Clinical Monitoring Specialist
Há 5 dias
We are seeking a highly motivated Clinical Monitoring Specialist to join our team in Clinical Research. As a key member of our team, you will be responsible for ensuring the integrity and quality of clinical trials by conducting site monitoring responsibilities according to our Standard Operating Procedures (SOPs), ICH guidelines, and GCP.
Key Responsibilities:- Conduct site monitoring visits to ensure compliance with study protocols and procedures
- Verify informed consent procedures and protocol requirements
- Ensure data integrity through careful source document review and query generation
- Prepare and implement project plans related to clinical monitoring responsibilities
- Bachelor's degree in a related field or equivalent experience
- At least 2 years of clinical monitoring experience
- Thorough understanding of ICH GCP guidelines and local regulatory requirements
- Fluent in English, both written and verbal
$85,000 - $110,000 per year
Benefits:- Competitive salary and benefits package
- Opportunities for career growth and professional development
- A collaborative and dynamic work environment
We are a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.
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