Senior Clinical Data Science Programmer
Há 2 dias
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 Data Science Programmer to join our diverse and dynamic team. As a Senior Clinical Data Science Programmer at ICON, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. You will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your programming expertise.
What You Will Be Doing:
- Develop, validate, and maintain programming solutions for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials.
- Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure the integration of programming solutions into the overall data management process.
- Act as a primary point of contact during the study set up and maintenance phase for system programming related questions by the project team.
- Support colleagues with the clinical trials environment and concepts of Clinical Data Management Systems.
- Perform extracts of data from CDMS and creation of data transfer programs.
- Act as mentor and provides guidance and support to more junior programmer levels assigned to a project.
- Assist in the development and implementation of improvements to technical systems and processes within an SME role.
- Provide guidance on programming best practices, coding standards, and data quality control measures.
- Stay updated on advancements in programming languages and data management tools to enhance operational efficiencies.
Your Profile:
- Complete bachelor's degree relevant field such as computer science, SAS, statistics, or life sciences.
- Extensive experience in programming for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials with proficiency in languages such as SAS, R, or Python.
- Strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment.
- Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results.
- Strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes.
- MUST HAVE advanced English Communication, Writing and Reading
#LI-Remote
#LI-FB2
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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised 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 click here to apply
-
Clinical Data Team Lead
Há 5 dias
São Paulo, São Paulo, Brasil IQVIA Tempo inteiro R$90.000 - R$120.000 por anoEssential FunctionsManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction.Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet...
-
Senior Clinical Lead
2 semanas atrás
São Paulo, São Paulo, Brasil IQVIA Tempo inteiro R$80.000 - R$120.000 por anoJob OverviewThe Sr. Clinical Lead provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project's overall objectives to the Sponsor's satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs,...
-
Clinical Data Reviewer
2 semanas atrás
São Paulo, São Paulo, Brasil PSI CRO Tempo inteiro R$40.000 - R$60.000 por anoCompany Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to...
-
Clinical Lead
1 dia atrás
São Paulo, São Paulo, Brasil IQVIA Tempo inteiro R$120.000 - R$240.000 por anoJob OverviewThe Clinical Lead provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project's overall objectives to the Sponsor's satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs, policies...
-
Data Science Senior Analyst
Há 3 dias
São Paulo, São Paulo, Brasil Dell Technologies Tempo inteiro R$40.000 - R$60.000 por anoData Science Senior AnalystA equipe de AI Innovation and Engineering do Brasil é uma parte dinâmica e desafiadora da Chief AI Office da Dell Technologies. Nós lideramos a pesquisa e a inovação para o futuro da Dell Technologies em um ambiente de alta visibilidade e alta colaboração. Trabalhamos de forma estreita com uma equipe global de cientistas...
-
Clinical Trials Assistant
1 dia atrás
São Paulo, São Paulo, Brasil IQVIA Tempo inteiro R$24.600 - R$46.120 por anoThis is a talent pool for people with disabilities. If you do not belong to this group and wish to apply, you can apply for other vacancies within IQVIA jobs.Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File...
-
Clinical Research Coordinator
1 semana atrás
São Paulo, São Paulo, Brasil IQVIA Tempo inteiro R$40.000 - R$60.000 por anoAre you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking Clinical Research Coordinator.This role has an immediate start working 24 hours a week for a...
-
Data Analytics Consultant
2 semanas atrás
São Paulo, São Paulo, Brasil Making Science Tempo inteiro R$40.000 - R$60.000 por anoAbout Making ScienceMaking Science is an international digital acceleration company with over 1,200 experts across 15 markets, including Spain, Portugal, Mexico, Colombia, France, Italy, the UK, Ireland, Sweden, Denmark, Norway, Finland, Germany, Georgia, and the USA. As a proud consulting partner of Local Planet — the world's premier network of...
-
Principal Clinical Research Associate
2 semanas atrás
São Paulo, São Paulo, Brasil CTI Clinical Trial and Consulting Tempo inteiro R$120.000 - R$240.000 por anoPrincipal Clinical Research AssociatePlease submit your CV in English for Quickest Review ProcessMaintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or milestone that...
-
Principal Clinical Research Associate
1 dia atrás
São Paulo, São Paulo, Brasil Cti Clinical Trial And Consulting Tempo inteiro R$120.000 - R$180.000 por anoPrincipal Clinical Research Associate Please submit your CV in English for Quickest Review Process Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or milestone...