At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
Total Years of Experience - 4+ Relevant Years of Experience - 4+ Location - BLR - WFO No. of positions -3 Contract length - 6 Months Interview Mode-Virtual Notice-Immediate to 10 Days MAX. Shift-General. CTC-9 LPA(Max
Job Title - Digital R&D Integration Manager Location - Hyderabad Department / Organization Organization: Digital R&D — Software Engineering Sub-Domain: Data Integration Engineering Business Context: Sanofis Digital R&D organization is at the forefront of transforming drug
Responsibilities: Analyze data and report statistical results. Develop SDTM specifications for programming datasets following CDISC standard. Independently develop SAS programs to create SDTM datasets. Develop ADaM analysis data specifications for programming following CDISC standard with minimum supervision. Independently develop SAS
About Regeneron Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change
External Job Description As a Principal Statistical Programmer within our Hyderabad Hub, you’ll 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
OVERVIEW The Data Engineer, Sr - I will work closely with clients and provide high level technical consulting services, configuration of the elluminate® platform, development and oversight for specific projects that include trial configuration, quality control,
eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud – the foundation of digital trials. Together, the elluminate platform and digital data
About the Job Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand
About the Job Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand
About Value Spire Value Spire is an early-stage technology company focused on supporting clients specialized in clinical trial intelligence. We are actively recruiting for one of our prestigious clients building a platform that reduces the time,
Job Description Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve peoples lives. A biotechnology pioneer since 1980, Amgen has grown
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Involves in the development, validation, and review of study & standard programs/macros (Including SAS, CQL, PL/SQL, SPOTFIRE, R-Programming, Python) that support standard and study-level conversion of clinical trial data. Responsible for the review, development, and validation of SDTM mapping,
Key Responsibilities:: Involves in the development, validation, and review of study & standard programs/macros (Including SAS, CQL, PL/SQL, SPOTFIRE, R-Programming, Python) that support standard and study-level conversion of clinical trial data. Responsible for the review, development, and validation
We are looking for an experienced Clinical Data Engineer to join our clients growing Clinical Data Sciences team. The ideal candidate will have strong expertise in building scalable clinical data pipelines, cloud-based data engineering solutions, and
Medtek Dot AI Pvt limited is a data science consulting company supporting global Pharma and Biotech companies. Our mission is to help “Unlock insights and drive innovations” using the data collected. We are a team of
Title: Senior/ Principal Statistical Programmer(R) Location: Remote Duration: Long Term Contract Salary: Open Experience : 6-10+ Years Notice : Immediate OR Within 15days Requirements We are looking for Senior / Principal Statistical Programmer(s) with strong hands-on