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Sr. Manager, Data Management – Contractor 1+year – Based in Woodcliff Lake, NJ – $70-$80hr   The Neuroscience and General Medicine product creation group  is currently looking to fill a Sr. Manager, Data Management opening at its North American Headquarters in Woodcliff Lake, NJ. Duties: Contribute to protocol, and create study and therapeutic specific documents. …

Global Labeling Manager  – Consultant – NJ $70-$75/hr Description:   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 independently as …

Junior Accountant – 3 Month Contract Andover, MASS   Junior Accountant needed for assistance with vendor communications such as requests for missing invoices or aging reports. Strong attention to detail and good communication skills. Some Excel sheet data entry will be required to help with monthly journal preparation. Assistance with administrative duties for month end …

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, …

Sr. Clinical Study Manager – Neuroscience – Contractor (NJ) $70hr-$80hr Description: This position is responsible for supporting 2 pivotal phase 3 registration clinical trials as the North America lead, one of which is in set up and one in MAA submission preparation activities including but not limited to, as outlined below: Experience in managing all …

Sr. Clinical Data Manager, Oncology – Contractor – NJ $65-$70/hr Job Description: Responsible for clinical data management activities for studies and ensuring FDA requirements for quality databases submissions are met. Perform and manage clinical Data Management (DM) activities for in-house and outsourced trials including protocol review, CRF (Case Report Form) development, database set up activities, …

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 …

Growth Opportunity with Large Pharma in NJ Full-time role Responsible for implementing publication planning activities and deliverables to meet the needs of external customers and internal business partners for assigned products. The manager will be responsible for coordination and management of cross-functional publication teams and ensure that there is no overlap/redundancy in global publication activities. …

Temp to Perm role with Large Pharmaceutical firm in NJ This position requires an in depth “hands’-on” operational knowledge of Customer Service. Position has multi-faceted responsibilities ranging from strategic to operational. The role is the first-line customer contact and required to investigate and resolve a range of issues across both external customers and internal stakeholders …

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 visible member of the department by collaborating cross-functionally to meet Medical …