Clinical Research Associate

TFS HealthScience; Hamburg; Vor Ort; EUR 45.000 - 60.000; Vollzeit

Zusammenfassung

A leading global CRO in Hamburg is seeking a Clinical Research Associate to ensure compliance during clinical trials. The role includes monitoring sites, verifying participant safety, and maintaining accurate documentation. Candidates should have a degree in life sciences and at least one year of clinical research experience. A proactive mindset and flexibility to travel up to 60–80% are required. Competitive compensation and opportunities for growth are offered.

Leistungen

Competitive compensation package

Comprehensive benefits

Personal and professional growth opportunities

Qualifikationen

• At least one year of clinical research experience or relevant academic background.
• Strong understanding of GCP, ICH guidelines, and basic medical terminology.
• Flexibility and willingness to travel up to 60–80%.

Aufgaben

• Lead on-site and remote monitoring of clinical trials.
• Champion participant protection by verifying consent procedures.
• Dive into clinical documentation reviewing CRFs and source data.

Kenntnisse

Good Clinical Practice (GCP)

Clinical research experience

Clear communication skills

Organizational abilities

Fluency in English

Ausbildung

Degree in life sciences, nursing, or related field

Jobbeschreibung

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 part of our Strategic Resourcing Solutions (SRS) team, you’ll be working alongside passionate and innovative professionals who are dedicated to delivering excellence in clinical research. Together, we help our customers bring life-changing therapies to patients around the world.

The Clinical Research Associate (CRA) is responsible for initiating, monitoring (on-site and remote), and closing out study sites during clinical trials, ensuring compliance with regulatory standards and safeguarding patient safety and data integrity.

Key Responsibilities:

• Lead on-site and remote monitoring of clinical trials, ensuring every visit supports data integrity, patient safety, and regulatory excellence.
• Champion participant protection by verifying informed consent procedures and protocol compliance.
• Dive into clinical documentation reviewing CRFs and source data to ensure accuracy and completeness.
• Oversee the management and accountability of investigational products, keeping everything audit-ready.
• Capture insights from monitoring visits in detailed reports, escalate issues when needed, and keep tracking systems up to date.
• Collaborate with sites to resolve findings, deliver action plans, and maintain top-tier documentation in the Trial Master File (TMF).

Qualifications:

• A degree in life sciences, nursing, or a related field.
• At least one year of clinical research experience or relevant academic background.
• Strong understanding of Good Clinical Practice (GCP), ICH guidelines, and basic medical terminology.
• Clear and professional communication skills, with excellent organizational abilities and attention to detail.
• Fluency in English and confidence using digital tools and systems.
• Flexibility, a proactive mindset, and willingness to travel up to 60–80%.

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