Clinical Solutions Group Jobs in Bridgewater

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7 Clinical Solutions Group jobs in Bridgewater, New Jersey found on Monster.

Jobs 1 to 7 of 7
Growing pharmaceutical company with multiple stateside sites has an immediate need for a perm based PhD level Sr. Biostatistician in their North/Central NJ facility. Previous oncology experience is required. Top pay and relocation assistance available. The Sr. Biostatistician implements and executes methodological and statistical aspects of clinical studies with direction from Therapeutic Area lea...
CMC Regulatory Specialist Large pharmaceutical company in Central NJ has 4 immediate needs for contract based CMC Regulatory Specialists. 1 opening requires hands on Biologics experience. Roles are approved through year end with the option to be extended. Duties: The candidate will be responsible for preparing global CMC regulatory submissions for COMPANY’ marketed drug products. The position will...
Large pharmaceutical company in Hopewell, NJ has an immediate need for a contract SAS Programmer. 100% onsite. Role is initially 12 months with the option to be extended. Seeking candidates who possess 9+ years of stateside TLG Programming experience within sponsor and/or CRO environments. Must possess experience creating SAS datasets, generating TLGs/reports, validating other programmers' output,...
Large pharmaceutical company in greater Princeton area has an immediate need for a contract SAS Programmer. Seeking candidates who possess 9+ years of stateside TLG Programming experience within sponsor and/or CRO environments. MS grads preferred, but not required. Must possess experience creating SAS datasets, generating TLGs/reports, validating other programmers' output, adhering to CDISC standa...
Sr. Study Manager The Study Manager is responsible for • Leading one or several cross functional study teams (and/or sub-teams) to deliver clinical research studies on time, within budget and with good quality in compliance with Regulatory Authorities regulations/guidelines and Celgene SOPs/WPs. • Sharing best practices • Contributing to process improvement initiatives Study Manager Responsibiliti...
Large pharmaceutical company in Central NJ has an immediate need for a contract based SAS Programmer. Role is approved through year end with the option to be extended. Prefer MS level grads, but will consider BS level candidates. Prospects must possess 5+ years of SAS programming experience within an Outcomes Research or Analytics department within a sponsor or specialty firm. Candidates must have...
Manager of Medical Information Through decades of combined experience, CSG, Inc. understands the intricacies of the drug development process, industry-based technologies, and the responsibilities tied to the positions we support. This has helped our firm gain credibility and notoriety with key decision makers within Pharmaceutical companies ranging from small start-ups to fortune 500 corporations....

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