TFS HealthScience

Senior Clinical Data Manager

TFS HealthScience · Full Time · 10 days ago

TFS HealthScience

🌎 Spain ⭐ 10+ yrs exp 💼 Healthcare

Act as the Lead Clinical Data Manager responsible for preparing, conducting, and completing data management tasks across the full study lifecycle. This includes developing CRFs, managing databases, performing data cleaning, and coordinating with study teams and sponsors.

APPLY

Director Regulatory Affairs - Freelance

TFS HealthScience · Full Time · 10 days ago

TFS HealthScience

🌎 Denmark, Poland, Spain, Sweden, United Kingdom ⭐ 10+ yrs exp 💼 Legal

Provide expert scientific and regulatory guidance for an early phase drug reformulation project in ophthalmology. Define the overall regulatory and clinical development strategy and manage interactions with European regulatory authorities.

APPLY

Senior Clinical Research Associate

TFS HealthScience · Full Time · 22 days ago

TFS HealthScience

🌎 Sweden ⭐ 5-10 yrs exp 💼 Healthcare

The role involves independently planning and conducting site visits and overseeing study site performance for a global pharmaceutical or biotechnology sponsor. Responsibilities include reviewing eCRF data, maintaining study documentation, and collaborating cross-functionally to ensure inspection readiness.

APPLY

Director / Senior Director, Project Delivery – Ophthalmology

TFS HealthScience · Full Time · a month 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.

APPLY

QA - Responsible Person (GDP)

TFS HealthScience · Full Time · a month 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.

APPLY

Freelance Principal Database Programmer

TFS HealthScience · Full Time · a month ago

TFS HealthScience

🌎 Poland, United States ⭐ 10+ yrs exp 💼 Software Development

Lead the setup, validation, and programming of clinical study databases and ePRO/IRT systems. Provide mentoring to database programmers and manage project budgets and client deliverables within the Global Biometrics Department.

APPLY

Senior Clinical Research Associate - Medical Devices (Freelance)

TFS HealthScience · Full Time · a month ago

TFS HealthScience

🌎 Portugal ⭐ 5-10 yrs exp 💼 Healthcare

The Senior CRA is responsible for planning and conducting site visits, including initiation and close-out, for medical device studies in Portugal. They oversee site performance, manage study documentation, and collaborate with cross-functional teams to ensure regulatory compliance.

APPLY