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Data Entry Specialist 6-12 month Contract – NJ Duties: Entering data from existing spreadsheets or correspondences to another spreadsheet. Able to work with multiple spreadsheets at a time. Entering names, selecting from drop down menu in Excel, dates, etc. May import data to another file as well. Superior accuracy and attention to detail skills. • …

Biostatistical Programmer 1 Year Contract – NJ To support the Biostatistics team by carrying out and overseeing programming activities of statistical programmers and external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies. Contributes to the overall efficiency and best practice running of the Biostatistics group, demonstrating the …

SAS Programmer Analyst 1 Year Contract – NJ   Duties: Programming reviewer and QC/ Junior SAS programmer — Primarily works with Statistical programmers on ongoing clinical studies. May work with medical writing, clinical operations, and other clinical staff to support deliverables. Must work well both independently and with team members. Needs to be able to …

Associate Director/Director Biostatistican 1 Year Contract – NJ Description Candidate in this position will be providing support to the IMI-EPAD (Innovative Medicines Initiative – European Prevention of Alzheimer’s Dementia) consortium. This senior level contract statistician will: – Support group by  reviewing key documents, as well as be part of the Work group on statistical engine …

Sr. Publishing Specialist 1 yr Contract – NJ   Duties: The Senior Publishing Specialist will be part of the Regulatory Operations Publishing Group and to ensure that dossier is prepared ready to submit to the FDA and other agencies. This includes: Publishing(Bookmarking and Hyperlinking) and Peer Reviewing different types of document like (eg Clinical Study …

Biostatistical Programmer 1 yr Contract – NJ   Duties: To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications. Contributes to the overall efficiency and best practice of the Biostatistics group, …

Clinical Study Manager 1 Year Contract – NJ   Duties: Accountable for the overall management of all assigned clinical studies, in accordance to SOPs. Study Manager must have the ability to work semi-autonomously with strong organizational, prioritization and analytical skills. Must be comfortable collaborating with other functional teams to coordinate the development and finalization of …

Communications/Public Relations Consultant 6mos – 1 yr Contract – NJ   Duties: Assist sales and marketing management with communications media and advertising materials to effectively represent the company’s products and services to customers and prospects. More specifically: 1. Experience in promotional material development including: Working with/in ad agency Reviewing materials with CRC- Copy Review Committee …

Documentation Coordinator 1 Year Contract – NJ Duties: Global Regulatory Department Perform daily document management activities such as Review, Processing, Filing of Clinical Trial Master File documents. Quality Control review of Regulatory Documents. Coordinate with eTMF vendor for TMF set-up and processing of TMF documents. Development of user manuals. Scanning and storage of Clinical Operation …

Financial Analyst 1 Year Contract – NJ Duties: • Preparation, communication and consolidation of the Annual Business Plan o Preparation of monthly, quarterly, full year and 18-month forecast in accordance with the submission timeline. o Build and maintain forecasting models for headcount, payroll, and expense accounts. o Variance explanations of actual performance against prior period, …