Clinical Research Associate

ICON Strategic Solutions; Pennsylvania; On-site; USD 65,000 - 95,000; Full time

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate – Oncology to monitor trials across OH, PA and VA, ensuring patient safety, data integrity and protocol compliance. You will conduct site qualification, initiation, monitoring and close-out visits and collaborate with investigators to drive study success.

The role requires oncology monitoring experience, ICH-GCP knowledge, and travel up to 60-75% within the Northeast region. A scientific or healthcare-related degree is required.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• Oncology monitoring experience required.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Skills

Attention to detail

Organizational skills

Communication skills

Independent and collaborative work

Travel readiness up to 60-75%

Education

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

Job description

Clinical Research Associate - Oncology - OH/PA/VA

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.

What You Will Do

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

Key Responsibilities Include

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.


• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.


• Collaborating with investigators and site staff to facilitate smooth study conduct.


• Performing data review and resolution of queries to maintain high-quality clinical data.


• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile

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

Required Qualifications And Experience

• Bachelor's degree in a scientific or healthcare-related field.


• Minimum of 2 years of experience as a Clinical Research Associate.


• Oncology monitoring experience required


• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.


• Strong organizational and communication skills, with attention to detail.


• Ability to work independently and collaboratively in a fast-paced environment.


• Willingness to travel as required up to 60-75% within their region (Northeast)

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.

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

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