Lead Clinical Data Science Programmer

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

Resumo da oferta

Join a leading clinical research organization as a Lead Clinical Data Science Programmer. This role offers the chance to work with a renowned biotech company, leveraging innovative technology in areas like Oncology and Infectious Disease. You will be responsible for translating reporting needs into actionable data solutions, collaborating with cross-functional teams, and ensuring compliance with regulatory standards. This dynamic position is perfect for those with a strong background in data management and a passion for improving healthcare outcomes. Enjoy a competitive salary and a supportive work environment focused on well-being and work-life balance.

Serviços

Competitive salary

Work-life balance benefits

Diverse culture

Talent nurturing programs

Qualificações

• 5-8 years of data management experience in the pharmaceutical industry.
• Experience with reporting and analytics tools like JReview, SpotFire, and SQL.

Responsabilidades

• Translate clinical study teams' reporting needs into specifications.
• Develop, test, deploy, and maintain global standard data review reports.

Conhecimentos

SQL

Scripting

Analytical Skills

Problem-Solving Skills

Communication Skills

Organizational Skills

Formação académica

B.S. degree in Biology, Computer Science, or related field

Ferramentas

JReview

SpotFire

SAS

Tableau

Qlik

Descrição da oferta de emprego

As a Lead Clinical Data Science Programmer, 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:

1. Translate clinical study teams' reporting needs into specifications and provide custom data review report solutions, including:
   1. Standard programs for patient profiles
   2. Reconciliation programs
   3. Standard and ad-hoc reports for data review to support clinical teams
   4. Develop, test, deploy, and maintain global standard data review reports on platforms like JReview, SpotFire, SAS, etc., including Integrated data, CRF data, eCOA, and biomarker data
   5. Update metadata definitions and specifications in an MDR system
   6. Collaborate with training teams to deliver custom role-based training to end users
   7. Generate reports for end users and multitask based on business needs
   8. Contribute to SOPs, Working Procedures, and internal documents
   9. Provide innovative solutions to generate metrics reports meeting business requirements
   10. Create compliance reports to confirm standards compliance
2. End-to-end knowledge of the drug development process
3. Understanding of FDA/ICH guidelines for clinical study data
4. Ability to collaborate effectively in a dynamic environment with cross-functional stakeholders such as scientists, operational leads, study physicians, data managers, and external data providers
5. Strong organizational and communication skills in a matrix environment, with attention to detail and a focus on high-quality results
6. Knowledge of regulatory guidelines for computerized systems in clinical trials
7. Strong analytical and problem-solving skills
8. Proficiency in SQL and scripting, with experience in developing advanced queries, stored procedures, and views. Experience with JReview, SpotFire, and SAS is a plus.
9. Working knowledge of drug development, FDA & ICC/GCP regulations
10. Experience with EDC build (Rave) is a plus

Experience:

1. B.S. degree in Biology, Computer Science, programming, data management, scientific or analytic discipline, or equivalent, with experience in programming and database structures.
2. 5-8 years of data management experience in the pharmaceutical industry
3. At least 5 years of experience with reporting and analytics tools such as JReview, Spotfire, Tableau, Qlik, SAS, and SQL, covering various data types including Integrated data, CRF data, eCOA, and biomarkers
4. Fluent in English and host country language

What ICON can offer you:

Our success depends on the quality of our people. We prioritize building 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 fundamental. We are committed to providing an inclusive, accessible environment free of discrimination and harassment. Qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. For accommodations, please visit https://careers.iconplc.com/reasonable-accommodations.

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