January 22, 2018 – Clinical Research Document Specialist II – p b Job Description: /b /p ul li Generation, maintenance (including follow up for documents) and finalization of Trial Master File Table of
Position Roles & Responsibilities:
5 years of work experience is required, and Commercial Sponsorship Coordinator Specialist will be responsible for overseeing the compliant execution, process management and administration for the electronic approval system supporting Sponsorship and Exhibit requests.
Oversight for activities such as coordinating training, identifying and resolving systematic and process issues and concerns, partnering with key business stakeholders and the third party service provider(s) to enhance the system’s effectiveness and efficiency, monitoring transactions, document flow, approvals and exceptions and developing report
Serve as a key compliance resource for stakeholders across the commercial organization.
May 12, 2017 – Clinical Document Management Specialist IV – p b Job Description: /b /p ul li Reporting to the Clinical Documentation Team Lead, and working in collaboration with the clinical study teams,
April 7, 2017 – Clinical Document Management Specialist – p b Responsibilities: /b /p ul li Day to day monitoring of TMF-early planning and setup all the way to study closeout and performing of
Responsible to manage documentation associated with clinical trials, both in paper and electronic format, including transitions and conversions. To follow records management tasks, policies and procedures protecting record integrity by ensuring full compliance to GCP principles and client SOPs. “www.KatalystHLS.com”