Freelance Clinical Research Associate at TFS HealthScience

Hamburg, , Germany -

Full Time

Start Date

Immediate

Expiry Date

08 Feb, 26

Salary

0.0

Posted On

10 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Monitoring, Data Integrity, ICH-GCP, SOPs, Regulatory Compliance, Communication, Organization, Time Management, Medical Terminology, Analytical Skills, Collaboration, Proactivity, Detail Orientation, Independent Work, Team Environment

Industry

Pharmaceutical Manufacturing

Description

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. About this role As a Clinical Research Associate, you will support the initiation, on-site and remote monitoring, and close-out of clinical trial sites, ensuring participant safety, data integrity, and compliance with ICH-GCP, SOPs, and regulatory requirements. Key Responsibilities: Monitor clinical trials on-site and remotely in line with TFS/sponsor SOPs, ICH-GCP, and regulations. Ensure subject safety, protocol adherence, informed consent compliance, and data accuracy. Review source documentation and CRFs and verify Investigational Product management. Document monitoring activities in timely, accurate reports and escalate issues when needed. Maintain ISF and deliver required documents to TMF/eTMF; update CTMS and project systems. Support audits, inspections, and clinical supply management (as applicable). Qualifications: Bachelor’s degree in life sciences, nursing, or equivalent; 1+ year of relevant clinical experience. Solid understanding of medical terminology, GCP, ICH guidelines, and regulatory requirements. Strong communication, organization, and time-management skills; tech-savvy and detail-oriented. Ability to work independently and collaboratively in a matrix team environment. Fluent in English; flexible, proactive, analytical, and collaborative mindset. What We Offer We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients A Bit More About Us Our journey began over 25 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East. Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization. #Together we make a difference

Responsibilities

As a Clinical Research Associate, you will support the initiation, on-site and remote monitoring, and close-out of clinical trial sites. You will ensure participant safety, data integrity, and compliance with ICH-GCP, SOPs, and regulatory requirements.