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Long-term Contract Role Hourly Rate $70/hr Based in New Jersey Responsibilities: Under the supervision and guidance of a manager, apply clinical/medical background to review medical conditions; assist and perform coding using a standard medical dictionary (MedDRA, WHODD); perform reconciliation between clinical database and CIOMS; review patient records to identify discrepancies, inconsistencies, or missing data; review …

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 …

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. …

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. …

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 …

Contract role – 1year – $30/hr++ Woodcliff Lake, NJ This position provides administrative support to expatriate(s) and executive visitors from home office in Japan. This person will also provide other supports where Japanese language skills are required including but not limited to translation of business documents, communication support by summarizing Japanese to English (vice versa) …

This is a 6 + month Contract role based in NJ Hourly Rate $70/hr Summary: The Project Manager is accountable for supporting Sales, Marketing and Operations to set up National Sales Meetings. Responsibilities: – Attend weekly planning meeting with cross functional teams within, Sales, Marketing and Operations to plan National Sales Meetings. – Ensure cross …