- Merck & Co. (Rahway, NJ)
- …related study materials (eg, ICF documents / amendments); Partners with the Study Manager on study deliverables.Ensuring CRF design supports data ... Clinical Data, Clinical Operations, Clinical Outcomes, Clinical Research, Clinical Study Design, Clinical Testing, Clinical Trial… more
- Merck & Co. (Rahway, NJ)
- …operational/executional arms within the business.-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM) designs strategic ... - Responsible and accountable for establishing the timelines for clinical supply needs per study and providing...analyses , and/or develops mitigation strategies for review with clinical partners and senior leaders.- - Works… more
- Merck & Co. (Rahway, NJ)
- …Management Section of the GCS Planning organization. -Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates ... strategic and operational plans associated with the downstream activities of clinical supplies for their assigned studies . -The primary function of the IM CSPM… more
- Genmab (NJ)
- …and immunology experience preferredDemonstrated experience authoring protocols, investigator's brochures, and clinical study reports. Senior level candidates ... At Genmab, we are seeking a passionate and experienced Senior Medical Writing Manager to help us...of critical documents such as protocols, investigator's brochures, and clinical study reports.Contribute to Health Authority briefing… more
- Merck & Co. (Rahway, NJ)
- …teams and the operational/executional arms within the business.-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary ... effectively communicate with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong… more
- Eisai, Inc (Nutley, NJ)
- …Data Review programming and JReview within IODS. Reporting to the Assoc. Director of Clinical Programming is the senior level highly technical SAS and JReview ... Environment Implementation of new programs, enhancements & support of Eisai Clinical Computing Environment Support study migration, program validation, technical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary: The Senior Director, Head of RBQM (Risk Based Quality Monitoring) sets the vision ... Collaboration and partnership with other functions and stakeholders in supporting clinical trial monitoring and execution through RBQM activities. Accountable for… more
- Genmab (NJ)
- …decision making. Responsibilities in leading the programming efforts of at least one study are in scope.The Programming Manager will support the Data Management, ... Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above by...developing and writing corresponding SAS or other programs. The Senior Programming Manager may also serve as… more
- Merck & Co. (Rahway, NJ)
- …with senior cross-functional leadership to optimize efficiencies in the clinical development space. Preferred skills include experience in the application of AI, ... teams both as a direct manager and a second line manager (ie, managers of managers)Demonstrated collaboration with senior cross-functional leadership in… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Senior Manager , Clinical Data Standards, Bristol-Myers Squibb Company** ... + Good Clinical Trial (GCT) practice, + Regulatory requirements, + Clinical Data Interchange Standards Consortium (CDISC), Study Data Tabulation Model (CDISC… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … studies and ensures integrity and interpretation of study data of a clinical development program. The Senior Manager leads in a matrix environment as ... clinical studies and programs. As a Senior Manager in Oncology Clinical ...in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical… more
- Bristol Myers Squibb (Princeton, NJ)
- …Myers Squibb's mission to advance clinical development through data-driven innovation, the Senior Manager - Analytical AI in Clinical Development will ... and optimize end-to-end pipelines that address critical business problems in clinical study design and execution. + Automate workflows to process and analyze… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** As Senior Clinical Data Manager , you will be responsible for performing end-to-end Data Management activities for assigned ... studies . You will ensure that clinical study data is collected, processed, and validated in a consistent and appropriate manner according to BD's QMS… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …onsite position in one of our office locations. Fully remote is not eligible._ The ** Senior Clinical Study Lead** (CSL) is expected to operate with ... trials from study design, through execution, to study close out. The Senior CSL is...studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Senior Manager , CDM oversees lead Data Managers across clinical studies in specific therapeutic areas to ensure timely and high-quality data ... recruitment, development, and performance. **As a Senior Manager , a typical day may include:** ** Study ...: + Serve as the primary DM contact for clinical teams, CROs, and external vendors. + Oversee all… more
- Taiho Oncology (Princeton, NJ)
- …to transforming the landscape of cancer treatment and improving patients' lives. As a Senior Manager , Clinical Research Scientist, you will play a pivotal ... at the forefront of cancer research. Position Summary: The Senior Manager , Clinical Research Scientist...of relevant high-quality clinical documents such as study protocols and clinical study … more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- As a Sr. Manager Global Procurement-R&D you will be responsible to support and assist in the development and implementation of the Clinical Category Management ... is required to have a Bachelor's degree in a relevant field of study plus relevant, progressive experience in procurement, including experience in the Pharmaceutical… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …manage and close-out clinical studies , including involvement in authoring clinical study process improvements and SOPs. + Meets all requirements for ... Senior Clinical Trial Manager (...Senior Clinical Trial Manager ( Senior CTM)... studies . + Proven ability to effectively author clinical study and regulatory documentation. + Ability… more
- Merck (Rahway, NJ)
- …and related study materials (eg, ICF documents / amendments); Partners with the Study Manager on study deliverables. + Ensuring CRF design supports data ... Clinical Data, Clinical Operations, Clinical Outcomes, Clinical Research, Clinical Study Design, Clinical Testing, Clinical Trial… more
- Merck (Rahway, NJ)
- …the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and ... operational plans for all activities associated with clinical supplies for their assigned studies , which...+ Responsible and accountable for establishing the timelines for clinical supply needs per study and providing… more
