Principal Data Manager I

About Our Client:The organization is a full-service contract research organization (CRO) that provides clinical research services to pharmaceutical, biotechnology, and medical device industries worldwide. It focuses on addressing challenges in clinical trial data management, offering expertise in statistical and data management to support the development of advanced drugs, biologics, and medical devices. Established in 2004, the organization operates globally with headquarters in Canada and the US and additional offices in Asia and Europe. It is recognized for high-quality deliverables, customer service, and flexibility. About the Opportunity:The PRINCIPAL DATA MANAGER I is responsible for leading data management activities to ensure accuracy, compliance, and timely delivery of clinical trial data. This role acts as the primary contact for data management communication and oversight, providing technical and procedural guidance. It contributes by validating data, managing database design and modifications, facilitating training, and coordinating project tracking, thereby supporting successful clinical trial execution and data integrity. Responsibilities:Serve as primary contact for data management timelines, deliverables, and issue resolution.Perform and oversee data management tasks including database design, test planning, and data transfer specifications.Review and resolve data queries from multiple sources.Manage non-Case Report Form data management activities.Plan and execute data processing ensuring compliance with sponsor requirements.Validate electronic data and generate study monitoring reports.Review and develop database edit check specifications.Provide training on electronic data capture systems and quality control processes.Participate in project meetings and assist with resource planning.Manage database modifications post go-live.Develop and maintain Data Management and Data Quality Review Plans.Assist in clinical data standards development and departmental improvement initiatives.Support project bidding, billing, and milestone tracking.Monitor regulatory requirements and industry best practices.Cooperate with Quality Assurance on audits.Ensure proper archival of data management documentation. Requirements:M.Sc. or B.Sc. in a related field.Ten years of related clinical data management experience.In-depth knowledge of clinical trial data management concepts, procedures, and relevant regulations. Pay Range and Compensation Package:The pay range and compensation package for this role will be determined based on the candidate's experience, skills, and other relevant factors. Equal Opportunity Statement: Our client is an equal opportunity employer. They celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, or national origin. Note:RemoteHunter is a recruitment partner of this role. Please note that all employment decisions, including candidate assessment, interviews, hiring, compensation, and employment terms, are made exclusively by the hiring employer.