Contract Analyst I

ICON; São Paulo; Teletrabalho; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading company in clinical research, ICON, seeks a Contract Analyst to manage operations, budgets, and ensure compliance with regulatory guidelines. Ideal candidates will have extensive clinical research experience, strong leadership skills, and a BA/BS degree. Benefits include flexible scheduling, health insurance, and a commitment to wellness and diversity.

Serviços

Various annual leave entitlements

Health insurance options

Retirement planning options

Global Employee Assistance Programme

Flexible benefits (childcare vouchers, gym discounts)

Qualificações

• ≥2 years of experience in pharmaceutical drug development.
• More than 5 years in the clinical research industry.
• Fluent in English.

Responsabilidades

• Manage day-to-day operations ensuring compliance with GCP/ICH guidelines.
• Lead internal teams and manage functional budgets and resources.
• Provide accurate project status and escalate issues proactively.

Conhecimentos

Project Management

Leadership

Communication

Regulatory Knowledge

Formação académica

BA/BS degree

Descrição da oferta de emprego

As a Contract Analyst, you will join the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

• Manage and may lead the day-to-day operations within relevant support functions to ensure completion per established goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements. This includes effective communication and coordination with key business stakeholders (e.g., study teams) to support timely completion of both drug and non-drug program goals and objectives.
• Manage and may lead functional and cross-functional internal teams.
• Provide accurate and up-to-date project status and financial information within relevant tracking systems/tools.
• Proactively identify and escalate issues related to support functional deliverables.
• Implement standards for designated functional areas.
• Manage functional budgets and resources, oversee trial or support function budgets, timelines, and resources as appropriate.

You are:

• BA/BS degree with ≥2 years of experience in pharmaceutical drug development or equivalent.
• More than 5 years in the clinical research industry.
• Over 3 years of site contract & budget negotiation experience.
• Knowledge of clinical trial conduct, including multi-center, global trials.
• Strong knowledge of ICH/GCP guidelines and regulatory requirements.
• Proven project management and leadership skills.
• Excellent interpersonal, written, verbal communication, administrative skills, and computer literacy.
• Fluent in English.
• Full Home-Based role.

What ICON can offer you:

Our success depends on our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers a range of 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, and more.

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

At ICON, inclusion & belonging are central to our culture. We are committed to providing an accessible environment for all candidates and a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

https://careers.iconplc.com/reasonable-accommodations

If you're interested but unsure if you meet all requirements, we encourage you to apply. You might be exactly what we're looking for, whether for this or other roles.