Clinical Trials Document Manager
1 week ago
As a Regulatory Compliance Specialist at Worldwide Clinical Trials, you will play a key role in ensuring the accuracy and completeness of our clinical trial documents. This position requires attention to detail, organizational skills, and excellent communication abilities.
About Us:
Worldwide Clinical Trials is a global CRO with a strong reputation for delivering high-quality services to our clients. Our team members enjoy a dynamic and supportive work environment that fosters growth and development.
Key Responsibilities:
* Verify the accuracy and completeness of TMF documentation
* Collaborate with project teams to develop and implement procedures for maintaining accurate and compliant TMF records
* Perform periodic reviews of TMF documentation to ensure adherence to regulatory requirements
Requirements:
* 2+ years of experience in regulatory compliance or a related field
* Strong analytical and problem-solving skills
* Excellent communication and teamwork skills
Salary: $75,000 - $95,000 per year
Benefits:
* Comprehensive health insurance plan
* Retirement savings plan with company match
* Paid time off and holidays
What We Offer:
We offer a competitive salary, comprehensive benefits package, and opportunities for career advancement.
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