73 Clinical Trial Data Management Jobs in East Brunswick, NJ
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Senior Director, Clinical Development (exclusive) Adecco - Elizabeth, NJ, United States for assigned clinical trials/programs (phase I - III). Develop protocols/amendments, provide medical monitoring of study conduct and oversight of patient safety, and provide medical support for data analysis 2 days ago
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Clinical Data Analyst Smart IT Frame LLC - , NY, United States with Tableau • Understanding of clinical trial data management systems, REDCap preferred • Knowledge of statistical analysis techniques and software such as R • Programming skills, Python preferred • Experience Yesterday
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Clinical Trial Specialist at Vitalief Vitalief - New Brunswick, New Jersey supervision of the Nurse Manager of Clinical Research Center, performs patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, data management. and other clinical trial 9 days ago
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***Sr. Clinical Programmer Analyst*** || ***100% Remote*** Vaco - Trenton, NJ, United States and presentation skills Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC. Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical 4 days ago
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Clinical Trial Associate i-Pharm Consulting - Pennington, NJ, United States management systems and safety databases is a plus. Experience working on international clinical trials and interacting with IRBs. SOP development experience. Training experience for new and existing employees 7 days ago
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Associate Digital Product Manager, Clinical Development Genmab - Princeton, New Jersey in Development Operations, including Trial Management, Trial Monitoring, Clinical Data Management, Trial Analytics, Stats Programming, and Medical Writing . These digital products are crucial to enable Business 3 days ago
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Clinical Trial Business Operations Specialist Planet Pharma - Lawrenceville, NJ, United States clinical trial data / clinical trial performance metrics Ability to summarize complex data Ability to identify trends, risk and issues in data Highly effective written and verbal communication 9 days ago
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Associate Principal Scientist Pyramid Consulting, Inc - Rahway, NJ, United States , data analysis and interpretation) of COA/PRO development, validation, electronic migration and interpretation into clinical trial and observational studies. Ability to understand and respond to multiple 14 days ago
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Senior Local Trial Manager - Immunology (1 of 3) Johnson and Johnson - Raritan, NJ . LTM) is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. The Senior Local Trial Manager (Sr. LTM) is the primary point 2 days ago
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Sr. Medical Director- 602116 Planet Pharma - New York, NY, United States and/ or escalation of reported safety data in terms of trial endpoints, pause criteria and/ or Safety Data committees such as a DSMB, Protocol Safety Review Team (PSRT), Independent Data Monitoring Committee (IDMC 10 days ago
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