Lead Clinical Data Science Programmer

ICON Strategic Solutions; Brasil; Presencial; BRL 120.000 - 150.000; Tempo integral

Resumo da oferta

A leading clinical research organization is seeking a Lead Clinical Data Science Programmer to join their team. You will work with a large biotech company, focusing on Antibody research. The role involves translating reporting needs into specifications, developing standard reports, and collaborating with cross-functional teams. Ideal candidates will have a strong background in data management and programming, particularly in SQL and various reporting tools. ICON offers competitive salaries and a range of benefits to support work-life balance.

Serviços

Competitive salary

Work-life balance opportunities

Qualificações

• 5-8 years of data management experience in the pharmaceutical industry.
• Proficiency in SQL and scripting with experience in developing advanced queries.

Responsabilidades

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

Conhecimentos

Communication

Problem-Solving

Analytical

Formação académica

B.S degree in Biology, Computer Science, or equivalent

Ferramentas

SQL

JReview

Spotfire

SAS

Descrição da oferta de emprego

As a Lead Clinical Data Science Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

You will have the opportunity to gain experience working with a large biotech company, a pioneer and industry leader in the area of Antibody research, that utilizes their innovative technology platform across multiple therapeutics areas like Oncology, Infectious Disease, Cardiovascular and Metabolic Diseases.

What you will be doing:

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

EXPERIENCE

• B.S degree (Biology, Computer Science, programming, data management, scientific or analytic discipline or equivalent) with experience with programming and strong knowledge of database structures.
• 5-8 years of data management experience in the pharmaceutical industry
• 5 years of experience with various reporting and analytic tools - JReview, Spotfire, Tableau, Qlik, SAS, and SQL to include Integrated data, CRF data, eCOA and biomarker data
• All employees must read, write and speak fluent English and host country language.

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.

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

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, colour, 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 through the form below.

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

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.