Regulatory Compliance Specialist

1 month ago


Nottingham, Nottingham, United Kingdom Worldwide Clinical Trials Full time
Job Summary:
We are seeking a highly skilled Regulatory Compliance Specialist to join our team at Worldwide Clinical Trials. In this role, you will be responsible for ensuring the quality and compliance of clinical trial documents.

About Us:
Worldwide Clinical Trials is a global team of over 3,500 experts who are changing the way the world experiences CROs. We have a strong commitment to excellence and innovation in all aspects of our work.

Key Responsibilities:
* Fulfil the TMF Approver and/or TMF QC Reviewer roles as defined by Standard Operation Procedure(s) (SOP) and working practices
* Prepare periodic TMF Quality Control checklists for review by Project Team
* Perform periodic TMF Quality Control to ensure adherence to regulatory, ICH GCP, Sponsor, and industry best practices

Requirements:
* Data collection, indexing, and editing skills, including ability to adhere to standardized document naming conventions
* Proficiency in Microsoft Word and Excel

Salary: $70,000 - $90,000 per year

Benefits:
* Comprehensive health insurance plan
* Retirement savings plan with company match
* Paid time off and holidays

Why Work with Us:
We offer a dynamic and supportive work environment that allows our employees to grow professionally and personally. Our team members enjoy a range of benefits, including a competitive salary and comprehensive benefits package.

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