TFS HealthScience

Clinical Research Associate

TFS HealthScience · Full Time · 3 hours ago

TFS HealthScience

🌎 Israel ⭐ 0-2 yrs exp 💼 Healthcare

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.

clinical-research communication documentation organization compliance

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Senior Clinical Research Associate

TFS HealthScience · Full Time · 3 hours ago

TFS HealthScience

🌎 Israel ⭐ 2-5 yrs exp 💼 Healthcare

The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of study sites to ensure subject safety and data integrity. They must maintain study documentation in accordance with GCP, ICH guidelines, and regulatory requirements while providing guidance to project teams.

clinical-research communication documentation organization mentoring compliance

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Study Start Up Lead

TFS HealthScience · Full Time · 5 days ago

TFS HealthScience

🌎 Australia ⭐ 5-10 yrs exp 💼 Others

The Study Start Up Lead coordinates all startup activities from project award to site activation, ensuring deliverables and timelines are met. They manage strategic startup aspects, mitigate risks, and oversee regulatory and contractual obligations in compliance with quality standards.

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Clinical Trial Manager - Freelance

TFS HealthScience · Full Time · 6 days ago

TFS HealthScience

🌎 United Kingdom ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Trial Manager oversees day-to-day trial operations to ensure studies are delivered on time, within budget, and in compliance with GCP standards. Key duties include supporting study start-up, monitoring enrollment, and ensuring audit readiness for a dedicated sponsor.

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Clinical Research Associate - Freelance

TFS HealthScience · Full Time · 6 days ago

TFS HealthScience

🌎 United Kingdom ⭐ 2-5 yrs exp 💼 Healthcare

The CRA is responsible for monitoring study sites to ensure patient safety, data quality, and compliance with regulatory requirements. Key tasks include performing site visits, reviewing source data, and maintaining essential study documentation.

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Project Management Associate

TFS HealthScience · Full Time · 8 days ago

TFS HealthScience

🌎 Poland ⭐ 2-5 yrs exp 💼 Product

The role supports the planning, coordination, and execution of clinical trials, focusing on system management and documentation. It serves as a central point of contact for study teams to ensure operational support and compliance with timelines.

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Senior Project Manager

TFS HealthScience · Full Time · 15 days ago

TFS HealthScience

🌎 Poland, Portugal, Spain, Sweden, United Kingdom, United States ⭐ 5-10 yrs exp 💼 Product

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.

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Director Business Development - Oncology

TFS HealthScience · Full Time · 16 days ago

TFS HealthScience

🌎 Germany ⭐ 10+ yrs exp 💼 Sales

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.

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Director Business Development - Oncology

TFS HealthScience · Full Time · 16 days ago

TFS HealthScience

🌎 Spain ⭐ 10+ yrs exp 💼 Sales

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.

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Senior Quality Manager

TFS HealthScience · Full Time · a month ago

TFS HealthScience

🌎 Poland, Spain ⭐ 5-10 yrs exp 💼 Others

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.

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Principal Quality Manager

TFS HealthScience · Full Time · a month ago

TFS HealthScience

🌎 Poland, Spain ⭐ 10+ yrs exp 💼 Teaching

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.

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Business Development Manager

TFS HealthScience · Full Time · a month ago

TFS HealthScience

🌎 France ⭐ 5-10 yrs exp 💼 Sales

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.

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Director / Senior Director, Project Delivery – Ophthalmology

TFS HealthScience · Full Time · 2 months ago

TFS HealthScience

🌎 Argentina ⭐ 10+ yrs exp 💼 Others

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.

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QA - Responsible Person (GDP)

TFS HealthScience · Full Time · 2 months ago

TFS HealthScience

🌎 Czech Republic ⭐ 2-5 yrs exp 💼 Others

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.

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