This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Clinical Data Manager in Canada.

This role plays a critical part in ensuring the integrity, quality, and regulatory compliance of clinical trial data across multiple studies in a fast-paced, high-impact environment. You will oversee end-to-end data management activities from study start-up through database lock and study closeout, working closely with cross-functional teams and external vendors. Acting as the key point of contact for clinical data management, you will help ensure that data is accurate, complete, and delivered on time and within budget. The position involves hands-on leadership of EDC setup, CRF design, data validation, and quality oversight of CRO deliverables. You will also contribute to data review meetings, regulatory submissions, and study documentation processes. This is a contract opportunity within a mission-driven clinical organization focused on advancing innovative therapies in ocular disease.

In this role, you will lead clinical data management activities across assigned studies, ensuring compliance with regulatory standards and high-quality data delivery throughout the study lifecycle. You will act as the primary liaison for data management activities and oversee both internal and outsourced operations.

• Lead end-to-end clinical data management activities from study start-up to database lock and study closeout.
• Serve as the primary point of contact for all study-related data management communications.
• Oversee EDC build activities, including CRF design, edit checks, UAT, and system validation.
• Review and contribute to key study documents such as Data Management Plans, validation specifications, and data review plans.
• Ensure data quality through ongoing review, reconciliation, and issue resolution across study datasets.
• Manage CRO and vendor performance, ensuring timely and accurate delivery of data management outputs.
• Lead data review meetings and support regulatory submissions, CSR development, and database locks.
• Maintain TMF documentation and ensure proper archiving of clinical trial data and related records.

The ideal candidate brings strong clinical data management experience within pharmaceutical or CRO environments, with proven expertise in managing Phase I–III clinical trials and leading EDC systems and vendor operations.

• Bachelor’s degree in life sciences, computer science, or a related discipline.
• 5+ years of experience in Clinical Data Management (or 8+ years for senior-level profiles).
• Strong hands-on experience with EDC systems (e.g., Medidata Rave, Oracle InForm).
• Solid understanding of clinical trial processes, CDM standards, and regulatory requirements (ICH, FDA, GCP).
• Experience managing CRO vendors and overseeing outsourced data management activities.
• Familiarity with CDISC standards (CDASH, SDTM) and clinical data workflows.
• Strong analytical, problem-solving, and attention-to-detail skills.
• Excellent communication skills with the ability to collaborate across cross-functional teams.
• Ability to manage multiple priorities in a fast-paced clinical environment.

• Competitive hourly compensation ($70–$85/hour depending on experience).
• 6–12 month contract opportunity.
• Exposure to innovative clinical-stage programs in a mission-driven environment.
• Collaboration with experienced cross-functional clinical and scientific teams.
• Opportunity to work on end-to-end global clinical trials and regulatory submissions.
• Fast-paced environment with meaningful impact on data quality and trial outcomes.