Senior Clinical System Lead

ICON; Brasil; Presencial; USD 60.000 - 100.000; Tempo integral

Resumo da oferta

Join a pioneering firm in clinical research as a Senior Clinical System Lead. This role offers the chance to work with cutting-edge technologies in a diverse environment, focusing on data management and integrity across various therapeutic areas. You will engage with top-tier biotech companies, ensuring effective data usage and risk mitigation while contributing to innovative solutions in clinical data management. If you are passionate about data and eager to make a significant impact in the healthcare sector, this opportunity is perfect for you.

Serviços

Competitive Salary

Work-Life Balance Benefits

Diverse Culture

Well-being Programs

Qualificações

• 4+ years in clinical data management, ideally in BioPharma.
• Knowledge of modern data management platforms and technologies.

Responsabilidades

• Define and facilitate participant data journey and ingestion processes.
• Collaborate with technical and clinical teams to define data requirements.

Conhecimentos

Data Management

Analytical Skills

Clinical Data Management

Big Data Technologies

Risk Assessment

Formação académica

Bachelor's Degree in Computer Science

Bachelor's Degree in Data Science

Bachelor's Degree in Statistics

Ferramentas

EDC

Data Integration Tools

Descrição da oferta de emprego

As a Senior Clinical System Lead, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

You will have the opportunity to gain experience working with a large biotech company, a pioneer and industry leader in antibody research, utilizing their innovative technology platform across multiple therapeutic areas such as Oncology, Infectious Disease, Cardiovascular, and Metabolic Diseases.

What you will be doing

This role involves defining and facilitating the participant data journey, including identifying data sources, transport methods, ingestion processes into the client’s ecosystem, and mitigating potential challenges to ensure data understanding, consistency, and integrity. You will collaborate with technical and clinical teams to define data requirements, provide solutions, and serve as a subject matter expert in data management and statistics to facilitate effective data use and risk mitigation.

1. Provide technical and procedural guidance on data ingestion and clinical data custody, interfacing with CROs, vendors, and internal teams.
2. Identify participant data sources, document them, and create study data flow maps to illustrate the clinical data journey. Contribute to technical data specifications for data ingestion at the client.
3. Act as the primary contact for nonstandard data ingestion and define data demand with enablement teams, both internal and external.
4. Define and perform reconciliation of data ingestion against transfer specifications.
5. Conduct risk assessments for study-level participant data content and advise on risk mitigation strategies, ensuring proper data collection and educating study teams.
6. Support digital health technologies and eSource data, providing setup and technical support, and maintaining data integrity while contributing to long-term solutions.
7. Evaluate and define strategic vendors supporting data ingestion and quality, participating in assessments to understand capabilities and limitations.
8. Work with data enablement teams on data ingestion, harmonization, transformation, validation, and automation for the Clinical Data platform.
9. Contribute to internal process improvements, ensuring compliance with current technology and regulatory standards.
10. Ensure adherence to the data governance framework for participant data.

You are:

• Knowledgeable about modern data management platforms and technologies, including Big Data, Lakehouse, and data integration tools.
• Experienced with clinical data sets, EDC, and non-CRF data.
• Possess strong analytical skills to work with large, complex datasets, including research and clinical data.
• Have a minimum of 4 years’ experience in clinical data management and acquisition, preferably in BioPharma, with an ideal candidate having 7+ years.
• Hold a Bachelor’s degree in Computer Science, Data Science, Statistics, or a related field.

What ICON can offer you:

Our success depends on our people. We strive to build a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON offers various benefits focused on well-being and work-life balance for you and your family.

Learn more about working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are core to our culture. We are committed to providing an inclusive, accessible environment and a workplace free of discrimination and harassment. Qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. For accommodations during the application process, contact us through the provided form.

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

Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly who we’re looking for, whether for this or other roles at ICON.