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Clinical Research Associate
4 months ago
Responsibilities
- Support CRAs with the setup monitoring and closeout of clinicaltrials in accordance with Good Clinical Practice (GCP) ICHguidelines and company SOPs.
- Assist in sitequalification initiation and monitoringvisits.
- Review and track clinical trialdocumentation ensuring accuracy andcompleteness.
- Collaborate with crossfunctionalteams to address studyrelatedissues.
- Participate in team meetings andcontribute to process improvementinitiatives.
Qualifications
- Currently enrolled in a relevant degree program such as listrelevant majors e.g. Life Sciences Biology Nursing PublicHealth
- Strong interest in clinical researchand drug development.
- Excellent organizationaland time management skills.
- Detailoriented withhigh standards for accuracy.
- Ability to workindependently as well as within a teamenvironment.
- Proficient in Microsoft OfficeSuite.
What YoullGain
- Realworld exposureto the clinical research process.
- Mentoringand guidance from experienced CRAs.
- Opportunityto network with industry professionals.
- Potential academic credit (if applicable with yourprogram).
- Potential for future employmentopportunities within ourcompany.
Please use the below linkfor job application and quickerresponse.
RemoteWork :
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