- IQVIA (Parsippany, NJ)
- …Project Management Director/Trial Delivery Manager (TDM) to lead and coordinate global and regional clinical trial management activities. This role ensures the ... contact for country and regional staff and internal teams. + Partner with Global Trial Leads to oversee central trial activities from start-up to close-out. +… more
- Sanofi Group (Morristown, NJ)
- …and co-creating tailored solutions to meet those needs. We are an innovative global healthcare company with a focus on immunology that extends to innovation in ... or within the patient community, including medical-led T1D screening events per global standards + Execute local congress plans including medical-led T1D screening… more
- AECOM (Piscataway, NJ)
- …to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and ... projects that create a positive and tangible impact around the world. We're one global team driven by our common purpose to deliver a better world. Join us.… more
- Coinbase (Trenton, NJ)
- …day, as we build the emerging onchain platform - and with it, the future global financial system. To achieve our mission, we're seeking a very specific candidate. We ... walkthroughs, testing, deficiency remediation, and report writing in accordance with regulatory requirements, you'll play a key role in strengthening our position… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …Ensuring independent quality oversight of Clinical and Post-Marketing Safety, Regulatory Affairs, and Medical Affairs activities throughout the product lifecycle. ... overseeing the quality of Non-Clinical, Product Development, Clinical, Patient Safety, Regulatory Affairs, and Medical Affairs activities. + Evaluate the compliance… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …within NCSVS. The role is critical to ensuring the integrity, security, and regulatory compliance of data systems used in support of drug development, nonclinical ... ideal candidate will have a strong background in laboratory informatics, regulatory compliance, and electronic data integrity principles. Operating within a matrixed… more
- Bristol Myers Squibb (Princeton, NJ)
- …+ Apply expertise in LIMS, ELN, and clinical data management systems to support regulatory submissions and study execution. Project & CRO Management + Act as the ... ICH-GCP, and GLP standards. + Support internal/external audits and regulatory submissions (CDx, LDT, IVDR filings). Cross-Functional Collaboration + Collaborate… more
- IQVIA (Parsippany, NJ)
- …and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to ... compliance and data integrity. + Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution… more
- JPMorgan Chase (Jersey City, NJ)
- …and enhance industry compliance. As a Tech Risk & Controls Director in Global Technology Standards & Control Objectives organization, you will play a pivotal role ... will be crucial in ensuring the firm's adherence to regulatory obligations and industry best practices. Your work will...strength and the diverse talents they bring to our global workforce are directly linked to our success. We… more
- TD Bank (Mount Laurel, NJ)
- …Provides strategic direction on a broad and diverse range of complex global Risk program activities + Develops Risk enterprise-wide frameworks, policies, standards, ... proactive strategies, tactics, policies and programs to effectively manage regulatory /compliance issues + Contributes to the development and implementation of… more
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