Clinical Data Manager Jobs in Vineland, NJ

The Senior Clinical Data Manager will oversee the Data Management team, coordinating data management activities across multiple projects to ensure efficient execution. This role involves managing clin...

The Principal Clinical Data Manager provides strategic leadership and oversight of clinical data management activities across multiple programs, ensuring high-quality data collection and compliance wi...

The Principal Clinical Data Manager is responsible for leading data management activities to ensure accuracy, consistency, and compliance with regulatory standards in clinical trials. This role involv...

The Senior Director of Clinical Data Management is responsible for overseeing all aspects of clinical data management across Immunocore's clinical trials. This strategic leadership role involves devel...

The Principal Clinical Data Manager provides strategic leadership and oversight of clinical data management activities across multiple programs, ensuring high-quality data collection and compliance wi...

The Senior Director, Clinical Data Management (CDM) is a strategic leadership role responsible for overseeing all aspects of clinical data management across all Immunocore clinical trials. Reporting t...

The Clinical Study Manager leads and oversees the operational planning and delivery of Phase I-IV clinical trials within specific countries, ensuring compliance with quality standards and regulations...

The Director of Data Management and Central Monitoring Reporting at Johnson & Johnson leads a team focused on the design and deployment of Clinical Data Central and Analytical Monitoring Analytics Too...

The Manager - Enterprise Data Management at ZS is responsible for overseeing program governance, business development, project delivery, and client management within the Digital & Technology practice...

The External Data Management Director is responsible for overseeing the management of external lab data throughout the clinical trial lifecycle, ensuring high-quality data handling and collaboration w...

The Senior Clinical Trial Technology Manager oversees oncology Imaging Vendors and provides program-level oversight to Clinical Technology suppliers. This role involves cross-functional collaboration...

The Clinical SAS Programmer is responsible for conducting high-quality statistical programming to support clinical development programs. This role involves generating datasets, tables, and figures, as...

The Validation Project Manager will plan, execute, and manage CQV projects while ensuring compliance with industry standards and regulations. This role involves collaborating with technical teams and...

The Associate Clinical Data Management Director oversees data management activities at the program level, ensuring quality and timely deliverables from study start-up to regulatory submission. This ro...

The CRM Program Manager at Penn Medicine is responsible for overseeing the use and adoption of CRM technology across various teams, providing strategic partnership and programmatic development. This r...

The Client Success Manager at ClinChoice is responsible for cultivating and leading relationships with clients in the Life Sciences sector, providing strategic counsel and driving growth across partne...

The Senior Clinical Research Associate (CRA) at ICON plc is responsible for overseeing and managing clinical trial activities to ensure compliance with protocols and regulatory requirements. This role...

The Director of Statistical Programming at AstraZeneca is responsible for leading and managing Programming teams, ensuring the quality of their deliverables, and contributing to the strategic initiati...

The Sr. Manager of Data Warehousing will oversee the design, development, and maintenance of the data warehouse environment, ensuring alignment with business objectives and compliance with regulatory...

The Senior QC Sample Data Management Specialist is responsible for managing sample and data processes within QC laboratories, including sample lifecycle tracking and ensuring compliance with GMP stand...

The Senior Director, Lead Statistical Programmer will lead multiple programming activities for Madrigal Pharmaceuticals, collaborating with biostatisticians and programmers to meet R&D objectives. Thi...

Capable of developing, executing, and assessing strategies to enhance processes and set direction in the TMF and Clinical Systems domain; proficient in identifying, understanding, and mitigating risks...

The Clinical Manager is responsible for overseeing the provision of quality patient care in a dialysis facility while ensuring compliance with regulatory requirements and operational policies. This ro...

The Senior Clinical Research Associate (CRA) or CRA II at ICON plc is responsible for overseeing and managing clinical trial activities to ensure compliance with protocols and regulatory requirements...

The Senior IRB Analyst assists the Director of Human Research Protections in ensuring compliance with federal and state regulations regarding the protection of human subjects. This role involves leadi...