Clinical Research Job at ICON – CRA Role in Germany | Apply Now
ICON is offering an exciting clinical research job for experienced professionals looking to grow their careers in global healthcare jobs. This clinical research job in Germany is ideal for Clinical Research Associates with strong regulatory knowledge, hands-on monitoring experience, and an interest in advancing innovative therapies through ICON careers.
Job Details:
- Job Position: Clinical Research Associate II
- Location: North-West Germany (North Germany region)
About the Company:
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. ICON careers are built around inclusion, belonging, and excellence, making this clinical research job a strong opportunity for professionals seeking long-term growth in global healthcare jobs.
Qualifications:
- Bachelor’s degree in a 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
- Fluency in English and German language
- Ability to work independently and collaboratively in a fast-paced environment
- Ability to travel at least 60% of the time (international and domestic – fly and drive), and should possess a valid driver’s license
Job Description:
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. This clinical research job is sponsor-dedicated and part of the Functional Service Provider (FSP) model in North Germany. As a Clinical Research Associate II 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 across healthcare jobs in Germany.
Key Responsibilities:
- 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
What ICON Can Offer You:
Our success depends on the quality of our people. That’s why ICON careers focus on building a diverse culture that rewards high performance and nurtures talent across healthcare jobs globally. In addition to your competitive salary, ICON offers a range of additional benefits designed to support well-being and work-life balance:
- Various annual leave entitlements
- A range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme (LifeWorks)
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and health assessments
