CRA II - Sponsor dedicated

ICON plc; Deutschland; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

ICON plc, a leading clinical research organization, is seeking a Clinical Research Associate II Specialist to join their dynamic team in Germany. The role involves overseeing clinical trials, ensuring compliance, and maintaining high-quality data. Candidates should possess a Bachelor's degree in a relevant field and at least two years of experience. ICON offers a competitive salary and diverse benefits focused on work-life balance and employee well-being.

Leistungen

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Qualifikationen

• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Excellent communication skills in German and English.

Aufgaben

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.

Kenntnisse

Organizational skills

Communication skills

Attention to detail

Ability to work independently

Ausbildung

Bachelor's degree in a scientific or healthcare-related field

Jobbeschreibung

CRA II/Senior CRA - sponsor dedicated

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Your profile

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Excellent communication skills in German and English.

What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements
• A range of health insurance offerings for you and your family
• Competitive retirement planning options
• Global Employee Assistance Programme, TELUS Health, providing 24-hour support
• Life assurance
• Flexible country-specific benefits like childcare vouchers, bike schemes, gym discounts, travel passes, health assessments, and more.

Visit our careers site to learn more about ICON's benefits.

At ICON, inclusion & belonging are fundamental. We are committed to providing an inclusive, accessible environment free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

If you need a reasonable accommodation during the application process or to perform essential job functions, please let us know or submit a request here.

If you're interested but unsure if you meet all requirements, we encourage you to apply. You might be exactly what we're looking for, whether for this role or others.

If you're a current ICON employee, please click here to apply.