Clinical Research Associate Role
Job Description
We are seeking an experienced Clinical Research Associate to join our team. The successful candidate will be responsible for monitoring clinical studies, identifying and selecting investigational sites, and ensuring compliance with study protocols and regulatory requirements.
The ideal candidate will have a strong background in clinical research, excellent communication skills, and the ability to work independently in a fast-paced environment.
Responsibilities
1. Monitor clinical studies to ensure compliance with study protocols and regulatory requirements.
2. Identify and select investigational sites for clinical studies.
3. Verify that research staff, facilities, and investigational products meet adequate qualifications and resources.
4. Responsible for the safety and proper conduct throughout the trial.
5. Verify that source data/documents and other trial records are accurate, complete, and maintained.
6. Report adverse events, concomitant medications, and intercurrent illnesses in accordance with the protocol on the CRFs.
Requirements
* Strong knowledge of ICH-GCP.
* Ability to review and evaluate clinical data.
* Computer literacy desirable.
* Professional use of the English language; both written and oral.
* Good oral and written communication skills.
* Bachelor degree, or local equivalent, in medicine, science or related discipline.
* Home-Based.
* +2 yrs SIT On-Site Monitoring Experience and have global oncology studies.
Benefits
We offer a competitive salary package, including annual leave entitlements, health insurance offerings, retirement planning opportunities, and flexible country-specific optional benefits.
About Us
We are a global company dedicated to providing high-quality clinical research services. Our team is passionate about delivering exceptional results and making a positive impact in the lives of patients.