Clinical Research Associate - Oncology Early Development - Central (Field Based)

ICON; Brasil; Teletrabalho; BRL 20.000 - 80.000; Tempo integral

Resumo da oferta

A leading clinical research organization is seeking a clinical trial manager to oversee oncology early development trials. The role involves mentoring junior staff, ensuring quality oversight, and collaborating with various stakeholders. Candidates should have experience in oncology trials and a relevant degree. ICON offers competitive salaries and benefits focused on well-being and work-life balance.

Serviços

Various annual leave entitlements

Health insurance options

Retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible benefits like childcare vouchers

Qualificações

• 1.5 – 2 years’ experience in monitoring pharmaceutical industry clinical trials.
• 1-3 years’ experience in monitoring Oncology Early Development trials.
• Deep knowledge of GCP, ICH guidelines, and local regulations.

Responsabilidades

• Work on multiple oncology early development trials.
• Mentor and coach junior flex team members.
• Support country budget development and contract negotiations.

Conhecimentos

Collaboration

Analytical skills

Communication

Formação académica

B.Sc, R.N., or equivalent degree in Biological Sciences

Ferramentas

CTMS

EDC

eTMF

IWRS

Descrição da oferta de emprego

As a (job title), you will be joining 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 flex team members
• Develop site start-up documents, including SIV agendas
• Provide the SM “voice” when reviewing study documents (e.g., Monitoring Guidelines)
• Represent LTMs or SMs on SMTs/meetings
• Take over LTM role for reports review (SQV, SMV, SCV) for sites assigned to other SMs in the same trial
• Support country budget development and contract negotiations with CCS colleagues
• Assist with ASV processes
• Adhere to Metrics/KPIs outlined in the Quality Oversight Plan (QOP)

Interfaces – Primary/Other:

• Primary: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager, Central Study Team
• Other: Study Responsible Physician, Regional Quality & Compliance Manager/Specialist, Local Drug Safety Officer, Site Manager team, Investigators and delegates

Qualifications Needed:

• Located near a major airport in the Central US region
• Minimum of a B.Sc, R.N., or equivalent degree, preferably in Biological Sciences
• 1.5 – 2 years’ experience in monitoring pharmaceutical industry clinical trials
• 1-3 years’ experience in monitoring Oncology Early Development trials
• Experience with Oncology Phase I and II trials required
• Analytical/risk-based monitoring experience is a plus
• Ability to drive patient recruitment strategies
• Strong collaboration skills with investigators and site staff to meet study timelines
• Proficiency with systems like CTMS, EDC, eTMF, dashboards, IWRS, safety reporting
• Excellent communication and influencing skills for remote and face-to-face management
• 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

What ICON can offer you:

We prioritize building a diverse culture that rewards high performance and nurtures talent. Besides a competitive salary, ICON offers benefits focused on well-being and work-life balance, including:

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

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

ICON values inclusion & belonging. We are committed to an inclusive, accessible environment and equal opportunity employment. If you need accommodations during the application process, please inform us via this form.

Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly what we’re looking for!