The Trial Master File Associate is responsible for organizing, maintaining, and overseeing the Trial Master File (TMF) to ensure it remains inspection-ready throughout the clinical trial lifecycle. They will collaborate with study teams to manage documentation, perform quality control, and facilitate TMF reconciliation processes.
TFS HealthScience
9 Remote Job Openings at TFS HealthScience
The CRA is responsible for the initiation, monitoring, and close-out of clinical study sites to ensure subject safety and data integrity. This includes verifying protocol compliance, reviewing source documentation, and preparing timely monitoring reports.
Lead end-to-end delivery of cross-functional clinical projects, ensuring adherence to timelines, budgets, and quality standards. Act as the primary point of contact for global pharmaceutical or biotechnology clients while managing multidisciplinary teams.
Director Business Development - Oncology
TFS HealthScience
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Full Time
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a month ago
TFS HealthScience
The Director of Business Development is responsible for developing sales strategies and managing client retention within the Oncology sector in Germany. This includes identifying new business opportunities, leading the RFP/RFI process, and coordinating bid defense meetings.
Director Business Development - Oncology
TFS HealthScience
·
Full Time
·
a month ago
TFS HealthScience
The Director of Business Development is responsible for executing sales strategies and maintaining client retention within the Oncology sector. This includes identifying new business opportunities, managing the RFP process, and coordinating with internal teams to meet annual sales goals.
The Senior Quality Manager provides functional and project-level quality oversight to ensure compliance with GCP and GxP regulations. Responsibilities include managing eQMS activities, vendor quality assessments, and overseeing CAPAs and quality risk management.
The Principal Quality Manager serves as a subject matter expert and escalation lead for complex quality issues and inspection readiness. They oversee quality activities across projects and vendors while mentoring Quality Managers and improving the Quality Management System.
The Business Development Manager is responsible for driving sales strategy and client retention within the Oncology sector. This includes managing the RFI/RFP process, conducting bid defense meetings, and maintaining strong relationships with pharmaceutical and biotechnology clients.
Act as the QA Responsible Person for local batch release of medicinal products in the Czech Republic. Ensure compliance with GDP/GMP requirements and manage quality systems including deviations and CAPAs.