Clinical Associate

ICON Strategic Solutions; Polska; Remote; PLN 120.000 - 180.000; Vollzeit

Benefits dieser Stelle

Annual leave

Health insurance

Retirement planning

LifeWorks EAP

Life assurance

Flexible benefits

Zusammenfassung

ICON Strategic Solutions Poland is seeking a Clinical Associate for a remote, sponsor-dedicated role. You will support clinical trial design, implementation and management, contributing to therapies benefiting patients worldwide.

Role requires coordinating trial activities, data collection and site management, with travel up to ~60% to sites. You will work with cross-functional teams to ensure data integrity and regulatory compliance in a remote Poland setting.

Qualifikationen

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• At least 2 years of experience in clinical research or healthcare (CTA).
• Experience with TMF and other Clinical Trials technologies.
• Strong organization, time management and data accuracy.
• Willingness to travel approximately 60%.

Aufgaben

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

Kenntnisse

Strong organizational skills

Attention to detail

Communication

Cross-functional collaboration

Ausbildung

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

Tools

TMF systems

Jobbeschreibung

Clinical Associate - Poland - Remote - Sponsor Dedicated

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 - at least 2 years as a CTA.
• Experience with TMF and other Clinical Trails’ technologies
• 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 (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 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, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.