Principal Clinical Data Manager in Canada Creek, Nova Scotia at Jobgether

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Principal Clinical Data Manager based in Canada.

This role offers an opportunity to provide senior-level clinical data management leadership across complex clinical research programs. You will oversee data management activities from study start-up through database lock, ensuring high standards of data quality, accuracy, and documentation. Working across mid-to-large and multi-study programs, you will lead teams of Clinical Data Managers and coordinate delivery against project requirements. The position combines hands-on expertise with program-level oversight, strategic guidance, and cross-functional collaboration. You will also help strengthen operational consistency, resource planning, and the adoption of data management best practices. As a senior subject matter expert, you will mentor colleagues and contribute to training initiatives across clinical research functions.

• Lead clinical data management activities from study start-up through database lock across paper-based and electronic data capture (EDC) studies.
• Take overall responsibility for data quality, documentation, and the successful delivery of data management activities for assigned clinical research projects.
• Manage mid-to-large, complex projects across a range of therapeutic indications and, when required, oversee multiple studies within the same client program.
• Lead teams of Clinical Data Managers and ensure contracted activities are delivered in accordance with applicable standard operating procedures and sponsor-specific requirements.
• Partner with Data Management leadership to promote consistent operations, efficient resource utilization, and the sharing of knowledge and best practices.
• Provide technical and project leadership, supporting teams in resolving challenges and achieving mutually agreed outcomes.
• Support the training and development of data managers on project-specific and general data management processes, procedures, and systems.
• Provide data management training and expertise to other functional teams when required.
• Act as a senior consultant and thought partner to management, providing guidance with a broader program and organizational perspective.

Requirements:

• Bachelor’s degree in a related field with 7+ years of relevant experience, including at least 5 years of clinical data management experience in a clinical research environment.
• At least 4 years of experience leading project teams.
• Thorough knowledge of ICH Good Clinical Practice (GCP) guidelines and other applicable regulatory requirements and standards.
• Strong understanding of medical terminology, clinical trials, and clinical research processes.
• Working knowledge of the CRO industry and its regulatory and operational relationship with pharmaceutical and biotechnology organizations.
• Demonstrated ability to lead by example and provide effective technical leadership and mentorship to team members.
• Strong consulting and influencing skills, with the ability to influence without authority and guide diverse project teams toward effective outcomes.
• Ability to think strategically and maintain a big-picture perspective while addressing project-level priorities.
• Expert-level proficiency with clinical trial databases and applications, such as IBM Clinical Development and Medidata RaveX, combined with the ability and willingness to learn new technologies.
• Strong understanding of project planning and project management methodologies.
• Excellent interpersonal, communication, organizational, and prioritization skills.
• Ability to work independently and collaboratively across multiple projects with different priorities.
• Strong mentoring capabilities and the ability to provide senior-level clinical data management expertise.

Benefits:

• Estimated hiring range of $114,000–$150,000 USD plus applicable bonus; compensation outside the USA varies according to local market data.
• Final compensation considers skills and experience, licensure and certifications, education, location, and current market conditions.
• Remote working opportunities.
• Flexible time off.
• Paid holidays.
• Medical insurance.
• Tuition reimbursement.
• Retirement plans.
• Opportunity to work within a global clinical research environment supporting life-changing therapies.
• Exposure to complex clinical research programs across diverse therapeutic areas.
• Inclusive and flexible work culture with a predominantly remote workforce.
• Opportunities to contribute to knowledge sharing, mentoring, and professional development.