The Trial Master File Associate is responsible for organizing, maintaining, and overseeing the Trial Master File according to regulatory requirements and company SOPs. Key duties include developing TMF plans, performing quality control, and ensuring the TMF is inspection-ready.
TFS HealthScience
8 Remote Job Openings at TFS HealthScience
Clinical Research Associate - Freelance
TFS HealthScience
·
Full Time
·
6 days ago
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 informed consent, reviewing source documentation, and managing investigational products according to SOPs and GCP guidelines.
Manage the development and delivery of scientific and medical assets by coordinating workflows between internal stakeholders and external agencies. Establish process guidelines, track timelines, and monitor budgets to ensure efficient asset creation.
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.
Director / Senior Director, Project Delivery – Ophthalmology
TFS HealthScience
·
Full Time
·
2 months ago
TFS HealthScience
Establish and scale ophthalmology clinical operations across Latin America, providing end-to-end oversight of Phase I-III clinical trials. Lead regional delivery, build high-performing teams, and manage relationships with investigators and regulatory bodies.
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.