Clinical Site Manager II
Location
Texas
Posted
8 hours ago
Salary
0
Seniority
Senior
Job Description
Clinical Site Manager II
ICON plc
• You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement • 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
Job Requirements
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- 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
- Willingness to travel as required (approximately 60%)
Benefits
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
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