Senior Clinical Research Associate

ICON Strategic Solutions; Town of Poland (NY); Vor Ort; USD 70.000 - 90.000; Vollzeit

Benefits dieser Stelle

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Zusammenfassung

ICON Strategic Solutions is seeking a Clinical Research Associate to lead on monitoring clinical trials, ensuring adherence to protocols and regulatory standards. You will conduct site visits, provide guidance to site staff, and collaborate across teams to facilitate successful trial execution.

This role requires a Bachelor's degree and extensive experience in clinical research. ICON offers a competitive salary and a comprehensive range of benefits designed for work-life balance and family well-being.

Qualifikationen

• Extensive experience as a Clinical Research Associate necessary.
• Proven ability to manage multiple sites and projects simultaneously.
• Willingness to travel approximately 60%.

Aufgaben

• Monitor clinical trial sites for adherence to protocols and regulations.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with teams for timely and accurate data collection.
• Provide training and support to site staff and CRAs.
• Build effective relationships with site personnel and stakeholders.

Kenntnisse

Clinical trial monitoring

Regulatory compliance

Organizational skills

Stakeholder management

Problem-solving skills

Communication skills

Ausbildung

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Tools

Clinical trial software

Jobbeschreibung

ICON plc is a world-leading healthcare intelligence and clinical research organization. We are 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.

What You Will Do

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Key Responsibilities

• 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

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

Required Qualifications And Experience

• 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%)

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

• 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 who are there to support you and your family’s well‑being.
• Life assurance
• Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion and belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply.