Clinical Research Site Monitor: Drive Quality Trials
IQVIA
A global clinical research organization is seeking a site monitor to ensure compliance with study protocols and regulatory requirements. The role involves visiting sites, tracking recruitment progress, and collaborating with study team members. Candidates should have at least 2 years of on-site monitoring experience and a Bachelor's Degree in a scientific discipline. Strong communication, organizational, and problem-solving skills are essential for effective project execution. #J-18808-Ljbffr
Vacancy posted 2 days ago
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