Clinical Associate

ICON Strategic Solutions; United States; On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Retirement planning options

Employee assistance programme

Job summary

ICON Strategic Solutions is seeking a Clinical Associate in the United States to support the design, implementation, and management of clinical trials. You will contribute to coordination activities and deliverables, working with cross-functional teams to ensure quality data collection and regulatory compliance.

The role emphasizes collaboration with Clinical Operations, Data Management, and Biometrics, with opportunities for growth in a sponsor-dedicated environment that supports development of

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Experience in clinical research or healthcare, preferably in pharmaceutical/biotech/CRO.
• Strong organizational and time-management skills with ability to prioritise.
• Excellent attention to detail and problem-solving with data accuracy.
• Effective communication and cross-functional collaboration abilities.

Responsibilities

• Assist in planning, execution, and monitoring of clinical trials with protocol and regulatory compliance.
• Coordinate study activities including site initiation, patient recruitment, data collection and monitoring visits.
• Collaborate with Clinical Operations, Data Management, and Biometrics to support trial execution.
• Maintain study documentation and records in compliance with regulations and SOPs.
• Support study close-out activities including data cleaning, analysis, and study reports.

Skills

Clinical coordination

Regulatory knowledge

Attention to detail

Communication

Willingness to travel

Education

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

Job description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

What You Will Do

You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.

Key Responsibilities Include

• Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
• Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation.
• Collaborate with cross-functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials.
• Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures.
• Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports.

Your Profile

You will bring relevant clinical coordination experience, along with the following qualifications and skills.

Required Qualifications And Experience

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
• Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively.
• Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance.
• Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites.
• Willingness to travel as required

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 Examples Include

• 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.

At ICON, inclusion & 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