Archives

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 …

Terrific opportunity in the Finance Department of a Global Pharmaceutical firm!   Performs daily activities for 5 bi-weekly and semi-monthly payrolls to ensure accurate and timely compensation to employees for work performed. Performs a variety of statistical tasks and clerical duties required to prepare payroll data for computer input. Reviews timekeeping records. Processes exception items …

Clinical Research Associate – NJ 1-3 year Contract $65-$70/hr Duties: Assist in the management of the day to day operations of clinical trials including coordination and oversight of all CRO/clinical site/vendor activities, liaison between Clinical Operations Manager and CRO, manage scopes of work/budgets/invoice payments. Assist in the management of the Trial Master File (submit documents, …

Director, Sr Director, VP Medical Affairs/Strategy   Our client  is multinational specialty pharmaceutical company with  a diverse product portfolio with focus on branded pharmaceuticals, branded generics and over-the-counter products. Specialization in dermatology, eye health, neurology  gastroenterology, hepatology and consumer healthcare.  Reporting to the Sr. Vice President Medical Affairs, this position will build and maintain solid …

Global Labeling Manager – NJ Contractor (1-3 years) Hourly Rate: $60-$65/hr   Duties: Facilitate and lead the development, review, approval, and maintenance of the Company Core Data Sheets (CCDS) and Country Product Information (CPI) and CPI components for assigned products either globally as a Global Labeling Lead or regional/local as a Regional Labeling Lead. Functioning …

Project Coordinator, Corporate Ethics and Compliance – NJ 1Year Contract – $30-$35hr DESCRIPTION: The Project Coordinator, Corporate Ethics and Compliance, will report to the Executive Director, Corporate Ethics and Compliance (CECD), and assist with the development and implementation of programs supporting the Corporate Ethics and Compliance Program. General responsibilities include: Initiation and review of healthcare sanction …

Product Safety Data Coordinator and Coding Associate – Remote (onsite in NJ 1 day per week) 1-3 year Contract Competitive Hourly Rates   Duties: Data entry into the Product Safety database for Adverse Events reported in association with marketed and investigational products. The activities include, but are not limited to, data entry, coding into standard …

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 …

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 …

Manager, Biostatistician – NJ 1+year Contract $90- $100hr++ Duties: 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 …