[Remote] Principal Clinical Data Manager - US/Europe - Remote

Note: The job is a remote job and is open to candidates in USA. Worldwide Clinical Trials is a global, midsize CRO committed to improving lives through innovative clinical research. The Principal Clinical Data Manager will oversee and manage complex data management projects, ensuring accuracy and timely delivery of data for regulatory submissions while providing mentorship and support to the team.ResponsibilitiesOversee, lead, manage and provide technical expertise within the assigned complex projects/programs to ensure that they are executed in an efficient, accurate and timely manner to the Sponsor’s satisfaction. Provide subject matter expert support, solution management and departmental support for project initiatives and trainingProvide fully independent and autonomous leadership of data management services (start up, conduct and close out) across multiple complex global projects/programsLiaise with DM Management at regular intervals to discuss progress and any issues outstanding (e.g. during Project Review Meetings)Collaborate with internal WCT departments working on the same project Provide mentorship to other members of the DM departmentParticipate in and co-lead departmental initiatives for process improvement and efficiencies as defined by the DM Departmental leadershipDeputise for Manager, DM as requiredTo provide support to Business Development staff by participating in preparation of proposals and presentations to sponsorsTo participate as necessary in sponsor audits, regulatory authority inspections and other third party meetingsSkillsExcellent attention to detailExcellent written and verbal communication skillsExpert knowledge of data management best practices & technologies as applied to clinical trialsExcellent communication and interpersonal skills to collaborate with cross-functional internal and external teamsAdvanced understanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processesStrong independent analytical and problem solving skillsIndependent and autonomous project oversight skillsBachelor's degree or higher in biomedical sciences, life sciences, computer science or related discipline — or equivalent relevant experienceMin of 7 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industriesBenefitsIn addition to base salary, we offer a competitive benefits package depending on location.Company OverviewWorldwide Clinical Trials is a global CRO that provides preclinical and Phase I-IV clinical development services to pharmaceutical industry. It was founded in 1986, and is headquartered in Morrisville, North Carolina, USA, with a workforce of 1001-5000 employees. Its website is https://www.worldwide.com.Company H1B SponsorshipWorldwide Clinical Trials has a track record of offering H1B sponsorships, with 1 in 2024, 5 in 2023, 3 in 2022, 2 in 2021, 2 in 2020. Please note that this does not guarantee sponsorship for this specific role.