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About the Role
Oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Responsibilities
- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
- Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
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%).
- Must have the legal right to work in the country where the role is based.
Skills
- Clinical trial monitoring
- Protocol adherence
- Regulatory requirements
- Good Clinical Practice (GCP)
- Site management
- Data collection
- Data reporting
- Training
- Stakeholder management
- Clinical trial software
- Clinical trial tools
Location
- NorthEast
Work Type
- Full-time
Experience Level
- Senior
- Extensive experience as a Clinical Research Associate
Education Level
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
Salary/Compensations
- $110,520.00-$138,150.00
Benefits
- Competitive base salary
- Performance related incentives
- Health and wellbeing programmes
- Medical coverage
- Dental coverage
- Vision coverage
- Retirement plans
- Pension plans
- Life assurance
- Disability coverage
- Employee assistance programmes
- Wellbeing resources
- Learning and development opportunities
- Structured training
- Career pathways
About the Company
- ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
- As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
- ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide.
- You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live.
Equal Opportunity
- ICON is an equal opportunity employer.
- We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
- If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.