Clinical Data Manager

Adecco is currently hiring a Clinical Data Manager for a 1-year opportunity with a leading medical device and healthcare technology organization in Ottawa, ON . This role is ideal for professionals with experience in clinical data management, clinical trials, electronic data capture (EDC), clinical research, CTMS, GCP compliance, and clinical database management.

As a Clinical Data Manager, you will support all phases of clinical studies, from study start-up through close-out, ensuring clinical data is collected, validated, and maintained in compliance with regulatory requirements and industry standards. You will play a critical role in delivering accurate, high-quality databases that support statistical analysis and clinical decision-making.

• Pay Rate: $96,000-$110,000/year
• Location: Ottawa, ON | Travel up to 5% within Canada and the United States
• Job type: Temporary 1 year | Full-time
• Vacancy Status: This posting is for an existing vacancy .

Here's why you should apply:

• Paid weekly accurate and on time
• Strong health and safety programs
• Medical and dental benefits once qualified
• Free training programs
• New and quicker onboarding process

Responsibilities:

Clinical Data Management

• Design, develop, and maintain Electronic Data Capture (EDC) systems and clinical study databases.
• Create and maintain case report forms (CRFs), validation rules, and edit checks.
• Perform data review, cleaning, and validation activities to ensure accuracy, completeness, and consistency.
• Investigate data discrepancies, missing information, and query resolutions.

Clinical Trial Support

• Support data management activities throughout study start-up, conduct, and closeout.
• Maintain study documentation, data management files, and archival records.
• Generate reports and data review tools for clinical monitors and study teams.
• Collaborate with clinical operations, biostatistics, and project teams to support study objectives.

Compliance & Quality

• Ensure compliance with study protocols, GCP guidelines, regulatory requirements, and company procedures.
• Support implementation and maintenance of FDA 21 CFR Part 11 compliant systems.
• Participate in quality control and quality assurance activities.
• Assist with corrective actions and continuous process improvements.

Training & Project Support

• Train investigative sites and study team members on data management processes and systems.
• Participate in investigator meetings and support study-related training activities.
• Support EDC and CTMS implementation, optimization, and user adoption initiatives.
• Contribute to project planning, timelines, and study deliverables.

Qualifications and Skills:

• Bachelor’s degree in health sciences, Clinical Research, Biological Sciences, Medical Technology, or a related field.
• Minimum 6 years of experience in Clinical Data Management, Clinical Research, Clinical Trials, EDC, or CTMS environments.
• Strong understanding of Clinical Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS).
• Knowledge of ICH-GCP, clinical trial regulations, and FDA 21 CFR Part 11 requirements.
• Experience designing databases, CRFs, validation checks, and data review processes.
• Strong project coordination, planning, and prioritization skills.
• Excellent written and verbal communication abilities.
• Medical Technology, Clinical Laboratory, Diagnostics, or In-Vitro Diagnostics (IVD) experience.
• Experience interpreting laboratory results and clinical data.
• Experience implementing EDC or CTMS solutions for clinical studies.
• Experience supporting regulated healthcare or medical device environments.
• Must be legally eligible to work, and reside in Canada