a junior Clinical Research Associate I to work within our multisponsor clinical team.
Key Responsibilities
- Conduct site monitoring activities including prestudy initiation routine monitoring and closeout visits.
- Ensure patient safety data integrity and protocol compliance through source data review and oversight of informed consent.
- Manage study sites in line with project plans ensuring audit readiness and timely issue resolution.
- Act as the main point of contact for sites vendors and internal teams including oversight of supplies and documentation.
- Prepare accurate monitoring reports and support study delivery through efficient planning and travel management.
Requirements
- Degree in life sciences nursing or a related health discipline or equivalent relevant experience.
- At least 6 months experience in clinical research (e.g. site management study coordination inhouse CRA).
- Basic knowledge of ICHGCP regulatory guidelines and the clinical trial process.
- Strong organisational skills attention to detail and ability to work effectively in a matrix environment.
- Fluency in English and Romanian; willingness to travel as required and a valid driving licence.
Learn more about our EEO & Accommodations request here.
Here at Fortrea we are recruiting a junior Clinical Research Associate I to work within our multisponsor clinical team.Key ResponsibilitiesConduct site monitoring activities including prestudy initiation routine monitoring and closeout visits.Ensure patient safety data integrity and protocol complia...
Here at Fortrea we are recruiting a junior Clinical Research Associate I to work within our multisponsor clinical team.
Key Responsibilities
- Conduct site monitoring activities including prestudy initiation routine monitoring and closeout visits.
- Ensure patient safety data integrity and protocol compliance through source data review and oversight of informed consent.
- Manage study sites in line with project plans ensuring audit readiness and timely issue resolution.
- Act as the main point of contact for sites vendors and internal teams including oversight of supplies and documentation.
- Prepare accurate monitoring reports and support study delivery through efficient planning and travel management.
Requirements
- Degree in life sciences nursing or a related health discipline or equivalent relevant experience.
- At least 6 months experience in clinical research (e.g. site management study coordination inhouse CRA).
- Basic knowledge of ICHGCP regulatory guidelines and the clinical trial process.
- Strong organisational skills attention to detail and ability to work effectively in a matrix environment.
- Fluency in English and Romanian; willingness to travel as required and a valid driving licence.
Learn more about our EEO & Accommodations request here.
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