Clinical Research Associate

TFS HealthScience; Essen; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading global Contract Research Organization in Essen seeks a Clinical Research Associate to monitor clinical trial sites and ensure compliance with protocols and regulations. The ideal candidate will possess a Bachelor’s degree in life sciences, with over 5 years of experience in clinical research or monitoring. Excellent communication and organizational skills are required. This role offers a competitive compensation package and access to a supportive team dedicated to making a difference in patients' lives.

Leistungen

Competitive compensation package

Comprehensive benefits

Opportunities for personal and professional growth

Qualifikationen

• 5+ years of CRA or clinical research monitoring experience.
• Strong knowledge of ICH-GCP and regulatory requirements.
• Ability to travel as required and work independently.

Aufgaben

• Conduct site visits and prepare visit reports.
• Verify source data and ensure accurate data entry.
• Support site staff with study procedures and documentation.
• Identify, escalate, and help resolve study issues and risks.

Kenntnisse

Monitor clinical trial sites

Excellent communication

Organizational skills

Time-management skills

Ausbildung

Bachelor’s degree in life sciences 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.

a Clinical Research Associate.

About this role

As part of our FSP team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. This role is dedicated to one of our clients.

This role is a full-time role based Germany.

Key Responsibilities

• Monitor clinical trial sites to ensure protocol, GCP, and regulatory compliance
• Conduct site visits (initiation, monitoring, and close-out) and prepare visit reports
• Verify source data and ensure accurate, timely data entry
• Support site staff with study procedures and documentation
• Identify, escalate, and help resolve study issues and risks

Qualifications

• Bachelor’s degree in life sciences or a related field
• 5+ years of CRA or clinical research monitoring experience
• Strong knowledge of ICH-GCP and regulatory requirements
• Excellent communication, organizational, and time-management skills
• Ability to travel as required and work independently
• Experience working with women's health studies is a plus

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 30 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