Senior Clinical Data Manager

Warman O'Brien; Canada; Remote; CAD 90,000 - 120,000; Full time

Benefits offered by this job

Fully remote flexibility

Competitive salary

10% bonus

Collaborative environment

Opportunity for impactful work

Job summary

A leading pharmaceutical firm is seeking a Senior Lead Clinical Data Manager to drive data strategy and lead high-impact clinical projects fully remotely in Canada. The role requires extensive experience in data management, project leadership, and exceptional communication skills. You will oversee study execution, manage client relationships, and mentor junior team members, shaping the future of clinical development. This position offers competitive compensation and opportunities for professional advancement.

Qualifications

• 10+ years of Data Management experience, including 5-7 years leading clinical data projects.
• Proven track record of delivering full DM life cycles across multiple studies.
• Strong expertise in medical terminology, GCP, and regulatory expectations.

Responsibilities

• Lead end-to-end delivery of data management services across clinical projects.
• Serve as primary client partner for all DM deliverables.
• Provide strategic leadership in project planning and execution.

Skills

Data Management

Project Management

Communication

Client Management

Mentoring

Education

Bachelor’s degree in life sciences or related field

Job description

Senior Lead Clinical Data Manager | CRO - FSP | Remote – Canada | Permanent

Are you ready to take your Clinical Data Management expertise to the next level? Join us as a Senior Lead Clinical Data Manager and play a pivotal role in driving data strategy, innovation, and excellence across global clinical programs. This fully remote position offers the autonomy to lead high‑impact studies while partnering with world‑class teams and sponsors shaping the future of clinical development.

What you’ll be doing

• Lead the end‑to‑end delivery of data management services across complex, multi‑service clinical projects, ensuring quality, precision, and on‑time execution.
• Serve as the primary client partner for all DM deliverables, building strong relationships and guiding successful project outcomes.
• Provide strategic leadership in planning, execution, close‑out, milestone delivery, risk management, and communications.
• Act as Data Team Lead (DTL), Program Lead, or CDM Subject Matter Expert as needed.
• Mentor and develop junior team members, championing best practices and continuous learning.
• Support business growth through RFP participation, bid defences, and tailored solution design.
• Oversee multiple studies/programs from project planning to database lock and close‑out.
• Create and maintain Data Management Plans (DMPs) aligned with GCP, SOPs, and regulatory standards.
• Drive proactive quality oversight, issue management, and process improvement initiatives.
• Manage financial aspects including SOW/budget control, financial tracking, and invoicing.
• Collaborate with cross‑functional teams and external vendors on SAE reconciliation, lab/vendor data integration, and compliance activities.
• Represent the organization at industry conferences, workshops, and professional events.

What you’ll need

• Bachelor’s degree (or equivalent) in life sciences, health, biological, mathematical sciences, or a related field.
• 10+ years of Data Management experience, including 5‑7 years leading clinical data projects.
• A proven track record of delivering full DM life cycles across multiple studies and programs.
• Strong expertise in medical terminology, pharmacology, anatomy/physiology, GCP, and regulatory expectations.
• Exceptional communication, project management, and client‑facing skills.
• Experience negotiating with customers and managing change orders/out‑of‑scope activities.
• Ability to mentor, influence, and drive operational excellence within teams.

What’s in it for you

• Fully remote flexibility anywhere in Canada.
• Opportunity to lead high‑visibility global projects and work with top‑tier sponsors.
• A collaborative environment that values innovation, quality, and continuous improvement.
• The chance to make a meaningful impact in advancing clinical drug development.
• Competitive compensation, including a generous salary and 10% bonus.

What to do next

If this role aligns with your experience and ambitions, we’d love to hear from you.

Apply now with your CV and take the next step in your career.

Key Details

Seniority level: Mid‑Senior level | Employment type: Full‑time | Job function: Other | Industry: Pharmaceutical Manufacturing