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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 …

Clinical Research Scientist – Contractor $70/hr+ NJ   Duties: The incumbent is responsible for, but not limited to the following: • Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies • Prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of …

Clinical Research Associate – 1+ year Contract Hourly Rate: $60/ hr++ NJ • 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 …

Our client, a family owned Dental Office is looking for a part-time  receptionist for their rapidly growing office in Wappinger Falls, NY. Job description: This employee will perform routine front desk tasks including: Providing excellent customer service and being the face and voice of the practice Greeting patients and helping new patients with registration Checking patients out …

Medical Information Specialist – Contractor Based in Northern, NJ Job Summary The Medical Information Specialist is responsible for meeting the medical information needs of external customers and internal business partners as it relates to the company’s products. He/she will contribute to the development of high-quality Medical Information deliverables within the team and will be a …

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 …

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 …

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 …