Sr. Clinical Scientist

ICON; São Paulo; Teletrabalho; BRL 150.000 - 200.000; Tempo integral

Resumo da oferta

A global healthcare company is seeking a Senior Clinical Scientist in Brazil to lead the design and execution of clinical studies. The role requires an advanced degree in a relevant field and extensive experience in clinical research. You will collaborate with cross-functional teams and analyze clinical data to support innovative treatments. This position offers competitive benefits and a supportive work environment.

Serviços

Various annual leave entitlements

Health insurance

Retirement planning offerings

Global Employee Assistance Programme

Flexible optional benefits

Qualificações

• Extensive experience in clinical research and study design, preferably in the pharmaceutical industry.
• Strong understanding of regulatory guidelines for clinical trials.
• Ability to analyze clinical data effectively.

Responsabilidades

• Lead clinical study design and execution, ensuring protocol adherence.
• Collaborate with teams to develop protocols and reports.
• Interpret clinical data to support regulatory submissions.
• Provide scientific input during clinical development.
• Establish partnerships with stakeholders for study alignment.

Conhecimentos

Strong communication

Analytical skills

Leadership

Data interpretation

Collaboration

Formação académica

Advanced degree in medicine or life sciences

Descrição da oferta de emprego

Sr. Clinical Scientist - Remote - Brazil

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Senior Clinical Scientist to join our diverse and dynamic team. As a Senior Clinical Scientist at ICON, you will play a pivotal role in designing and conducting clinical studies that evaluate the safety and efficacy of innovative treatments. You will contribute to the advancement of groundbreaking therapies through your expertise in clinical trial design, data analysis, and regulatory compliance.

What You Will Be Doing

• Leading the design and execution of clinical studies, ensuring adherence to protocol and regulatory requirements.
• Collaborating with cross-functional teams to develop study protocols, informed consent forms, and study reports.
• Analyzing clinical data and interpreting results to support decision-making and regulatory submissions.
• Providing scientific input and strategic guidance throughout the clinical development process.
• Establishing partnerships with key stakeholders to ensure alignment on study objectives and outcomes.

Your Profile

• Advanced degree in a relevant field such as medicine, life sciences, or pharmacology.
• Extensive experience in clinical research and study design, preferably within the pharmaceutical or biotechnology industry.
• Strong understanding of regulatory guidelines and requirements related to clinical trials.
• Excellent analytical skills and experience in statistical analysis and data interpretation.
• Strong communication, interpersonal, and leadership skills, with the ability to influence and drive results in a collaborative environment.

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

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please apply here