Senior CRA
On-siteCambridge, Massachusetts, United States or Cary, North Carolina, United States
Job Summary
Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conduct site visits to assess performance, resolve issues, and provide support for successful trial execution. Collaborate with cross-functional teams for accurate data collection and reporting while training site staff to maintain high clinical conduct standards. Build effective relationships with site personnel and stakeholders to facilitate smooth operations. This role requires approximately 60% travel and involves leading monitoring tasks with a focus on quality and continuous improvement within ICON's global clinical research organization.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously
- Strong organizational and problem-solving skills
- Expertise in monitoring practices
- Data integrity
- Site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication skills
- Interpersonal skills
- Stakeholder management skills
- Ability to influence and drive compliance within a complex environment
- Willingness to travel as required (approximately 60%)
- Legal right to work in the country where the role is based
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