TMF Associate

TFS HealthScience; Madrid; Presencial; EUR 35.000 - 50.000; Jornada completa

Descripción de la vacante

A global Contract Research Organization is seeking a Trial Master File Associate to manage the TMF and support the study team. The ideal candidate has at least 2 years of experience in the CRO or pharmaceutical industry with knowledge of GCP/ICH guidelines. Strong communication, organizational skills, and a Bachelor's degree in Health Science are preferred. This role offers competitive compensation and the chance for professional growth in a collaborative environment.

Servicios

Competitive compensation package

Comprehensive benefits

Opportunities for personal and professional growth

Formación

• At least 2 years of experience in CRO or Pharmaceutical Industry with proven TMF Management.
• Advance level of English.
• Knowledge of GCP/ICH guidelines.

Responsabilidades

• Organize, maintain, and oversee the Trial Master File (TMF).
• Provide TMF Monthly Reports.
• Act as contact person for study team.

Conocimientos

TMF Management

Communication Skills

Organizational Skills

Teamwork Ability

Document Management Software

Educación

Bachelor’s Degree in Health Science or Document Management

Herramientas

VEEVA

Descripción del empleo

TEMPORARY CONTRACT (WITH POSSIBILITY TO BE EXTENDED)

The role

The Trial Master File Associate (TMF Associate) will be part of our SRS Unit and will function operationally as a member of the Study Team with the responsibility to organize, maintain and oversee the Trial Master File (TMF) according to company policies, SOPs, Work Instructions, regulatory requirements, TMF Functional Lead and PM delegation.

Responsibilities

• Notify study team that TMF is created and ready for document upload for eTMF or submission to pTMF
• Develop TMF Plan
• Provide training on study specific TMF requirements, guidelines including TMF Plan
• Perform QC2 on documents and documents reconciliation
• Provide TMF Monthly Reports to PM, Line manager and Head of TMF Delivery
• Regularly check TMF metrics, follow up on detected issues, ensure acceptable level of metrics
• Ensure TMF processes timely implementation and execution
• Adjusting study specific TMF Index/EDL in the relevant files/ system as directed by the PM (Project Manager)
• Ensure valid forms and templates are implemented and maintained in the assigned projects
• Check status of duplicates, documents in error, size and path length (if applicable), follow up on necessary corrections accordingly
• Coordinate Monthly and Quarterly TMF Reconciliation by creating Action Plan and submitting relevant report on the status
• Ensure TMF AoR completion and monitoring TMF transfer/shipment to the Sponsor
• Ensure delivery of fully executed TMF AoR to TMF Functional lead
• Actively follow up that the study team is submitting documentation, EDL maintenance for eTMF in cooperation with study team, following the process described in The TMF Plan and that the TMF is always submission and inspection ready
• Act as contact person for study team to support on all TMF issues/inquiries independently
• Identify general areas with missing documentation and inconsistencies and follow up with the study team for resolution
• Actively taking part in Study Team meetings and updates on the TMF status
• Assist and attend activities associated to quality controls, audits and regulatory inspections in relation to the TMF
• Identify TMF quality issues and escaliorate to the CRM/PM/Director, TMF Functional lead and collaborate in the action plans development
• Resolve in cooperation with Study team all issue identified by Sponsor after TMF transfer
• Set up the Investigator Site File (ISF)
• Actively contribute to the organization and development of routines to enhance the work at TFS
• Develops and maintains an effective relationship with the study team

Qualifications

• At least 2 year of experience in CRO or Pharmaceutical Industry with proven TMF Management (VEEVA)
• Bachelor’s Degree in Health Science or Document Management or equivalent work experience is preferred
• Advance level of English
• Knowledge of GCP/ICH guidelines
• Good written and communication skills
• Good organizational and multi-tasking skills
• Good software and computer skills
• Able to work in a fast-paced environment with changing priorities
• Teamwork ability

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.

A Bit More About Us

Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.