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
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Project Role: Programmer Work Experience: 5 to 10 Years Work location: Bengaluru. Work Mode: Remote Must Have Skills: Data Acquistion, , data transfer, handling blinded data, quality assessments. Job Overview: • Plan and coordinate database design, development,
Project Role: Rave Custom Function Programmer Work Experience: 5 to 8 Years Work location: Bengaluru. Work Mode: Hybrid Must Have Skills: Rave, Custom Function Job Overview: Read, Understand and program Medidata Rave Edit checks and custom function
Work ScheduleSecond Shift (Afternoons) Environmental ConditionsOffice Job DescriptionJoin Us as a CDM Programmer II Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a CDM Programmer II – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a CDM Programmer II – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning
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
Job Overview Conduct testing activities and provide comprehensive testing expertise to produce efficient, quality database that meets customer requirements. Provide support in creation of Test Plan and handling of validation projects. May act as Validation Team
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
About the role: The Team Lead Data Management will have responsibility for Data Management staff as assigned and ensures that line reports conduct clinical trials according to all applicable Good Clinical Practice (GCP), Regulatory Requirements, Standard
Work Flexibility: Hybrid What You will do: This position leads in-house statistical and analytical services in RWE studies, participates in RWE projects within Clinical Affairs and takes part in cross-divisional collaborations with RWE relevance. Working with
Project Role: Rave Custom Function Programmer Work Experience: 5 to 8 Years Work location: Bengaluru. Work Mode: Hybrid Must Have Skills: Rave, Custom Function Job Overview: Read, Understand and program Medidata Rave Edit checks and custom function
When our values align, theres no limit to what we can achieve. The Senior Clinical Database Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas
When our values align, theres no limit to what we can achieve. The Principal Clinical Database Programmer will be recognized as a subject matter expert, providing technical support and expert advice to internal and external sponsors. In
When our values align, theres no limit to what we can achieve. The Clinical Database Programmer II provides technical expertise for the conduct of clinical trials and works with minimal supervision to support various programming activities related
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. We are looking for Clinical Data Manager
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