When our values align, there's no limit to what we can achieve.Job OverviewGood understanding of assisting and supporting Clinical Operations tasks / in-house works.Office based (Sydney).Will be hiring as Direct Contractor with a 1-year period of employment (12 months).During this period of the contract, may consider training for transition to the CRA or iCRA role (as demonstrated by performance in the COA tasks and training and depending on the business needs it could be more than 12 months when to be considered as a Trainee for CRA or iCRA).We are open to consider experienced SC, CRC candidates who are looking for CRA (on-site travelling role) or iCRA (Study Start-up Associate) career path.Please indicate in your CV which next career path you are interested in developing (CRA or iCRA).Project Trails Master FileTrack, scan, code, input metadata, and/or apply naming convention and send/file documents to the relevant study Trial Master File (TMF) as per the Trial Master File Plan.Filing and archiving paper wet-ink documents in the Central Files office location as per the Trial Master File plan.Photocopy, print, distribute, and retrieve documents as needed.Support in creating and reviewing Note to Files (NTF).Maintain basic quality check procedures to ensure accurate maintenance of documents.Review/update TMF country and site issues in 30 days.Review/update EDL (Essential Documents List).Review/update TMF milestones.Clear QC stops (if applicable).Missing Letter Support (e.g., FUP letter, confirmation letter, cover e-mails, etc.
).Follow up with sites regarding pending documents.Transfer of documents to sponsor TMF systems (if applicable).Vendor ManagementTrack and manage vendor communication related to site staff access to systems (e.g., EDC, IVRS) during activation.Follow up with sites.Study-specific completion training.Payment SupportReview if site payment funds are completed as per site contracts and follow up with the responsible team accordingly.SkillsStrong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.Maintain a basic knowledge and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations, and applicable PAREXEL procedures.Good oral and written communication skills to internal and external customers.Flexibility to perform multiple tasks and ability to prioritize these to achieve project timelines.High commitment to and performs consistently high-quality work.Effective problem-solving skills.Mentor and train less experienced staff as appropriate.Active participant as a process and/or platform Subject Matter Expert (SME) with minimal LM oversight.Demonstrate attitude, teamwork, proactiveness, and confidence.#J-18808-Ljbffr