Work ScheduleSecond Shift (Afternoons) Environmental ConditionsOffice Job DescriptionJoin Us as a Clinical Data Managemnet Programmer I Make an Impact at the Forefront of Innovation The Clinical Data Managemnet Programmer I works with clinical data management systems and programming
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
Project Role: Rave Programmer Work Experience: 1 years Work location: Any IQVIA office Location in India Work Mode: Hybrid Must Have Skills: Rave, Edit checks RESPONSIBILITIES : • Plan and coordinate database design, development, implementation, maintenance, and
Job Description : Work Schedule Standard (Mon-Fri) Environmental Conditions Office 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
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
Support DM-related activities and collaborate with Lead DMs, Clinical Programmers, Data Scientists, Clinical Monitoring teams, and other functions like Project Management, Clinical Operations, and Biostatistics • Provide regular updates to Lead DM on progress, timelines, risks, and
Project Role: Sr Programmer - Rave Work Experience: 4 - 10 years Work location: Any IQVIA office Location in India Work Mode: Hybrid Must Have Skills: Rave, Edit checks, Customer function , Migration Job Description Read, Understand
Project Role: Programmer Work Experience: 2 to 8 Years Work location: Any IQVIA office Location in India Work Mode: Remote/Hybrid Must Have Skills: Data Acquisition, , data transfer, handling blinded data, quality assessments. Job Overview: • Plan
IQVIA is a leading global provider of advanced analytics, technology solutions and contract research services to the life sciences industry. Formed through the Merger of IMS Health and Quintiles, IQVIA applies human data science – leveraging
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
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,
Job Overview To act as a SPOC/technical SME for all prevailing EDC platforms with respect to validation scope of activities. Play major role in facing Customer Audits, Internal QA Audits etc. Essential Functions • Attend Kick
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