Principal Clinical Data Manager

Accountabilities

• Lead and oversee all clinical data management activities across multiple complex global clinical studies and programs from start-up through database lock and study closeout.
• Provide strategic and technical leadership to ensure data management deliverables are completed accurately, efficiently, and in accordance with sponsor expectations, regulatory requirements, and project timelines.
• Act as the primary data management subject matter expert, offering guidance on study design, database development, data review processes, and data quality strategies.
• Collaborate closely with cross-functional teams including clinical operations, biostatistics, programming, medical monitoring, and regulatory stakeholders to support successful study execution.
• Monitor project progress, identify risks, and implement proactive solutions to maintain quality and timelines.
• Mentor and support data management team members, promoting professional development and best practices across the department.
• Participate in departmental initiatives focused on process improvement, operational efficiency, and innovation.
• Support business development activities by contributing to proposals, bid defenses, sponsor presentations, and project planning discussions.
• Participate in sponsor audits, regulatory inspections, and third-party reviews as required.
• Provide leadership support and act as a delegate for departmental management when necessary.

Requirements

• Bachelor’s degree or higher in Life Sciences, Biomedical Sciences, Computer Science, or a related discipline, or equivalent relevant professional experience.
• Minimum of 7 years of experience in clinical data management within the pharmaceutical, biotechnology, medical device, or clinical research industries.
• Extensive knowledge of clinical data management processes, industry standards, and regulatory requirements governing clinical trials.
• Advanced understanding of clinical trial documentation, including study protocols, case report forms (CRFs), statistical analysis plans, and clinical study reports.
• Demonstrated experience managing multiple complex clinical studies simultaneously in a global environment.
• Strong expertise in clinical data management systems, data review methodologies, and data quality assurance practices.
• Excellent analytical and problem-solving abilities with a proactive approach to issue resolution.
• Proven ability to work independently while maintaining oversight of multiple projects and priorities.
• Strong leadership, mentoring, and stakeholder management capabilities.
• Outstanding written and verbal communication skills with the ability to collaborate effectively across multidisciplinary teams.
• Exceptional attention to detail and commitment to delivering high-quality results.

Benefits

• Fully remote working opportunity with flexibility to work from the United Kingdom.
• Competitive salary package based on experience, qualifications, and market benchmarks.
• Comprehensive benefits package tailored to location and employment requirements.
• Opportunity to work on impactful global clinical research programs that contribute to advancing patient care and treatment development.
• Collaborative and inclusive work environment that values innovation, diversity, and professional growth.
• Access to experienced leadership teams and cross-functional experts across multiple disciplines.
• Ongoing professional development and career advancement opportunities.
• Exposure to complex, cutting-edge clinical studies and emerging therapeutic areas.
• Supportive culture focused on teamwork, knowledge sharing, and continuous improvement.
• Participation in a globally recognized organization committed to excellence in clinical research.

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