Clinical Research Associate - Oncology Early Development - Central

ICON; Kansas City (MO); On-site; USD 60,000 - 100,000; Full time

Job summary

Join a forward-thinking clinical research organization committed to enhancing healthcare through innovative trials. In this role, you'll lead oncology early development projects, ensuring quality of life and effective patient recruitment. Collaborate with a diverse team, mentor junior members, and contribute to critical trial processes. Enjoy a supportive work environment that prioritizes your well-being and offers flexible benefits. If you're passionate about making a difference in clinical research, this opportunity is perfect for you.

Benefits

Health Insurance Options

Retirement Planning

Global Employee Assistance Programme

Life Assurance

Flexible Benefits

Gym Discounts

Childcare Vouchers

Travel Passes

Health Assessments

Various Annual Leave Entitlements

Qualifications

• 1.5-2 years’ experience in pharmaceutical clinical trial monitoring.
• Knowledge of GCP, ICH guidelines, and local regulations.

Responsibilities

• Work on multiple oncology early development trials.
• Mentor and coach junior team members.

Skills

Clinical Trial Monitoring

Oncology Trials

Patient Recruitment Strategies

Collaboration Skills

Communication Skills

Education

B.Sc. in Biological Sciences

R.N. (Registered Nurse)

Tools

CTMS

EDC

eTMF

IWRS

Job description

As a (job title), you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

What will you be doing?

• Work on multiple oncology early development trials
• Focus on quality of life with regional travel
• Demonstrate leadership through involvement in initiatives and serve as SME for systems and processes
• Mentor and coach junior team members
• Develop site start-up documents, including SIV agenda
• Provide input during review of study documents (e.g., Monitoring Guidelines)
• Represent LMTS or SMs in SMTs/meetings
• Review LTM reports (SQV, SMV, SCV) for assigned sites
• Support country budget development and contract negotiations with CCS colleagues
• Assist with ASV processes
• Adhere to Metrics/KPIs outlined in the QOP document

Interfaces – Primary/Other:

• Primary: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager, Central Study Team
• Others: Study Physician, Regional Quality & Compliance, Local Drug Safety Officer, Site Manager team, Investigators, and site personnel

Qualifications Needed:

• Based in Central US region, near a major airport
• Minimum of a B.Sc., R.N., or equivalent in Biological Sciences
• 1.5-2 years’ experience in pharmaceutical clinical trial monitoring
• 1-3 years’ experience in Oncology Early Development trials
• Experience with Oncology Phase I and II trials required
• Risk-based monitoring experience is a plus
• Ability to drive patient recruitment strategies
• Strong collaboration skills with investigators and site staff
• Proficiency with systems like CTMS, EDC, eTMF, IWRS, safety reporting
• Excellent communication and influencing skills; ability to work independently and remotely
• Deep knowledge of GCP, ICH guidelines, and local regulations
• Willingness to travel up to 40%
• Legally authorized to work in the US without future sponsorship requirements

What ICON can offer you:

Our success depends on our people. We prioritize diversity, high performance, and talent development.

In addition to a competitive salary, ICON offers benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements
• Health insurance options
• Retirement planning
• Global Employee Assistance Programme
• Life assurance
• Flexible benefits like childcare vouchers, gym discounts, travel passes, health assessments, etc.

Visit our website to learn more: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are core to our culture. We are committed to providing an accessible environment and equal opportunity employment. If you require accommodations during the application process, please contact us via the provided link.

Interested but unsure if you meet all requirements? We encourage you to apply—your skills may be exactly what we need.