Senior Clinical Research Associate
ICON plc
full-time
Posted on:
Location Type: Hybrid
Location: Chicago • Illinois • United States
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Job Level
Tech Stack
About the role
- 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.
Requirements
- 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
Benefits
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Applicant Tracking System Keywords
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Hard Skills & Tools
clinical trial processesregulatory requirementsGood Clinical Practice (GCP)monitoring practicesdata integritysite managementproblem-solving
Soft Skills
organizational skillscommunication skillsinterpersonal skillsstakeholder managementinfluencing skills