Contract Role Based in Northern, NJ — Remote ok Must have at least 10 years of assigning standard terminologies within Clinical Research, familiar with protocol and CRF designs. Adequate knowledge of ICH guidelines. Ensures verbatim /reported terms are adequately reported and able to assign MedDRA or WHODD terms. Responsible for resolution of PT in …
Read more »Payroll Systems Analyst/Consultant 6 + months – NJ Hourly Rate: $90-$105hr.+ ESSENTIAL DUTIES AND RESPONSIBILITIES: * Evaluate, troubleshoot, correction and configuration of system challenges * Assist with the evaluation / documentation of operating procedures department. * Analyze and document the pay conditions configured Ultimate Software, continuously identify the needs of operations, …
Read more »Consulting role based in NJ $90-$105/hr+ Summary: Work with the clinical study team on study design, development and/or review of clinical study protocols. Contribute to clinical trial design, protocol concept sheet and protocol development Participate study related activities and provide statistical support such as reviewing Case Report Form (CRF) and guidance, validating randomization scheme and …
Read more »Long-term Contract with Pharmaceutical firm in NJ $80/hr+ Work with IT and clinical teams in the development and support of Global Clinical Data Management, Clinical Pharmacology, and Biostats Systems. Plan and coordinate system design criteria, development, implementation, maintenance, and support of new or upgrades of existing systems. Provide technical expertise to the project teams …
Read more »Contractor role with global Pharma 1-3 year project $80-$85/hr DOE To support the Oncology Business Group Biostatistics team by carrying out and conducting programming activities of statistical programmers, and coordinating with external vendors (as required), Statisticians, and other business functions to ensure timely and accurate programming and validation activities for clinical studies. Contributes to …
Read more »Senior Analyst, SAP FICO – Exton, PA 1 Year Contract Role is with a Pharmaceutical Client at their R&D manufacturing facilities located in Exton PA and is kicking off a project in early May 2017 time frame to set up SAP capabilities in order to be able to manufacture commercial product. SAP is already utilized at this …
Read more »Sr. SAS Programmer Analyst (JReview/listings) – NJ 1-3 Year C2C accepted Perform SAS programming to provide data review complex listings/reports to support Data Management, Medical Coding, and other areas of Clinical functions for Oncology trials. Develop programs & graphs in JReview for easier data review and visualization. Develop programs for patient profiles and ad …
Read more »Senior Biostatistical Programmer – Oncology 1-3 year Contract – NJ Summary: To support the Oncology Business Group Biostatistics team by carrying out and conducting programming activities of statistical programmers, and coordinating with external vendors (as required), Statisticians, and other business functions to ensure timely and accurate programming and validation activities for clinical studies. Contributes to …
Read more »Senior IT Quality Validation Consultant – NJ 1+Yr Competitive Hourly Rate Duties: Perform validation activities related to Oncology trials for EDC studies. • Prepare specification documents, Plans, Test scripts, Summary reports • Conduct tester training and coordinate testing effort • Manage study specific validation documents within Data Management area • Ensure all the validation deliverables …
Read more »Description: Looking for a strong solution architect to lead IT initiatives for many of the Commercial business functions including Sales, Marketing, Medical, and Market Access. The resource will be responsible for the specific initiatives below when they join. 1. Leading a KOL mapping initiative which includes deploying Veeva Medical as well as an integrated KOL …
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