161 Job openings found

Job Description Exp in clinical SAS, exp in SDTM(Eagle/ARDS) Level 10/9 Location – Vikhroli Responsibilities/Authorities Review and analysis of source (raw) data. Author mapping specifications from source (raw) data to target (CDISC SDTM and/or sponsor defined standards). Develop CDISC SDTM domains utilizing a data conversion tool. Quality Control of CDISC SDTM domains. Create data definition files and Case ...

?         Generate safety and efficacy tables, listings and Figures for CT Projects and stand-alone studies . ?         Validate programs and outputs of developers ?         Review Mock shells and CRF.  ?         Generate SDTM datasets and AdaM datasets as required with respect to allocation ?         Validate CDSIC datasets and programs of developers. ?         Communicate with cross functional team and sponsor if required for ...

Position:         Sr. Executive - RA Location:        Daman Experience:     8 to 12 Years Industries:      Pharma   Responsibilities: Maintaining compliance with ISO 13485, MDD, and MDR requirements. Preparing technical and device master files Preparing and compiling documents for registration to various countries Reviewing and updating of documents w.r.t various regulatory requirements Reviewing and updating ...

Description: Position:         Male Nurse Location:        Jhagadia near by Ankleshwar  Experience:    3- 5  Years Industries:     Chemical Responsibilities: Assistance in Health Check-ups Provide Assistance in carrying out all statutory pre-employment & Periodic Medical Examination (PME) at site. Regular Monitoring of Employees & workers for various hazards. Training & ...

1. NEW PRODUCT DEVELOPMENT RC grades to develop within 3 months time with commercial supply Other MCC combination product range to develop including MCC + Lactose, MCC Spheres,   Technical support including market complain to provide when & where is required Market support and explore to promote MCC, Powdered Cellulose ...

Job Description:   Position:  Sr. Officer/ Executive - RA Location:        Daman Experience:    3 to 6 Years Industries:      Pharma   Responsibilities: Maintaining compliance with ISO 13485, MDD, and MDR requirements. Preparing technical and device master files Preparing and compiling documents for registration to various countries Reviewing and updating of documents w.r.t various regulatory requirements Reviewing and updating of documents ...

Education and Experience Requirements/Qualifications:Base Level:• Bachelor’s degree or equivalent, preferably in Computer Science.• Minimum of 8 to 17 years’ experience building EDC databases in support of clinical research.• Technical EDC build experience using Medidata Rave.• Experience working on clinical trials.• Experience working in highly diverse teams within clinical research; cross-functional, ...

Minimum Requirements:• Bachelor’s degree in statistics, biostatistics, mathematics, computer science or lifesciences required.• A programming experience in industry recommended.• For US positions: US military experience will be considered towards industryexperience.• Demonstrated proficiency in using SAS, R or other programming languages toproduce derived analysis datasets and TFLs.• Understanding of clinical data ...

Skills Required - Database expert in Oracle - Professional experience and expertise in Oracle PL/SQL, scripting (SQLPlus) and writing efficient SQL queries - Professional experience and expertise in SQL query tuning and database schema design - In-depth understanding of coding languages - Determine, develop and deliver innovative strategies and tools to target new and current ...

• Deliver timely consistent, accurate and reproducible coding of clinical trial data using industry standardcoding dictionaries (MedDRA, WhoDrug) in line with global and therapeutic area guidelines.• In collaboration with Global Data Manager, develop trial coding specifications in line with trial requirementsdefining coding elements, dictionary versions and review timelines.• Complete and ...