Clinical Research Associate

TFS HealthScience; Deutschland; Remote; EUR 45.000 - 60.000; Vollzeit

Zusammenfassung

A global Contract Research Organization is seeking a Clinical Research Associate to lead on-site and remote monitoring of clinical trials, ensuring compliance and patient safety. The ideal candidate will have a degree in life sciences, at least one year of experience, strong communication skills, and the ability to travel extensively. This role offers a competitive compensation package and opportunities for growth.

Leistungen

Competitive compensation package

Comprehensive benefits

Opportunity for growth

Qualifikationen

• At least one year of clinical research experience or relevant academic background.
• Clear and professional communication skills.
• Confidence using digital tools and systems.
• Willingness to travel up to 60-80%.

Aufgaben

• Lead on-site and remote monitoring of clinical trials.
• Champion participant protection by verifying informed consent.
• Review clinical documentation for accuracy and completeness.
• Capture insights and escalate issues as needed.
• Collaborate with sites to resolve findings.

Kenntnisse

Clinical research experience

Strong understanding of GCP and ICH guidelines

Communication skills

Organizational abilities

Fluency in English

Proactive mindset

Ausbildung

Degree in life sciences, nursing, or related field

Jobbeschreibung

Overview

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.

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.

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