Clinical Programmer Ii
2 days ago
**Job Title: Clinical Programmer II**
**Career Level - C**
**Introduction to role**
Are you ready to be part of a team that turns drug development strategies into reality? As a Clinical Programmer II, you will support programming, dashboard development, and validation of data cleaning and review listings for ongoing clinical studies with medium to high complexity. You will contribute to cross-functional initiatives and work under the guidance of an experienced programmer.
**Accountabilities**
- Independently program with efficiency and quality to support clinical study teams.
- Contribute to medium to high complexity projects within the clinical programming roadmap.
- Collaborate with data management, development operations, clinical, biometrics, and other relevant teams to deliver end-user reporting needs.
- Develop and maintain data visualization tools, including requirements gathering, design, data provisioning, building dashboards, leading validation/testing activities, and providing training.
- Create and maintain a catalogue of reports to aid data cleaning activities.
- Automate manual checks and reconciliation processes to ensure data quality.
- Create tools and repositories to minimize data errors at the source.
- Program operational reports and create visualizations to identify discrepancies in EDC and TPV data.
- Maintain and update the created catalogue of reports based on ongoing changes to requirements.
- Ensure availability and performance of developed reports and dashboards for both external and internal users.
- Complete documentation associated with programming tasks in compliance with applicable SOPs.
- Keep lead programmers updated on progress.
- Contribute to cross-functional projects within the clinical programming roadmap.
Essential Skills/Experience
- Bachelor’s degree or equivalent in computer science, life science, or statistics
- Good programming skills and prior experience in SAS/Python/R/SQL/Power BI/SpotFire and other dashboard technologies
- Basic knowledge of the clinical development process
- Good dashboard development skills in PowerBI / Spotfire
- Basic knowledge of data capture, data models, data mining
- Excellent written and verbal communication skills
- Ability to work in a global team environment
- Good analytical skills and high attention to detail
Desirable Skills/Experience
- Knowledge of industry standards
- Basic knowledge of FDA regulations and GCP/ICH guidelines related to clinical programming processes
- Prior experience and understanding of EDC systems like Medidata Rave / Inform / Veeva/ Saama/ Entimice, SAS LSAF etc.
- Knowledge of MicroStrategy
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
At AstraZeneca, we are committed to turning our life-changing science into medicines that make a difference for patients around the world. Our innovative approach allows us to manage balanced risks while spotting opportunities. We value our team's contributions in shaping drug development strategies and gaining efficient approvals. Our collaborative environment supports creative thinking and continuous learning.
-
Clinical Programmer Ii
2 days ago
Bengaluru, India Syneos Health Clinical Full time**Description** **Clinical Programmer II** Come discover what our 25,000+ employees already know: work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of. As a part of the Syneos Health team,...
-
Clinical Programmer I
2 days ago
Bengaluru, Karnataka, India AstraZeneca Full time**Job Title: Clinical Programmer I** **Career Level - C** **Introduction to role** Are you passionate about programming and clinical trials? As a Clinical Programmer I, you will support programming and validation activities for data cleaning and review listings in ongoing clinical studies. Working under the guidance of an experienced programmer, you will...
-
Clinical Data Programmer Sas
14 hours 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,...
-
Statistical Programmer Ii
5 days ago
Bengaluru, India Bayer Full time**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...
-
Clinical Data Analyst
4 days ago
Bengaluru, Karnataka, India George Clinical Full timeCompany Overview:Established in Asia-Pacific, our organization is a leading global clinical research organization driven by scientific expertise and operational excellence. With over 20 years of experience and 500+ people managing 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe, we offer a full range of clinical trial services...
-
Clinical Dm SAS Programmer
15 hours ago
Bengaluru, Karnataka, India Novasyte Full timeGood 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,...
-
Bengaluru, Karnataka, India George Clinical Full timeWe are a leading global clinical research organization, founded in the Asia-Pacific region and driven by scientific expertise and operational excellence. With over 20 years of experience and a team of 500+ people managing 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe, we offer a full range of clinical trial services to...
-
Associate Clinical Data Programmer
2 days ago
Bengaluru, Karnataka, India Novo Nordisk Full timeAssociate Clinical Data Programmer **Category**:Data & AI**Location**:Bangalore, Karnataka, IN- ..- We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.- At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for...
-
Associate Clinical Data Programmer
2 days ago
Bengaluru, Karnataka, India Novo Nordisk Full timeAssociate 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...
-
Sas Programmer/statistical Programmer
6 days ago
Bengaluru, India Quanticate Full time**Overview**: An exciting opportunity for a SAS Programmer has arisen within our Clinical Research Organisation (CRO), Quanticate. Working from our Bangalore/Hyderabad, India office, you will work within Quanticate’s global programming department, providing the highest quality statistical programming...
-
Principal clinical data science programmer
7 days ago
Bengaluru, India Trigent Software Inc Full timeTitle: Principal Clinical Data Science ProgrammerLocation: Bangalore/Chennai/Trivandrum (Remote/Hybrid)Experience: 6+ YearsAbout Us:We are a leading organization in the clinical research sector, committed to delivering high-quality data solutions. We are seeking a Principal Clinical Data Science Programmer to join our dynamic team and contribute to...
-
SDTM Programmer II
5 days ago
Bengaluru Urban, India Excelya Full timeExcelya, one of the leading independent CRO in Europe.Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop...
-
Principal Clinical Data Science Programmer
1 week ago
Bengaluru, India Trigent Software Inc Full timeTitle: Principal Clinical Data Science ProgrammerLocation: Bangalore/Chennai/Trivandrum (Remote/Hybrid)Experience: 6+ YearsAbout Us:We are a leading organization in the clinical research sector, committed to delivering high-quality data solutions. We are seeking a Principal Clinical Data Science Programmer to join our dynamic team and contribute to...
-
Principal Clinical Data Science Programmer
7 days ago
Bengaluru, India Trigent Software Inc Full timeTitle: Principal Clinical Data Science Programmer Location: Bangalore/Chennai/Trivandrum (Remote/Hybrid) Experience: 6+ Years About Us: We are a leading organization in the clinical research sector, committed to delivering high-quality data solutions. We are seeking a Principal Clinical Data Science Programmer to join our dynamic team and contribute to...
-
Principal Clinical Data Science Programmer
1 week ago
Bengaluru, India Trigent Software Inc Full timeTitle: Principal Clinical Data Science ProgrammerLocation: Bangalore/Chennai/Trivandrum (Remote/Hybrid)Experience: 6+ YearsAbout Us:We are a leading organization in the clinical research sector, committed to delivering high-quality data solutions. We are seeking a Principal Clinical Data Science Programmer to join our dynamic team and contribute to...
-
Clinical Data Programmer Iii Sas
5 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...
-
Statistical Programmer Ii
14 hours ago
Bengaluru, India Ergomed Full timeCompany Description Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you...
-
Principal Clinical Data Science Programmer
7 days ago
Bengaluru, India Trigent Software Inc Full timeTitle: Principal Clinical Data Science ProgrammerLocation:Bangalore/Chennai/Trivandrum (Remote/Hybrid)Experience:6+ YearsAbout Us:We are a leading organization in the clinical research sector, committed to delivering high-quality data solutions. We are seeking a Principal Clinical Data Science Programmer to join our dynamic team and contribute to innovative...
-
R Shiny Programmer/Senior Programmer
1 day ago
Bengaluru, India ApicalGo Consultancy Full timePrimary Purpose:We are seeking a talented R Shiny programmer to develop interactive reports that translate clinical trial data into clinical insights. As an R Shiny programmer you will design, develop, deploy, and optimize user-friendly interactive web applications for clinical data analysis and visualization. You will work closely with data scientists,...
-
Clinical Data Associate Ii
6 days ago
Bengaluru, India Novotech Asia Full timeBrief Position Description: Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements, and Novotech/Client SOPs. Minimum Qualifications & Experience: Graduate in a clinical or life sciences related...