- Taiho Oncology (Princeton, NJ)
- … operations practices and processes ensuring consistent delivery across studies . Education/Certification Requirements: + Associate 's degree or equivalent. ... impactful results. The leadership and support provided by our Clinical Operations team are the cornerstone of...dynamic team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for… more
- Bristol Myers Squibb (Princeton, NJ)
- …aspects of study design. + In collaboration with Medical Writing and Clinical Operations , prepares study protocols, amendments, specific sections of ... to, collaboration on functional area activities during program implementation, clinical study start-up/execution/close out, data analysis/reporting, and… more
- Vitalief (New Brunswick, NJ)
- …performance and trial outcomes. + Innovation-Driven: Operate at the intersection of clinical research, financial operations , and advanced technology to transform ... thought leadership forums. Required Qualifications: + 8+ years of experience in clinical research operations , financial management, or related roles. +… more
- Bristol Myers Squibb (Princeton, NJ)
- …your application should be directed to Chat with Ripley. R1598215 : Associate Director - Incentive Compensation- Field Operations **Company:** Bristol-Myers ... careers.bms.com/working-with-us . **Summary:** Reporting into the Commercialization Strategy & Operations group, the Field Incentive Compensation role plays a… more
- Bristol Myers Squibb (Madison, NJ)
- …& completeness of all data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database lock. **Position Summary** The Senior ... BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, ...not limited to: **Project Management and Leadership** + Provides clinical data management leadership within the study … more
- AbbVie (Florham Park, NJ)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director, Statistics provides statistical leadership for clinical ... of methodologies for confounding control and bias minimization in observational studies preferred. Key Stakeholders Clinical development experts Statistical… more
- Bristol Myers Squibb (Madison, NJ)
- …effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback ... TA, where deemed necessary. + Provide quality and compliance consultation to clinical trials teams throughout study lifecycle. + Provide regulatory intelligence… more
- AbbVie (Florham Park, NJ)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director, Statistics - Immunology provides statistical leadership for ... clinical development and life-cycle management strategies for assigned projects....trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple… more
- Ascendis Pharma (Princeton, NJ)
- …groups. + Work with internal stakeholders including Commercial, Legal, Regulatory, Clinical Development, Clinical Operations , Compliance, Pharmacovigilance, ... member of the Endocrine Medical Sciences team for the US business, the Associate Medical Director supports the US Medical Director for deliverables and activities… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …maintain the effectiveness of the Otsuka Quality Systems that support OPDC-sponsored clinical studies as well as drive continuous improvement. **Job ... release process for OAPI GMP release of Contract Manufacturers operations supporting clinical and commercial products. +...escalation of any situations with potential negative impacts on clinical study supplies, supply chain for commercial… more
- Sanofi Group (Morristown, NJ)
- …ISO standards (13485, 15189), CLIA accreditation, lab developed test, and clinical performance studies .Ability to synthesize and critically analyze data ... **Job Title:** GRA Device Associate **Location:** Cambridge, MA/ Morristown, NJ/ Washington DC...Our department bridges the gap between technical development, manufacturing operations , and global regulatory authorities to ensure compliance while… more
- ThermoFisher Scientific (Bridgewater, NJ)
- …Office **Job Description** PPD is revolutionizing patient recruitment. As the clinical research division of Thermo Fisher Scientific, PPD has launched Patient ... enabled solutions, Patient First optimizes patient recruitment and engagement, site operations , and quality data collection. Step into a high-impact role where… more
- Bristol Myers Squibb (Princeton, NJ)
- …and outcomes. + Coordinate GLP-compliant bioanalytical programs (PK/PD/ADA) supporting clinical studies ; oversee assay timelines, critical reagents, data ... focus on Companion Diagnostics (CDx) design control, validation, and clinical enablement, and the agility to pivot to GLP...CLIA/CAP, IVDR, ISO13485, and 21 CFR 11 across lab operations , data, and vendor ecosystems - so we are… more
- Bristol Myers Squibb (Madison, NJ)
- …to lead structured benefit-risk assessments for assigned assets from early clinical development through late-stage and post-marketing. This role requires close ... relevant departments across the organization, including medical safety assessment, clinical development, global regulatory, epidemiology and others. The SBRA Lead… more
- Bristol Myers Squibb (Princeton, NJ)
- … Overview for Type II variation and coordinate expert reports. + Provide clinical trial expertise for existing evidence generation studies or health-authority ... Read more: careers.bms.com/working-with-us . **Position Summary:** The Established Brands Associate Director, Medical Affairs, is responsible for leading and… more
- Merck (Rahway, NJ)
- …include research and development, analytical, regulatory, quality, packaging, and operations at our commercialization and commercial supply sites. We recognize ... **Key Responsibilities:** + Plan, conduct, and interpret pharmaceutical process development studies with manager and team support, such as scale up, technology… more
- Merck (Rahway, NJ)
- …ICD-10-CM, SNOMED, LOINC, NDC, HCPCS, and CPT. + Experience in developing study protocols for non-interventional and methodological research studies , including ... **Job Description:** We are seeking a highly skilled and motivated Associate Principal Scientist/ Associate Director with expertise in conducting outcome… more
- BeOne Medicines (Pennington, NJ)
- …root cause analysis, and risk management. + Experience with tech transfer to clinical /commercial manufacturing facilities. + Knowledge of study design such as ... and authoring of various reports. This position reports directly into the Associate Director, Manufacturing Science and Technology (MST) Cell Culture and is located… more
- Bristol Myers Squibb (New Brunswick, NJ)
- … is responsible for the supply of drug product administered to patients in clinical studies worldwide. In Global Product Development and Supply the team works ... state and local regulations. **EDUCATION REQUIREMENTS** **:** + Two year Associate Degree in Science related to Pharmaceutical Development plus specialized… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …life-threatening diseases worldwide. Headquartered in Foster City, CA, Gilead has operations in North America, Europe, Asia, and Australia. For more information, ... exciting opportunity within the US Medical Affairs (USMA) organization for an Associate Director within Oncology Medical Strategy. Reporting to Executive Director of… more