TMF Document Specialist I

Job Description

*Trial Master File (TMF) Document Specialist ICome discover what our 25,000+ employees already know: work here matters everywhere. We re a growing and evolving biopharmaceutical industry leader, which means you ll have endless opportunities to work with experts around the world and build the career you ve dreamed of. As a part of the Syneos Health team, you ll help us deliver results for a rewarding reason we improve patients lives around the world. Because to us, a patient isn t just a number, they re our family, friends, and neighbors.Why Syneos Health #SyneosHealthLife means we re committed to our Total Self culture where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person s unique contributions make a difference. We believe our success is a direct result of the people who are driving it you We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That s why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial. We are continuously building the company we all want to work for and our customers want to work with. Why Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives we re able to create a place where everyone feels like they belong.Job responsibilities Process study documentation in accordance with Standard Operating Procedures (SOPs), Work Instructions (WIs), GCP, ICH guidelines and study specific TMF Plans. Support the set-up, maintenance, and closure of TMF repositories. Support documentation collection activities, including: o Document scanning and indexing for trial using an electronic TMF o Document filing for trials using a paper TMF Perform quality review of documents submitted for entry into the TMF and liaise with project teams to resolve any issues identified Maintain compliance with departmental quality, performance and utilization targets Complete administrative tasks (e.g., status reports) as requested Maintain compliance with company requirements (e.g., time tracking, training) Participates in preparation/reconciliation of TMF documentation related to audits, inspections and shipments. Participates in study specific training as required. For Paper documents, responds promptly to each request received for a project document or project file, ensures timely and appropriate delivery to the requestor, and timely and accurate re-filing upon return. Ensures that all applicable paperwork is completed upon release and return of each project document and/or project file from the Document Control Room Ensures the security and compliance of all documents related to active and archived projects Performs other work-related duties as assigned. Occasional travel may be required (up to 10%)., *What we re looking for High school education, some college courses in the scientific/regulatory field preferred. Some experience in a clinical trials environment preferred. Some knowledge of applicable regulations and guidelines with respect to regulatory documents and familiarity with medical terminology preferred. Familiarity with electronic TMF system preferred. Strong verbal, written and organizational skills with a team-oriented approach. Ability to handle and prioritize multiple tasks to meet deadlines in a dynamic environment. Proficiency in Microsoft Office Suite and Adobe Acrobat.Get to know Syneos Health We are the only full-service biopharmaceutical solutions company in the world. That means we bring together the best clinical and commercial minds to create a better, smarter, faster way to get medicines into the hands of patients who need it most. Learn more about Syneos Health.Additional Information: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Keyskills :
documentationpowerpointqualitycustomer relations