Trial Programmer Specialist Ii

5 meses atrás


Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.

PPD’s data analytics programming group supports the centralized monitoring organization in delivering new approaches to risk surveillance and centralized statistical monitoring. We create the data reports, data visualization, tools, and utilities the centralized monitoring group uses to monitor and manage clinical study data to proactively identify risks in a clinical trial. These tools provide insight into things like:

- Data errors, deviations
- Trends, outliers
- Unusual variation (or lack of variation)
- Potential data manipulation, fraud
- Other systematic errors or data integrity issues.

As a data analytics programmer, you’ll be mapping data, creating custom reports, creating custom visualizations/dashboards, and creating other specialized tools and utilities used in centralized statistical and risk surveillance activities on assigned trials.

At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees.

**Summarized Purpose**:
Computer programming position working with and integrating data from a variety of internal and external systems. Provides programming support for some or all of the following activities: creation, validation and maintenance of programs and visualizations used for risk reviews, risk metrics reporting and issue/risk trending to support Risk Based and Centralized Monitoring. Assists with developing tools and techniques for improving process efficiencies within Data Analytics; including but not limited to: data integration automation, data retrieval automation, and report generation automation.

**Essential Functions**:

- Independently create, execute, maintain and validate programs used to transfer data across multiple systems, integrate data from a variety of sources and structures, generate summary data from a variety of sources, generate reports or integrate multiple databases.
- Independently create, execute, maintain, publish and validate visualizations used in support of Centralized Monitoring.
- As a contributing member, assist in creating tools, techniques and processes for automating Data Analytics tasks (data integration automation, data retrieval automation, data mapping automation and automated report generation.)
- Perform other programming tasks as necessary to support Data Analytics or other functional groups involved in Risk Based and Centralized Monitoring.
- Responsible for clearly documenting all work; managing assignments to meet timelines and delivering high quality.
- Demonstrate a good understanding of the role of the programmer in the overall process.
- Increase personal and peer knowledge base and professional skills in areas including programming, risk-based monitoring, centralized monitoring, data science/data analytics, technology and techniques, clinical trials, and the pharmaceutical industry.

**QUALIFICATIONS**

**Education and Experience**:

- BA/BS degree in data analytics, data science, information systems, computer science, biostatistics, mathematics or related field
- 2+ years of programming experience and 1 year of clinical research or related experience.
- Must have database management, SAS, R, Iron Python or SQL programming experience
- Basic knowledge understanding of data visualization software or tools (Spotfire, Tableu, or other)
- OR
- Equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills and abilities.

**Knowledge, Skills and Abilities**:

- Knowledge of one or more programming languages.
- Exposure to one or more data visualization software tools, methods or techniques and associated scripting language
- Exposure to Risk Based Monitoring or Centralized Monitoring concepts
- Knowledge of relational data base structure and experience working with complex data systems.
- Intermediate knowledge of SAS programming is desirable
- Experience demonstrating a strong attention to detail.
- Experience demonstrating leadership ability and ability to work on a multi-disciplinary project team.
- Excellent problem-solving skills.
- Excellent written and verbal communications skills.
- Ability to effectively organize and manage multiple assignments with challenging timelines.
- Ability to adapt and adjust to changing priorities.
- Positive attitude and the ability to work well with others.
- Demonstrated initiative and motivation.
- Ability to mentor Associate Programmer in nuances of programming and improvement.


  • Logistics Specialist Ii

    7 meses atrás


    Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Logistic Specialist II focused on the import process for clinical trials.

  • Programmer Analyst Ii

    5 meses atrás


    Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    **JOB DESCRIPTION** We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of...

  • Programmer Analyst Ii

    5 meses atrás


    Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    **JOB DESCRIPTION** We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of...


  • São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job DescriptionAs a Clinical Trials Analyst II at Thermo Fisher Scientific, you will have the opportunity to lead and support our clients in the execution of clinical trials logistics. Your role will be crucial in ensuring the success of our clients' projects. Responsibilities:Support both...


  • São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro

    Clinical Research Associate II Specialist at ICON plc is a world-leading healthcare intelligence and clinical research organization.We foster an inclusive environment driving innovation and excellence, and welcome you to contribute to our mission to shape the future of clinical development.We are seeking a Clinical Research Associate II Specialist to join...

  • Programmer Analyst Ii

    5 meses atrás


    Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Job Description **JOB DESCRIPTION** We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and...


  • Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    **Work Schedule** Other **Environmental Conditions** Office **Sr Programmer Analyst** **Purpose**: **Responsibilities include but are not limited to**: - Collaborates with PV business users to understand the requirements and recommend solutions. - Creates custom and ad-hoc reports from the PV Safety database using built in tools, OBIEE, or SQL. -...


  • São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Supporting Clients GloballyWe are seeking a skilled Clinical Trials Analyst II to join our team at Thermo Fisher Scientific. In this role, you will be responsible for providing logistical support to both foreign and local clients, understanding their specific requirements, and delivering tailored solutions.Key Responsibilities:Collaborate with clients to...


  • São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As a Clinical Trials Analyst II at Thermo Fisher Scientific Inc., you will have the unique opportunity to lead and support our clients in the flawless execution of logistics for clinical trials. Join our extraordinary team in São Paulo and play an important role in ensuring...


  • São Paulo, São Paulo, Brasil PSI CRO Tempo inteiro

    Job OverviewWe are seeking an experienced Site Network Development Specialist to join our Business Development team. This role is responsible for building and expanding the network of clients in the clinical trials industry.

  • Sas Programmer I

    4 semanas atrás


    São Paulo, São Paulo, Brasil Psi Cro Ag Tempo inteiro

    Job Title: Sas Programmer IAbout Us:Psi Cro Ag is a dynamic, global company founded in 1995, bringing together over 2,700 driven, dedicated, and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.Job Description:We are seeking a highly skilled Sas Programmer I to contribute...

  • Clinical Trial Manager II

    2 semanas atrás


    São Paulo, Brasil ENGINEERINGUK Tempo inteiro

    CTM II 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. At ICON, it's our people that set us apart. Our diverse teams enable us to become a...


  • São Paulo, São Paulo, Brasil Iqvia Tempo inteiro

    Job SummaryWe are seeking a skilled Clinical Trial Operations Specialist to join our team at Iqvia.About the RoleThe successful candidate will be responsible for the local management of clinical trials, ensuring compliance with Sponsor SOPs, WIs, policies, codes of Good Clinical Practice (GCP), and local regulatory requirements.Key ResponsibilitiesPrepare...


  • São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Lead Clinical Trials Logistics at Thermo Fisher ScientificAs a Clinical Trials Analyst II at Thermo Fisher Scientific, you will play a key role in ensuring the success of our clients' projects by leading and supporting the flawless execution of logistics for clinical trials.Responsibilities:Support clients by understanding their specific requirements and...


  • São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Lead Clinical Trials Logistics at Thermo Fisher ScientificAs a Clinical Trials Analyst II at Thermo Fisher Scientific, you will play a key role in ensuring the success of our clients' projects by leading and supporting the flawless execution of logistics for clinical trials.Key Responsibilities:Support clients by understanding their specific requirements and...


  • São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Supporting Clients GloballyWe are seeking a skilled Clinical Trials Analyst II to join our team at Thermo Fisher Scientific. As a key member of our global operations team, you will play a critical role in supporting both foreign and local clients by understanding their specific requirements and providing the best logistical solutions.Key...


  • São Paulo, São Paulo, Brasil Engineeringuk Tempo inteiro

    We are seeking a Clinical Trial Start-Up Specialist to advance clinical trial start-up activities by understanding client objectives and assisting in the development of the plan for country and site distribution.The ideal candidate will have a strong understanding of regulatory and submission processes in various countries and excellent written and verbal...

  • Data Analytics Programmer Ii

    2 semanas atrás


    São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    **Data Analytics Programmer Ii Role Overview**At Thermo Fisher Scientific, we are seeking a highly skilled Data Analytics Programmer Ii to join our team. This role will play a critical part in supporting our centralized monitoring organization.**Key Responsibilities:**Create and execute programs used to transfer data across multiple systems and integrate...


  • São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Job SummaryWe are seeking a highly skilled Clinical Trials Logistics Specialist to join our team at Thermo Fisher Scientific Inc. in São Paulo. As a key member of our team, you will be responsible for leading and supporting our clients in the execution of logistics for clinical trials.Key ResponsibilitiesSupport clients by understanding their specific...


  • São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As a Clinical Trials Analyst II at Thermo Fisher Scientific, you will have the opportunity to lead and support our clients in the execution of clinical trials logistics. Key responsibilities include supporting both foreign and domestic clients in the planning and execution of...