Clinical Research Associate Manager

SummaryAs a Clinical Research Associate Manager, you’ll empower and guide a team of CRAs to deliver high-quality, compliant, and timely trial execution. Your influence will drive recruitment strategies, ensure monitoring excellence, and foster a culture of integrity and innovation. If you're passionate about mentoring talent, making a meaningful impact in clinical trials, and stepping into a local leadership role where your expertise in clinical research will directly shape the future of global drug development, this is your opportunity to lead with purpose.About The RoleLocation: Amsterdam, NetherlandsKey ResponsibilitiesLead hiring, training, and retention of CRAs for Phase I–IV global clinical trialsSupport recruitment strategies and site performance in collaboration with Clinical Project ManagersEnsure monitoring quality, timely data entry, and resolution of trial-related issuesIdentify and resolve CRA competency gaps through targeted training and co-monitoring visitsPromote compliance culture and uphold ethical standards in trial executionManage CRA performance and implement development and improvement plansCoach CRAs on risk-based monitoring processes and related systemsExecute annual CRA oversight visits to assess competency and resolve issuesCollaborate with CPMs to address monitoring trends and training needsEnsure adherence to clinical data standards, GCP, SOPs, and regulatory requirementsSupports Clinical Development Audits, site audits and inspection and ensures CAPA follow-up and implementation for CRA and site identified issuesDevelop and implement local monitoring resource strategyEssential RequirementsMinimum 7 years of experience in clinical research, including planning and monitoring clinical trialsProven leadership in project management and team development within clinical operationsStrong understanding of clinical drug development and trial execution processesExcellent communication and relationship-building skills with internal and external stakeholders along with strong presentation skills.Proficiency in digital tools and technology relevant to clinical trial managementFluency in Dutch is required for this role, in addition to EnglishDesirable RequirementsExperience with risk-based monitoring strategies and implementation in global clinical trialsAbility to travel domestically for site visits, training, and meetingsCommitment To Diversity And InclusionNovartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-cultureJoin our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/networkBenefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards