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Senior CRA (Sponsor dedicated)

Frankfurt am Main, Hessen💼 Full-time🗓 2026-02-17 → 2026-07-25

Core

Overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards while ensuring data integrity and participant safety.

Role type

Senior Clinical Research Associate (Sponsor dedicated)

Builds

Clinical trials for healthcare clients

Domain

Clinical research / Life sciences

Deliverable

physical/clinical work

Required skills

Clinical trial process management, regulatory compliance, site monitoring, data integrity, project management, clinical trial software proficiency

Preferred skills

Advanced degree in life sciences, nursing, or medicine, ability to manage multiple sites simultaneously, problem-solving

Technologies

Clinical trial software and tools

Responsibilities

Monitoring clinical trial sites for protocol and GCP adherence, conducting site visits to assess performance and resolve issues, collaborating with cross-functional teams for data collection, providing training and guidance to site staff, building relationships with site personnel and stakeholders

Seniority

Senior, hands-on IC

Rewrite
## About the role Senior CRA 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 Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. ## What You Will Be Doing - Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. - Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. - Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. - Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. - Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. ## Your Profile - Advanced degree in a relevant field such as life sciences, nursing, or medicine. - Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. - Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. - Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. - Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. - Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license ## 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 additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals.
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