Clinical Data Programmer Iii Sas

2 weeks ago

Bengaluru, India Novotech Asia Full time

Novotech is the Asia-Pacific CRO designed for biotech, accelerating clinical development via cutting-edge technology to improve patient lives.
Working in a fast-paced and adaptable environment, we strive to set the benchmark for both business and clinical trial performance across all clinical trial phases and therapeutic areas.
Our people are critical in meeting organizational, and client objectives and we place a strong emphasis on creating a collaborative, transparent, and inclusive work environment where everyone is supported to achieve.

**Responsibilities**:
1.Projects/Clinical Studies
- Participate in Client and Project meetings as required in consultation with the Team Lead CDP to explain the CDP requirements, process and through-put times.
- Undertake database configuration, programming of study database edit checks, custom functions, and clinical and operational progress reports.
- Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets.

2.Team

3.Software and Programming Tools
- Support in the validation of electronic systems, software and programs implemented in accordance with current regulatory requirements.
- Ensure proficiency with the company's programming languages and conventions used for designing electronic CRFs and edit checks and ensure proficiency with configuration of non-EDC systems used for data capture and reporting.

4.CDP Processes and SOPs
- Assist in the development and updating of SOPs and best practices, process improvement, quality control and governance related to all Clinical Data Programming matters.
- Adhere to applicable regulatory guidelines and Novotech' s corporate policies and procedures, and to SOPs, Forms, Libraries and Best Practice Programming conventions.

**Minimum Qualifications & Experience**:

- Graduate in information science or life science related field, or similar.
- More than three years' experience in a Clinical Data Programmer role in a pharmaceutical company, CRO or EDC software provider, including supervision and training of other programmers and familiar with programming languages including Java and C#.

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.

Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.

  • Clinical Data Programmer Iii Sas

    4 weeks ago

    Bengaluru, India Novotech Asia Full time

    **About the role**: The Clinical Data Programmer SAS III (must be SAS Certified) is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating...

  • Clinical Data Programmer Sas

    4 weeks ago

    Bengaluru, India Novotech Asia Full time

    **Brief Position Description**: The Clinical Data Programmer SAS is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating reports,...

  • Clinical Data Programmer Iii Sas

    4 weeks ago

    Bengaluru, India Novotech Asia Full time

    **Minimum Qualifications & Experience**: - Must be SAS Certified - Graduate in computer science, data science, mathematics, or life science related field, or similar. - A minimum of 5 years of experience in a role related to business intelligence, data science, data analysis, and clinical data management or clinical data programming in a pharmaceutical...

  • Clinical Data Programmer Iii Sas

    7 days ago

    Bengaluru, India Novotech Asia Full time

    **Minimum Qualifications & Experience**: - Graduate in computer science, data science, mathematics, or life science related field, or similar. - A minimum of 2 years of experience in a role related to business intelligence, data science, data analysis, and clinical data management or clinical data programming in a pharmaceutical company, CRO or EDC software...

  • Clinical Dm SAS Programmer

    4 weeks ago

    Bengaluru, Karnataka, India Novasyte Full time

    Good Clinical Domain knowledge with understanding of clinical phases and Work experience must be in clinical / healthcare domain. Experience in Clinical SAS Programming Experience in Data Import Programming using SAS, SAS Output Delivery system (ODS) for generating reports in specific output formats like RTF, PDF, and HTML. Handling missing values,...

  • Clinical Programmer

    4 weeks ago

    Bengaluru, Karnataka, India AstraZeneca Full time

    **Job Title: Clinical Programmer** **Career Level - C** **Skills required - **SAS, SQL, PowerBI, Python, MicroStrategy **Introduction to Role**: Are you ready to take a crucial inter-disciplinary approach to save patients' lives? As a Clinical Programmer, you will be primarily responsible for providing support to activities related to programming,...

  • Associate Clinical Data Programmer

    4 weeks ago

    Bengaluru, Karnataka, India Novo Nordisk Full time

    Associate Clinical Data Programmer **Category**:Data & AI**Location**:Bangalore, Karnataka, IN**Department**:Data Systems & Automation, Bangalore Global Development- **About the department** - Data Systems & Automation, Bangalore Global Development GBS is one of the most competent and diverse team of professionals who are mainly responsible for providing...

  • Clinical Data Programmer-edc

    3 weeks ago

    Bengaluru, India Novo Nordisk Full time

    **Department**:Data Systems & Automation, Clinical & Data Science (CDS) GBS** **About the department** Data Systems & Automation, Bangalore Global Development is one of the most competent and diverse team of professionals who are mainly responsible for providing functional and system support to execute clinical trials across Product Development Plan...

  • Sas Programmer

    4 weeks ago

    Bengaluru, India Fortrea - Organic Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Statistical Programmer III

    3 weeks ago

    Bengaluru, India Advarra Full time

    Principal Duties & ResponsibilitiesPerform, plan, co-ordinate and implement the following for complex studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and...

  • Project Clinical Data Programmer

    4 weeks ago

    Bengaluru, India Novo Nordisk Full time

    **Department**:Data Systems & Automation, Clinical & Data Science (CDS) GBS **About the department** Data Systems & Automation, Bangalore Global Development is one of the most competent and diverse team of professionals who are mainly responsible for providing functional and system support to execute clinical trials across Product Development Plan...

  • Statistical Programmer III

    4 weeks ago

    Bengaluru, India Advarra Full time

    Principal Duties & Responsibilities Perform, plan, co-ordinate and implement the following for complex studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal...

  • Statistical Programmer II

    3 weeks ago

    Bengaluru, India Lifelancer Full time

    Principal Duties ResponsibilitiesPerform and implement, under supervision,the following for clinical studies: (i) the SAS programming, testing, anddocumentation of statistical programs for use in creating statisticaltables, figures, listings, and graphs and (ii) the programming of analysisdatasets (derived datasets) and transfer filesfor internal and...

  • Statistical Programmer II

    3 weeks ago

    Bengaluru, India Advarra Full time

    Principal Duties & ResponsibilitiesPerform and implement, under supervision, the following for clinical studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal...

  • Statistical Programmer II

    4 weeks ago

    Bengaluru, India Advarra Full time

    Principal Duties & Responsibilities Perform and implement, under supervision, the following for clinical studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for...

  • Clinical Research Trainer

    4 weeks ago

    Bengaluru, India Airvin Skills Training and Consulting Pvt Ltd Full time

    **Responsibilities**: - Collaborate with cross-functional teams, including biostatisticians, data managers, and clinical research associates, to develop programming specifications and data analysis plans. - Design and develop SAS programs to generate tables, listings, and graphs (TLGs) for clinical study reports, regulatory submissions, and other...

  • Statistical Programmer Ii

    2 weeks ago

    Bengaluru, India Syneos Health Clinical Full time

    **Description** **Statistical Programmer II** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...

  • Statistical Programmer II

    4 weeks ago

    Bengaluru, India Lifelancer Full time

    Principal DutiesResponsibilitiesPerform and implement under supervision the following forclinical studies: (i) the SAS programming testing and documentationof statistical programs for use in creating statistical tablesfigures listings and graphs and (ii) the programming of analysisdatasets (derived datasets) and transfer filesfor internal andexternal clients...

  • Principal Stat Programmer

    4 weeks ago

    Bengaluru, India Syneos Health Clinical Full time

    **Description** **Principal Statistical Programmer** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to...

  • Data Facilitation Programmer

    7 days ago

    Bengaluru, India Novo Nordisk Full time

    **Department**:Data Analytics & Facilitation, Clinical & Data Science, Bangalore Global Development GBS **About the department** Data Systems & Automation (DSA), Data Management, Bengaluru is one of the most competent and diverse team of professionals who are mainly responsible for providing functional and system support to execute clinical trials across...