271 Cdisc Jobs - Page 2

Design, develop, and implement clinical SAS programs for data management and analysis. Develop and maintain complex SQL databases for data storage and retrieval. Required Candidate profile Strong expertise in CDMS, clinical SAS programming, and SQL database management. Experience working with large datasets and developing complex data models.

Analyze and interpret complex clinical trial data using SAS. Develop and maintain databases, data systems, and computer models for clinical trial management. Collaborate with cross-functional teams. Required Candidate profile Strong proficiency in SAS programming language. Experience with Veeva or similar clinical trial management systems. Excellent analytical, problem-solving, and communication skills.

Design, develop, and implement clinical trial data management systems using SAS. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the development process. Required Candidate profile Strong proficiency in SAS programming language and its applications in clinical trial data management. Experience with SQL programming language and its applications in statistical analysis.

Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to ensure seamless integration of Veeva EDC ystems. Required Candidate profile Strong understanding of Veeva EDC principles and technologies. Experience with clinical trial data management systems. Excellent problem-solving skills and attention to detail.

Design, develop, and maintain SAS programs for clinical trial data management and analysis. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and implement data validation and quality control Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management and analysis. Experience working with clinical trial databases and data management systems.

Design, develop, and implement clinical trial data management systems using CDMS expertise. Collaborate with cross-functional teams to ensure seamless integration of clinical trial data into the overall study design. Required Candidate profile Strong understanding of clinical trial data management principles and CDMS expertise. Proficiency in SAS programming language with experience in developing complex statistical analysis plans.

Design, develop, and implement clinical SAS programs for data management and analysis. Develop and maintain complex SQL databases for data storage and retrieval. Collaborate with cross-functional teams to identify business requirements Required Candidate profile Strong proficiency in SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience with SQL database management systems, including design, development, and maintenance.

Design, develop, and maintain SAS programs for clinical trial data management and analysis. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and implement data validation Required Candidate profile Strong knowledge of SAS programming language and its application in clinical trial data management and analysis. Experience working with clinical trial databases and data management systems.

Role Overview: As a Senior Scientific Manager, Clinical at Elucidata, you will be responsible for acting as a Technical Owner for clinical data programs. You will lead a small team, set the technical direction, and ensure delivery quality and timelines. Your role will involve collaborating with various teams to design and implement scalable clinical and real-world data solutions. Key Responsibilities: - Design and implement scalable clinical and real-world data solutions across EHR, claims, registries, and trial datasets. - Develop and maintain data models (conceptual, logical, and physical) to ensure accuracy, consistency, and integrity across systems. - Standardize and integrate clinical d...

Main responsibilities: The Senior Statistical Programmer will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans and provide QCd data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, manuscripts and ad-hoc data analysis requests); The Senior Statistical Programmer will develop, implement, and document non-routine macros and advanced techniques; The Senior Statistical Programmer will ensure SOPs are followed and timelines and quality are met. People: 1) Develop and maintain effective relationships and c...

Hiring for No-1 IT MNC for Clinical SAS Programming Salary Up-to - 30LPA + NSA Any Grad/ PG With 5 Yrs Of experience In SDTM , ADAM , TLF , SAS MACROS CDISC standards etc Call @ WhatsApp- Shubhani - 8595849767 Call @ WhatsApp- Sejal -8595347527 Perks and benefits General Shifts Both Side Cabs Insurance etc

As a Statistical Programming Intern, your role involves providing robust statistical programming support for multiple clinical projects using SAS to deliver key regulatory-compliant outputs. You will be responsible for developing programming documentation, writing efficient code, and staying updated on statistical programming techniques. Your duties also include providing study updates to the study lead while performing your assigned tasks. - Provide statistical programming support for multiple clinical research study projects or study teams under the oversight of the lead programmer. - Support key deliverables based on regulatory requirements for clinical research e-submissions and/or study...

Job Description Who Are You An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead one Phase I-IV clinical studies across your region. You are excited and enthusiastic, motivate your teams to do great work and collaborate easily with your clients. You never settle for what is, but always push clinical development forward to what it could be. You motivate others to do the same. Sponsor-dedicated Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Biostatistician you will be dedica...

Who We Are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. Th...

Role Overview: You will be working as a Senior Manager, Statistical Programming, providing comprehensive programming leadership for programming deliverables within a product/program. Your role will involve managing the timely and accurate execution of programming components of clinical trials to support the development, regulatory approval, and market acceptance of Teva Products. You will also lead and manage projects that involve global tasks, cross-functional teams, or outsourcing resources. Key Responsibilities: - Primarily work at the product/program level - Manage and deliver assignments with quality and within timelines, providing input for budget planning - Independently develop, vali...

Who We Are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. Th...

Role Overview: ZS is a management consulting and technology firm that focuses on transforming ideas into impact by utilizing data, science, technology, and human ingenuity to deliver better outcomes for clients worldwide. As a part of ZS, you will work alongside a collective of thinkers and experts to create life-changing solutions for patients, caregivers, and consumers. Your role will involve designing and implementing innovative solutions in clinical trials, data management, and analytics. Additionally, you will lead technology projects, collaborate with clients, and contribute to the growth of a Business Analysis community. Key Responsibilities: - Design and implement innovative solution...

The Statistical Programming Intern provides robust statistical programming support for multiple clinical projects using SAS to deliver key regulatory-compliant outputs. Key responsibilities include developing programming documentation, writing efficient code, and staying updated on statistical programming techniques. This role also provides study updates to study lead while performing assigned duties. Provides statistical programming support for multiple clinical research study projects or study teams under oversight of lead programmer. Supports key deliverables based on regulatory requirements for clinical research e-submissions and/or study requirements for Sponsor, Regulatory, Investigato...

Statistical Programmer will be responsible for developing, and validating SAS programs in support of clinical research. The role includes programming of SDTM and ADaM datasets, TFLs, and PK-PD analyses. Send your resumes to hr@novanal.com

The Data Modeler will work on projects to define and develop logical and physical data models that satisfy Parexel's financial and operational reporting, analytic and integration needs. The Data Modeler will contribute to the overall data models and define principles, designs, and models that drive information sharing across the enterprise. Essential Job Responsibilities Working with business subject matter experts and IT groups to document data attributes and requirements. Understanding and translating business needs into data models which support long term solutions. Creating logical and physical data models to support new and existing projects. Documenting logical and physical mapping def...

Our Team About the job Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main Responsibilities The Principal Statistical Programmer will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans and provide QC'd data packages in...

Data Architect Key Responsibilities Design architectures for modern ecosystems (Data Lakes, Mesh, Fabric) which drives the long-term strategy for LRL Data. Embed pharma-specific standards (CDISC, FHIR, HL7, Allotrope, etc.) into designs. Drive governance, lineage, and compliance via MDM and quality frameworks. Influence leadership and stakeholders on data strategy and best practices. Lead large-scale data transformation, ETL, and pipeline design. Architect and maintain enterprise data models (relational, dimensional, big data). Partner with solution architects, business SMEs, and engineering teams to design conceptual, logical, and physical models that align with pharma standards and governa...

This job is with Pfizer, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Summary An Individual Contributor role Productive hands on programming, supporting deliverables in the study/project/portfolio/standards team, of medium - high complex statistical programming deliverables to support assets and study teams Performs tasks with limited supervision early in role and independently later in role. Is capable of handling standards/study programming specific activities independently including collaboration across stakeholders at various timezones Ensures adherence to high quality programmin...

As a Principal Statistical Programmer within our Hyderabad Hub, youll be part of a performing team, delivering biostatistics and programming activities throughout the Vaccines R&D value chain (Pre-Clinical, Clinical, Translational, CMC) with our Vaccines Global Biostatistical Sciences team. We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients arou...

Main responsibilities: The Principal Statistical Programmer will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans and provide QCd data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, manuscripts and ad-hoc data analysis requests);The Principal Statistical Programmer will develop, implement, and document non-routine macros and advanced techniques; The Principal Statistical Programmer will ensure SOPs are followed and timelines and quality are met; Collaboration of Local biostatistics and programming ...