TMF Associate

Budapest · Remote ok

About this role

Job Title: TMF Associate

 

Employment Type: Full time, Permanent

 

Job Reports To: Manager, TMF Operations

 

Department/Unit Name: TMF Operations

 

 

Job Summary:

Responsible for the management of the Trial Master File (TMF) content and associated processes during the study life cycle from study set up to transfer/archiving. Work in partnership with study teams during periodic file reviews and audits to address findings related to the TMF. Manage access and organization of the controlled electronic file repository, in line with the defined file structure and access management framework. Work proactively and successfully within a cross-functional team. Communicate and promote department and company goals and practices. Interact with stakeholders in a way that fosters a positive working atmosphere and encompasses a professional and helpful attitude. Time allocated may be adjusted based on need. 

 

Positions Available: 2; Note this position is cross-listed in multiple countries.

\nService Delivery
  • Serve as the primary TMF contact for assigned studies.
  • Ensure TMF is complete and “inspection ready” throughout study lifecycle and documents are filed contemporaneously.
  • Work with Team Lead to create study specific TMF management and oversight documents (e.g., File Index, Expected Document Lists and TMF Management Plan) in alignment with study.
  • Develop and maintain study-specific work instructions, as needed.
  • Utilize organization skills to maintain a quality control schedule and perform periodic inventories of study TMF to ensure completeness.
  • Review and communicate out-of-scope and/or incomplete documents to study teams; escalating as needed.
  • Reconcile expected document lists based on study events and milestones.
  • Prioritize and resolve TMF help desk tickets; may include triaging activities.
  • Provide study specific TMF training to internal and/or external stakeholders, as needed.
  • Process and review documents, following applicable scanning and best practices and best practices, and applying ALCOA principles appropriately.
  • File and retrieve TMF documents in a timely manner.
Department Support
  • Complete routine administrative tasks in a timely manner (e.g., timesheets, metrics).
  • Participate in discussions, decisions and sharing of knowledge in department meetings, periodic presentations, and smaller working groups.
  • Seek opportunities to assist in the development, implementation and maintenance of internal systems (e.g., databases used to manage records).
  • Provide mentorship and training to junior level staff.
  • Propose suggestions and work on the development and maintenance of department quality system documents to improve efficiencies.
Qualifications
  • The successful candidate will possess a college diploma/degree and 1-3 years of relative related experience or on going training. They will have an understanding of TMF organization, implementation, and archival including relevant regulations and guidance to assure quality and integrity of TMFs. Have the ability to incorporate the principles of ALCOA in relation to TMF oversight.  Utilize skills in time management and problem-solving.  Identify challenges and problems and take the initiative to identify solutions.  Demonstrated computer literacy, proven functional knowledge of Microsoft packages and potential to develop.
Working Conditions
  • - Home based, with the ability to go into office occasionally if needed. 
  • *Accommodations for persons with disabilities are available on request in respect of all aspects of the recruitment and selection lifecycle. Requests can be directed to [email protected]
Warning
  • PHISHING SCAM WARNING: Alimentiv is aware of the continued increase of phishing scams, leveraging various methods of attack via email, text, voice and social media. Please note that Alimentiv only uses company email addresses, which contain “@alimentiv.com”, to communicate with candidates via email. If you are contacted by someone about an open job at Alimentiv, please verify the domain of the sender’s email address and that they are asking you to apply on this website. If you believe you’ve been a victim of a phishing scam, please contact your local government cyber authority to report.
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Company at a glance

Industry-leading specialty GI contract research organization (CRO) transforming clinical trial outcomes and accelerating the development of life-changing therapies. We bring together deep GI expertise, advanced medical imaging solutions, clinical operation excellence and cutting-edge precision medicine/laboratory services.

With a global network of 5,000+ sites in >60 countries and growing, we expedite study activation and maximize patient enrollment, ensuring efficient and impactful clinical trials. Trusted by pharmaceutical and biotech partners, we support over 70% of all IBD compounds in development today – delivering customized end-to-end solutions to bring novel therapies to market.

As a full-service CRO, our offering is tailored to meet your specific clinical research needs:

  • Clinical Trial Services
  • Medical Monitoring
  • Medical Imaging Solutions
  • Medical Research & Development
  • Medical Writing
  • Precision Medicine/Biomarkers
  • Clinical Pharmacology
  • Histopathology via Specialty Lab, AcelaBio
  • Spatial Biology
  • Statistics
  • Real-World Evidence

Headquartered in London, Ontario, Alimentiv operates with globally across Canada, the US, Europe, Asia-Pacific, and Latin America.

Founded1986
Team Size501-1,000 employees
WorkspaceRemote ok
IndustryPharmaceutical Manufacturing
Location
London, Ontario, Canada
LinkedInLinkedIn

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