Remote Clinical Research Job at ICON plc, Germany
Are you an experienced Clinical Research Associate (CRA) looking to work on innovative clinical trials in the ophthalmology field? The Remote Clinical Research Job at ICON plc Careers in Germany offers an exciting opportunity to oversee clinical trial sites, ensure regulatory compliance, and contribute to advancing medical research while working in a dynamic and globally recognized clinical research organization.
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies in developing innovative treatments. The company specializes in clinical development services that help bring new therapies to patients faster.
With a strong global presence, ICON focuses on improving healthcare outcomes by combining scientific expertise, data intelligence, and clinical trial management. The company fosters a collaborative and inclusive work culture while driving innovation in clinical research and drug development.
Job Details:
- Job Title: Clinical Research Associate (CRA) – Ophthalmology
- Location: Frankfurt, Germany
- Work Model: Remote / Clinical Monitoring
- Department: Clinical Monitoring
- Job Reference: JR141893
- Industry: Clinical Research / CRO
- Travel Requirement: Up to 60% travel (domestic and international)
Key Responsibilities:
- Monitor clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines in this Remote Clinical Research Job at ICON plc Careers.
- Conduct site visits to evaluate site performance and ensure smooth clinical trial execution.
- Collaborate with cross-functional teams to ensure accurate and timely data collection and reporting in this Clinical Research Job in Germany.
- Provide training and guidance to site staff and other CRAs to maintain high standards in clinical trial operations.
- Build and maintain strong relationships with investigators, site personnel, and stakeholders in this Clinical Research at ICON plc.
- Ensure participant safety and data integrity throughout the clinical study lifecycle as a Clinical Research Associate.
- Support issue resolution and ensure clinical trials progress on schedule.
Educational Requirements for this Job:
Applicants for this role should have:
- Advanced degree in Life Sciences, or other relevant healthcare or scientific disciplines
- Extensive experience as a Clinical Research Associate within the clinical trials environment.
Skills Required:
- Strong knowledge of clinical trial processes and regulatory requirements.
- Expertise in site monitoring, data integrity, and clinical trial management.
- Experience managing multiple clinical trial sites and projects simultaneously.
- Proficiency with clinical trial software and monitoring tools.
- Excellent communication and stakeholder management skills.
- Strong organisational and problem-solving abilities.
- Fluency in English and German.
- Ability to travel frequently for site monitoring visits.
- Ophthalmology clinical trial experience is required.
Benefits of the Clinical Research Job:
- Competitive salary and performance-based rewards.
- Comprehensive health insurance plans for employees and families.
- Flexible benefits depending on the country of employment.
- Global Employee Assistance Programme offering 24/7 well-being support.
- Retirement planning options to help maximize long-term savings.
- Life assurance and additional protection benefits.
- Work-life balance initiatives and generous annual leave policies.
- Access to wellness programs, gym discounts, childcare support, and travel subsidies.
- Opportunity to work within a global clinical research organization, shaping the future of clinical development.
