**Job Title:** Document Processor II
About the Role:
* We are seeking an experienced document processor to join our team in a global role.
Key Responsibilities:
* Process, review, and resolve rejected trial master file (TMF) documents for complex studies or sponsor portfolios of studies in both electronic and hard copy formats.
* Perform periodic TMF quality control to ensure adherence to regulatory, ICH GCP, sponsor, and industry best practices.
* Work with various electronic document management systems to review, classify, and process essential documents.
* Communicate directly with the RMC lead to report trends and issues relevant to the TMF.
* Evaluate any TMF quality issues and escalate them in a timely manner to the RMC lead.
* Provide administrative support for the RMC lead, including filing and maintaining internal documents on study SharePoint.
Requirements:
* Proficiency in using an electronic document repository or eTMF, and document recognition skills.
* Strong interpersonal skills in a fast-paced, deadline-oriented environment.
* Sound judgment and ability to identify decisions requiring supervisory approval.
* Proficiency in Microsoft Word and Excel.
Your Background:
* University degree preferred (life science desirable).
* 1-2 years of relevant experience.
* Knowledge of working within a highly regulated industry (desirable).
What You Will Bring:
* The ability to work independently and as part of a team.
* A proactive approach to identifying and resolving issues.
* Excellent communication and organizational skills.
About You:
* You have excellent problem-solving skills and a keen eye for detail.
* You are able to prioritize tasks effectively and manage your time efficiently.
* You possess strong analytical and critical thinking skills.