New Jersey
Clinical Solutions Group Jobs in New Jersey
12 Clinical Solutions Group jobs in New Jersey found on Monster.
Clinical Data Manager Summary of Responsibilities The Clinical Data Manager will provide comprehensive data management expertise to Data Management to provide efficient, quality data management products that meet customer needs Essential Functions •Support Data Manager on in-house studies •Perform daily query management in RAVE for in-house studies •Provide input for negotiations with vendors •Com...
Biostatistician Large pharmaceutical company in Central NJ has an immediate for a contract Statistician.Role is initially 12 months with the option to be extended.PhD in statistics w/1-5 yrs exp in pharma industry clinical studies or MS statisticsw/3-5+ yrs. exp in pharma industry clinical studies. Clinical pharmacologystudy exp required.Contractor will support clinical pharmacology efforts. Provi...
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....
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...
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...
Sr. Statistical Programmer The Sr. Statistical Programmer will provide timely support to the study team on all programming matters according to the project strategies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. Should have the ability to generate all of the production tables needed for a given stu...
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 Central NJ has an immediate need for a contract Statistician. PhD in Statistics w/1-5+ yrs of Clinical Statistics experience within a sponsor and/or CRO environment is required. MS Statistics requires 3-5+ yrs of experience within the Clinical Statistics segment. Previous Clinical Pharmacology (PK/PD) study exp strongly preferred. Contractor will provide protocol re...
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...
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...
Large CRO is seeking an Associate Clinical Data Manager for a long term contract opportunity in Overland Park, KS. Client requirements: 5+ years experience in Data Mgmt including managing project timelines, quality issues, resource mgmt, CRF design, discrepancy mgmt, locked databases, study start up through database locks. The candidate will mentor other team members and Lead Data Managers in trai...
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...
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©2013 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2013.1.5.22-327