Recruiting for per-diem and full-time Anesthesiologists for a rapidly growing Anesthesia services firm. Clients in both Hospital and Ambulatory settings. Responsibilities: Determines and prescribes kinds of anesthetics and procedures to be employed in various categories of cases. Advises Anesthetists and Surgeons in cases where age or condition of patient presents unusual or complex problems. …
Read more »Long-term Contract Based in NJ Hourly Rate$55-$65/hr To support Oncology Data Operation team by managing and implementing new methodology to create and maintain tools with proper security. Responsible for providing support for clinical studies within designated EDC systems according to Oncology’s processes and standards. The responsibilities includes Clinical study maintenance, user support, testing, collaboration with …
Read more »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 dictionaries …
Read more »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, …
Read more »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 …
Read more »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 …
Read more »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. …
Read more »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 …
Read more »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, …
Read more »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 …
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