TFS HealthScience

Director, Regulatory Affairs EU

Director Regulatory Affairs

Lead European and global regulatory strategies; EMA/national authority experience; advanced life sciences degree; regulatory leadership.

Study Coordinator

Minimum 2 years clinical research or healthcare experience; study coordination/ nurselike role; good GCP and regulatory knowledge; English and MS Office proficiency.

Senior Clinical Research Associate

Degree in scientific/medical field or related training; CRA certification; several years of CRA experience; strong GCP/ICH knowledge; fluent German and English; willingness to travel.

Contract Manager

Bachelor’s degree in life sciences, law, finance, or related field; strong knowledge of ICH-GCP and local regulations; experience in clinical study management; detail-oriented; cell therapy experience; able to work from Hamburg or Munich 3 days/week.

Title	Location	Date
Director, Regulatory Affairs EU Contract Barcelona, Catalonia, Spain · Remote	Barcelona, Catalonia, Spain Remote	Mar 24, 2026
Study Coordinator Full Time · 2+ YOE Rome, Lazio, Italy · Hybrid	Rome, Lazio, Italy Hybrid	Mar 23, 2026
Senior Clinical Research Associate Full Time Frankfurt or Germany · Hybrid	Frankfurt or Germany Hybrid	Mar 23, 2026
Contract Manager Full Time Hamburg or Berlin or Frankfurt or Munich or Mainz · Hybrid	Hamburg or Berlin or Frankfurt or Munich or Mainz Hybrid	Jan 13, 2026

Name	TFS HealthScience
Headquarters	SE
Industries	Clinical ResearchPharmaceuticals
Activities	Clinical trial managementRegulatory affairs consultingBiostatistics and data managementMedical writing servicesSite selection and monitoring
Type	Private
Employees	700
Parent Company	Ratos AB
Tagline	Global Contract Research Organization providing clinical development and resourcing services.
Founded	1,996
Website	tfscro.com

TFS HealthScience

About TFS HealthScience