Clinical Trial Manager Jobs in New Brunswick, NJ

Champion the clinical operations team, ensuring project success through resource management, process efficiencies, and compliance. Drive training, metrics development, and mentorship to enhance team c...

Unlock potential by leading regulatory CMC strategies for oncology products, coordinating submissions, and collaborating across teams to ensure compliance and successful product registration in a dyna...

Transform global pharmacovigilance operations by overseeing clinical trial safety, vendor management, and ensuring compliance. Collaborate with cross-functional teams to enhance patient safety and mai...

Unlock your potential as a key leader in GxP auditing, driving compliance and quality oversight across computerized systems in regulated environments. Collaborate cross-functionally to enhance risk ma...

Innovate with us by shaping and operationalizing governance for agentic AI technologies. Collaborate with diverse teams to ensure responsible, compliant AI use at scale while advancing innovative solu...

Unlock potential by enhancing our research operations through effective management of core systems, improving team collaboration and organizational structures while ensuring seamless support for resea...

Engage in leading global project management activities for clinical drug development, ensuring alignment with strategic objectives through cross-functional collaboration, risk management, and process...

Elevate project outcomes as you lead global deliverable management for a complex multi-country initiative, ensuring compliance and operational success across teams and milestones while fostering colla...

Join a dynamic team focused on ensuring compliance and performance for clinical research sites. Develop strong relationships with stakeholders while overseeing study conduct and site management across...

Grow your career with a pivotal role in clinical research site management, ensuring compliance, performance, and relationships. Drive local expansion and contribute to the improvement of study protoco...

Lead clinical research by managing site compliance and performance across protocols. Develop strong site relationships, conduct monitoring activities, and ensure adherence to regulations while expandi...

Elevate user success with Veeva CRM and Salesforce by delivering engaging training, comprehensive support, and effective communication strategies, ensuring teams maximize CRM capabilities and experien...

Grow your career with strategic leadership in clinical partnerships and feasibility assessments, overseeing vendor relations and cross-functional initiatives to ensure successful study execution and o...

Drive strategic product management and governance for advanced eSource platforms, ensuring compliance and enhancing decentralized and hybrid trials. Collaborate cross-functionally to shape product vis...

Empower strategic alliances by driving growth and adoption for our largest CRO partners. Build influential relationships while navigating high-stakes negotiations to maximize our platform's impact and...

Help us shape the future of clinical trials by providing regulatory guidance and maintaining compliance. Collaborate within cross-functional teams to ensure successful submissions and uphold industry...

Unlock potential in regulatory affairs by steering clinical trial submissions, ensuring compliance and strategic oversight. Collaborate with project teams, advising on regulatory pathways for successf...

Drive client negotiations and deal strategies, ensuring alignment with company goals. Collaborate closely with sales to translate complex offerings into optimized deal structures, fostering successful...

Join a dynamic data science team to innovate and deliver impactful clinical trial insights. Lead cross-functional initiatives while developing talent and optimizing processes to elevate performance an...

Lead the development and continuous enhancement of a site-wide GMP training program, ensuring compliance and effectiveness while serving as the SME during inspections and audits. Collaborate on global...

Shape the future of Clinical Quality Assurance by leading strategic compliance initiatives, ensuring adherence to GCP and GVP regulations, and enhancing risk management and inspection readiness across...

Shape the future of oncology therapeutics by driving global regulatory strategy and enabling fast track approvals for novel drug candidates. Collaborate cross-functionally to ensure compliance with FD...

Join a team that drives innovation in drug development by supporting project managers in maintaining timelines and budgets across a diverse portfolio of R&D programs, ensuring operational excellence a...

Join us to drive biosimilar programs from development to regulatory approval. As a pivotal Project Manager, you will streamline workflows, enhance collaboration, and ensure data integrity to support o...

Drive effective governance by prioritizing agendas for senior leadership forums, ensuring strategic focus, and facilitating impactful discussions that lead to clear, actionable decisions, ultimately o...