Temporary, Contract, Project Assistant Manager jobs in the Biotech, R&D, Science category in Hackensack, New Jersey

DESCRIPTION We are looking for talented and creative professionals in the flavor and fragrance industry for R&D and Quality positions in the lab. The ideal candidate needs to have a positive energy and be ready to work as part of a fast paced team. We are currently considering local candidates only! This job entails: • Preparing product in accordance with batch record formula • Supporting special ...
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Great opportunity for an experienced Clinical Data Manager! Excellent work environment! Long-term contract opportunity! Title: Senior Clinical Data Manager, Oncology Project description: -Project Data Management level. Assist Associate Director oversee other data managers on a project. -Perform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up acti...
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Job Description: The CEP (Customer Engagement Programs) Review and Remediation Project Manager will support the global project for assessment, review, and remediation of CEPS by tracking and coordinating activities related to this project. This role reports to the CEP BPO Key Responsibilities • Create a process to track and prioritize review and remediation activities that arise from the Global MQ...
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Global Pharmaceutical company is seeking a clinical project manager (PM) for a long term contract to provide Project Management and Continuous Improvement (CI) expertise (e.g. DFSS, Lean, Six Sigma) and aid in embedding a CI culture within Development Operations. The PM/CI Specialist leads the global development (and implementation as appropriate) of large-impact continuous improvement business pr...
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COMPANY PROFILE Sound Advice is a boutique consulting services firm headquartered in New York with a national presence. We have a reputation for quality and excellence in the Pharmaceutical and Life Sciences space. Sound Advice has a long term strategic partnership with one of the world’s largest and most respected Pharmaceutical companies, headquartered in New York City. We have been engaged to p...
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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...
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Requirements: Bachelor's degree 5-10 years of experience in clinical data management role Thorough knowledge of ALL of data management processes from study start up to study close out Previous experience in managing delivery of projects through full data management study life cycle (Phase I and II or Phase III) Experience working on both paper and electronic data management studies Direct experien...
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Requirements: Bachelor’s degree 5 years experience as a data coordinator Strong documentation and project management skills Responsibilities: Act as point person for plan sponsor to provide responses to requests Evaluate and analyze data submitted by various parties to ensure it meets criteria set by the study protocol Monitor and update central database to ensure that all data is being process ti...
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This position reports into Head of Global Sourcing Area and works within Procurement across legal entities and national boundaries with a strong focus on procurement strategy and service delivery. This position would provide contract support within a therapeutic or division specialty. This position will also support the identification, selection, and management of suppliers and contracts across th...
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