Clinical Research Associate - Future Opportunities
About the role
We are proactively building a talent pool of experienced Clinical Research Associates (CRAs) to support future business growth within our Clinical Operations team.
Responsibilities
- Site selection, qualification, initiation, monitoring and close-out visits
- Clinical trial monitoring in accordance with ICH-GCP and regulatory requirements
- Site management and investigator relationships
- Source data verification (SDV) and quality oversight
- Risk-based monitoring approaches
- Protocol and regulatory compliance
- Clinical trial documentation and Trial Master File (TMF) management
- Site training and support
- Cross-functional collaboration with Project Management, Data Management and Regulatory teams
Requirements
- A Bachelor's degree in Life Sciences, Pharmacy or a related scientific discipline
- Experience working within a CRO environment
- Previous Clinical Research Associate (CRA) experience
- Strong understanding of ICH-GCP and clinical research regulations
- Willingness and ability to travel as required
Qualifications
- Full right to work in the country of employment
- Fluent English communication skills
Benefits
This opportunity is part of a Talent Pool initiative and is not an active vacancy at this time. However, we are interested in connecting with professionals who would like to be considered for future opportunities within our Clinical Operations team.
Pay
The pay range for this role is not specified at this time.
Schedule
The schedule for this role is not specified at this time.
Skills
Not specified at this time.
Benefits
Not specified at this time.
Pay
The pay range for this role is not specified at this time.
Schedule
The schedule for this role is not specified at this time.
Skills
Not specified at this time.
Benefits
Not specified at this time.
Application
To apply for this position, please visit the page hosted by JazzHR.