At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. The Senior Clinical Programmer I (SrCP1) develops and coordinates clinical programming
Senior Clinical Programmer (Power BI, Python Prog) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them
Job Description SummaryResponsible for configuring and managing the Central Monitoring Platform by translating study requirements into data-driven solutions, while developing and maintaining Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and Data Quality Analytics/Statistical Monitoring tests
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
About the Role: The CDP-II is responsible for the design, development, programming, validation, and maintenance of clinical trial databases throughout the study lifecycle. This includes clinical database build, Case Report Form (CRF) design, edit check programming, custom function
About the Role: The Clinical Programmer (SDTM) is primarily responsible for SDTM programming based on Clinical Protocols, eCRF and Statistical Analysis Plans. The Clinical Programmer (SDTM) may also be responsible for data submission packages to clients and regulators. The Clinical Programmer (SDTM) works
Join a dynamic and growing clinical research organisation at the forefront of data-driven innovation in clinical trials. We are committed to delivering high-quality, reliable data solutions that accelerate drug development and improve patient outcomes worldwide. Our collaborative, fast-paced
Clinical Database Programmers are operationally responsible to provide technical support and oversight for the Medidata Clinical Cloud (MCC) implementation activities. Clinical Database Programmers will maintain project level perspective, focus and communicate effectively as the MCC SME on technical and functional electronic
Senior Lead Clinical Data Science Programmer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Senior Lead Clinical Data Science Programmer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Project Role: Software Devl Analyst 2 (Python & R Programmer) Work Experience: 5 to 8 Years Work location: Bengaluru. Work Mode: Hybrid Must Have Skills: Python is mandatory skill along with Clinical Data Management or Clinical Domain Job Description
Work ScheduleSecond Shift (Afternoons) Environmental ConditionsOffice Job DescriptionJoin Us as a Senior Clinical Data Managemnet Programmer I - Make an Impact at the Forefront of Innovation The Senior Clinical Data Managemnet Programmer I works with clinical data management systems and programming
Statistical Programmer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart
Statistical Programmer – L2 Job Summary: Statistical Programmer reports to Principal Statistical programmer 3/ Lead, Statistical Programming (L4 (3) or M1), is responsible to work independently on the most of the Mapping activities (SDTM/Client specific mappings) which are simple
Job Overview Responsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In
We are seeking highly experienced SDTM Programmer candidates with minimum 6 years of relevant experience CRF annotation Strong understanding of CDISC standards, including the SDTM Implementation Guide and regulatory authority submission guidelines Hands‑on experience in developing, validating,
Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, youll be at the heart of our clients innovation. As a Principal Statistical Programmer you will be dedicated to
Statistical Programmer II Introduction to role: Are you ready to turn clinical data into reliable evidence that speeds medicines to patients? Do you thrive in a high-learning environment where your code directly shapes trial decisions and future submissions?
Statistical Programmer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart
Work Flexibility: Hybrid Job Summary This position is responsible for providing statistical guidance in development of clinical research programs and of individual studies as part of multi-disciplinary team. This role involves the development of Statistical Analysis Plans,