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Clinical Research Associate
5 days agoWhat's your preference?
Job Description
- Req#: 6Jsp1oHk0naf
Employer Industry: Contract Research Organization (CRO)
Why consider this job opportunity:
- Competitive compensation package and comprehensive benefits
- Opportunity for personal and professional growth in a rewarding environment
- Fully remote work flexibility, allowing you to work from anywhere
- Join a collaborative team dedicated to making a difference in patients' lives
- Focus on clearing a backlog of source data verification, enhancing your skills in clinical monitoring
What to Expect (Job Responsibilities):
- Conduct on-site and remote monitoring visits in compliance with SOPs, GCP, ICH, and regulatory requirements
- Ensure patient safety and protocol compliance by verifying informed consent and adherence to study guidelines
- Review case report forms (CRFs) and source documentation for completeness, accuracy, and overall data quality
- Oversee investigational product handling and accountability at clinical sites
- Prepare timely monitoring visit reports, issue lists, and follow-up actions while escalating issues as needed
What is Required (Qualifications):
- Bachelor’s degree in life science, nursing, or equivalent
- Minimum one year of relevant monitoring or clinical research experience
- Strong understanding of GCP, ICH, and general clinical research processes
- Excellent communication skills with the ability to build productive site relationships
- High level of organization, attention to detail, and ability to work independently
How to Stand Out (Preferred Qualifications):
- Proficiency in common software and clinical systems
#ContractResearch #ClinicalResearch #RemoteWork #CareerGrowth #PatientSafety
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