When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Make a Meaningful Impact — Join Parexel as a Data Manager II We are seeking a highly skilled and experienced Data Manager II to join our global team at Parexel. In this pivotal role, you’ll provide technical expertise across all aspects of Data Management in clinical trials, ensuring the delivery of high-quality, timely data that supports life-saving research. As the single point of contact for Data Management deliverables, you’ll collaborate cross-functionally with Clinical, Biostatistics, Database Programming, Medical, and Medical Writing teams. This is a fast-paced, dynamic position ideal for someone who thrives under pressure, communicates clearly, and brings a proactive, solutions-driven mindset. You’ll lead 2–3 studies depending on scope, working closely with a cross-functional team including the Delivery Lead, Clinical Operations Lead, and a small team of Clinical Data Analysts/Coordinators. If you're passionate about advancing healthcare and want to be part of a team that puts patients first, this is your opportunity to make a meaningful impact. Job Title: Data Manager II Location: Remote (Canada Based) Department: Data Management Employment Type: Full-Time Time Zone: Flexible working hours Key Responsibilities Study Oversight & Delivery Lead Data Management activities from database setup through study close-out. Manage timelines for Go-Live, Interim Deliveries, and Final Database Lock. Coordinate integration of ancillary systems and ensure data flow efficiency. Identify risks, define mitigations, and drive resolution with stakeholders. Monitor study metrics and provide insights on study health and trends. Serve as the functional lead, facing the sponsor and managing expectations. Client Engagement & Proposals Represent Parexel’s technical and operational capabilities during bid pursuits. Contribute to proposal development and present confidently to sponsors. Quality & Compliance Ensure adherence to SOPs, ICH/GCP guidelines, and regulatory requirements. Maintain inspection-ready Trial Master File. Support audits and inspections; drive corrective/preventive actions. Financial & Resource Management Collaborate on project resourcing and staff assignments. Understand project budgeting and scope management. Monitor and resolve project variances, including scope changes. Training & Development Deliver project-specific and on-the-job training. Maintain training compliance and support team development. Company Initiatives Provide functional input on company-wide initiatives. Ensure accurate data entry in management systems. Systems & Tools Medidata Rave (required experience) Veeva Vault EDC (nice to have) Familiarity with other clinical trial systems (e.g., InForm, DataLabs) Required Skills & Competencies 2–3 years of experience as a DM Lead in a CRO, managing fast-paced studies. Proven leadership in global, cross-functional teams. Strong negotiation and influencing skills. Excellent communication skills — clear, calm, and confident. High adaptability and problem-solving capabilities. Ability to manage conflicts and remain composed under pressure. Strong customer focus and commitment to quality. Proactive, driven, and flexible — able to thrive in dynamic environments. Effective time management and prioritization. Ability to travel as required. Qualifications Bachelor’s degree in a science or clinical-related field. Extensive experience in the clinical research industry. Strong knowledge of clinical trial systems (e.g., Rave, Veeva, InForm). Familiarity with SDTM/CDISC/CDASH standards. Understanding of project financials, forecasting, and scope management. Fluency in written and spoken English. Why Parexel? At Parexel, you’ll be part of a purpose-driven organization that puts patients first. We offer flexible work arrangements, a supportive team culture, and opportunities to grow your career while making a real difference in global healthcare. Ready to lead with heart? We’re open to interviewing and excited to consider candidates who bring the right attitude and experience. Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.
