TMF Operations Associate Role
This role is responsible for the processing, maintenance and archiving of essential documents in compliance with regulatory requirements.
* Process and review rejected Trial Master File (TMF) documents in electronic and hard copy formats.
* Perform periodic quality control to ensure adherence to regulations and industry best practices.
* Review, classify and process Essential Documents using Electronic Document Management Systems.
* Communicate with team members to report trends and issues relevant to TMF.
* Educate others on TMF Quality Control procedures.
Key Responsibilities
1. Manage document repositories and maintain accurate records.
2. Develop and implement procedures for document processing and quality control.
3. Collaborate with stakeholders to resolve document-related issues.
4. Maintain up-to-date knowledge of industry best practices and regulatory requirements.
5. Ensure compliance with data management policies and procedures.
About You
* You will have a degree in a life science or related field.
* Relevant experience working in a regulated environment is desirable.
* You will possess strong analytical and problem-solving skills.
* Proficiency in Microsoft Word and Excel is required.
What We Offer
We are committed to providing opportunities for growth and development. If you are a detail-oriented individual with excellent communication skills, we encourage you to apply for this challenging role.