Clinical Programmer - Berkeley Heights

This is a job for Clinical Programmer. Experience in Medical Affair and Oncology Studies are preferred. · Develop, program, test and maintain clinical trial databases and data entry screens using Oracle Clinical or Central Designer in accordance with Celgene standards · Review co ...

Clinical Programmer needed for one year with possible extension. · Candidate should have a BS/BA degree or equivalent in a relevant scientific discipline with a minimum of five years experience. · ...

Clinical Programmer job in Berkeley Heights. Work from home but required to be onsite when company lifts work-from-home restriction. · ...

We are one of the fastest growing IT Consulting company across the USA and we are hiring Business Support Associate for our client.We offer a wide gamut of consulting solutions customized to our 450+ clients ranging from Fortune 500/1000 to Start-ups across various verticals like ...

We are looking for a EDC Clinical Programmer not a SAS Programmer. · Must have experience programming an EDC clinical database & setting up EDC studies. · Looking for Oracle Central Designer and Oracle Inform experience. We would consider a candidate with Medidata Rave experience ...

We are looking for a EDC Clinical Programmer, not a SAS Programmer. Must have experience programming an EDC clinical database & setting up EDC studies. · Looking for Oracle Central Designer and Oracle Inform experience. We would consider a candidate with Medidata Rave experience, ...

Clinical SAS Programmer responsible for designing and coding SAS programs for clinical projects. · ...

The Clinical Database Programmer will lead the development and maintenance of database builds in support of clinical studies. He/She will build study databases including development of database specifications/definitions, programming of CRF layouts, programming of validation and ...

Job summary · Clinical SAS Programmer Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). · Produces and delivers CDISC and regulatory compliant SDTM, · and ADaM standard datasets. · Cr ...

We are hiring Clinical Statistical Programmer for one of our clients. · B.S. or equivalent in computer science, mathematics, or life science. · A minimum of 5 years of relevant clinical research programming experience. · ...

The Clinical Database Programmer will lead the development and maintenance of database builds in support of clinical studies.He / she will build study databases including development of database specifications/definitions, programming of CRF layouts, programming of validation and ...

We believe in providing staffing solutions to address the current talent gap right talent right time right place right price and acting as a career coach to our consultants. · Interface/liaise with a variety of end users and can think holistically about data review approaches tha ...

Accountable for setting up studies & developing standard programs to create reports listings graphs metrics for clinical data management and other areas of clinical for data review and data cleaning to conduct clinical trials in Oncology area within JReview environment. · We do o ...

This Senior Data Manager role involves managing outside CROs and consultants, performing QC of CRO activities, monitoring progress of data management activities, interacting with CRAs, programmers, study managers and statisticians in creating an appropriate database. · ...

Sr Data Manager will manage outside CROs and consultants by performing QC of CRO activities, monitoring their progress and participating in regular team meetings. · ...

+We are one of the fastest growing IT Consulting company across the USA and we are recruiting RAVE Programmer/Study Builder for one of our clients. · +Rave global library and edit check programming (including best practices, efficiencies and reusability) · , Develop program test ...

Create SDTM validation tools and write SAS programs to generate derived analysis datasets. · Demonstrated proficiency in development and validation of SAS macros. · In-depth understanding of SDTM, ADaM, and submission requirements. · ...

This role will support the overall Clinical Study Subject Narratives Process within Hematology/Oncology by authoring and coordinating Clinical Study Subject Narratives for assigned studies. · ...

We are hiring for EDC Programmer (Clinical) at Irvine, CA or Madison, NJ. · Responsibilities:Leading internal and outsourced Clinical Programming activities in support of Clinical Research studies. · ...

Lead statistical programmer with 10 years of experience in clinical/pharma domain required for Net2Source Inc. · ...