Clinical Trials Associate
4 semanas atrás
Job Title: Sr Clinical Research Associate | ICON Strategic Solutions
About the Role: As a Clinical Research Associate at ICON Strategic Solutions, you will play a vital role in the success of our clinical trials. Your responsibilities will include onsite and remote monitoring activities, ensuring patient safety and data integrity.
Key Responsibilities:
- Monitoring Activities: Complete onsite and remote monitoring activities in accordance with ICH-GCP guidelines, applicable regulations, SOPs, and study processes.
- Study Participant Protection: Verify the protection of study participants by confirming informed consent procedures and protocol compliance with applicable regulations.
- Data Integrity: Ensure the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations, and SOPs.
- Reporting: Write and submit reports of investigational site findings and updates to applicable tracking systems.
- Issue Resolution: Escalate observed deficiencies, issues, and corrective and preventative action plans as appropriate.
- Audit Preparation: Participate in audit preparation and follow-up activities as needed.
- Training: May serve as a preceptor, providing training to less experienced clinical team members.
Requirements:
Qualifications: Bachelor's degree in a health, life sciences, or other relevant field of study. Previous experience supporting clinical trials, including solid onsite monitoring experience. Travel is required. All employees must read, write, and speak fluent English and host country language.
At ICON: We value diversity, inclusion, and belonging. Our diverse workforce makes us more innovative, enabling us to better serve our people, patients, customers, and communities. We're committed to providing an inclusive and accessible environment for all candidates.
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