Closed listing
Director - Medical Information
- Canada
Contract
This opening has closed.
The original listing is kept below for reference.
Job details
- Job type
- Contract
- Posting language
- English
- Posted
Similar jobs hiring now
Search current openingsOriginal job description
Archived listing. The details below describe a past opening.
We are seeking a Director, Medical Information to support the delivery and continued evolution of our Medical Information services. This role will be responsible for providing strategic oversight of sponsor accounts, ensuring high-quality and compliant MI operations, and contributing to process excellence and functional growth within a growing organisation.
The position offers the opportunity to work closely with leadership, cross-functional teams, and clients, while helping shape scalable and efficient ways of working across the MI function.
Why this matters for you:
This role is ideal for someone looking to take on broad operational responsibility and contribute beyond day-to- day delivery.
In this role, you will:
- Provide strategic oversight of sponsor accounts with end-to-end accountability for Medical Information activities
- Drive team growth, capability development, and operational excellence
- Lead process improvements, SOP development, and technology-enabled solutions
- Partner with internal stakeholders during program planning and business discussions
- Apply your Pharmacovigilance (PV) experience to support effective collaboration across MI and PV activities
What you will own:
Service delivery and client ownership
- Lead end-to-end MI delivery for assigned sponsor clients, ensuring adherence to contractual SLAs, applicable regulations, and global guidance
- Act as the primary point of accountability for quality, timelines, and compliance across your portfolio
- Handle and oversee medical enquiries from HCPs, patients, consumers, and other stakeholders across phone, email, and other channels, including non-IST coverage where required
- Own quality control of MI responses, escalations, and adverse event and product complaint handoffs to PV and Quality
Function building and team leadership
- Lead and mentor a growing MI team, with a clear mandate to scale and shape the function
- Recruit, onboard, coach, and develop MI Associates and Specialists
- Identify skill gaps, design training plans, and elevate the technical and scientific capability of the team
- Oversee workload distribution and proactively escalate risks before they impact quality or delivery
Content, systems, and continuous improvement
- Author and review SOPs, work instructions, and controlled documents for the MI function
- Lead development and lifecycle management of Standard Response Documents, FAQs, and global content libraries
- Oversee MI project setup, database configuration, validation, and onboarding for new client engagements
- Contribute to how we use technology, automation, and AI to make MI delivery faster and better, without compromising scientific rigour
Compliance, audits, and stakeholder engagement
- Represent the MI function during sponsor audits, regulatory inspections, and internal quality reviews
- Maintain a strong compliance posture across documentation, training, and CAPA
- Partner with PV, Quality, Regulatory, and Commercial teams internally, and with sponsor Medical Affairs counterparts externally
What we are looking for:
Experience
- 15+ years in life sciences, with demonstrable depth in Medical Information, Pharmacovigilance, or a combination of both
- Prior MI management or MI team-lead exposure in a CRO, pharma, or biotech setting
- Track record of managing client relationships, SLAs, and audit readiness, ideally across multiple sponsors or therapy areas
- Experience handling medical enquiries across global markets and time zones
Skills and qualifications
- Life sciences or pharmacy degree; PharmD, MPharm, or equivalent advanced qualification preferred
- Strong working knowledge of MI and PV regulations, ICH guidelines, and global pharmacovigilance frameworks
- Comfortable authoring SOPs and controlled documentation
- Hands-on familiarity with MI databases and content management systems
How you operate
- You take ownership and do not wait to be told what to escalate
- You hold a quality bar without becoming a bottleneck
- You can coach a junior associate one hour and brief a sponsor lead the next
- You are curious about where the function is going, not just how it runs today
What we offer
- A clear and visible leadership career path, with continued growth opportunities as the function expands
- Direct exposure to leadership, clients, and the commercial side of the business
- The opportunity to build and shape a team rather than simply maintain one
- Competitive compensation, with structured performance reviews and growth planning
- Flexibility on working arrangements where the role permits
More about this job
Responsibilities
Lead end-to-end Medical Information services for sponsor accounts, ensuring quality, compliance, contractual performance, and effective handling of enquiries and safety handoffs. Build and develop the MI team, improve processes and content systems, and represent the function in audits while partnering with internal teams and sponsor stakeholders.
Requirements
Requires 15 or more years of life sciences experience, with substantial Medical Information and/or Pharmacovigilance expertise and prior MI management or team-lead experience. Candidates should have a life sciences or pharmacy degree, preferably an advanced qualification, and experience with client relationships, global enquiries, regulatory guidance, controlled documentation, and MI databases.
Skills
- Medical Information
- Pharmacovigilance
- Team Leadership
- Team Development
- Service Delivery
- Regulatory Compliance
- Standard Operating Procedures
- Medical Enquiry Management
- Quality Control
- Audit Readiness
- Process Improvement
- Content Management
- MI Database Configuration
- Stakeholder Engagement
- Technology and Automation
Benefits
- Flexible Working Arrangements
- Career Growth Opportunities
- Performance Reviews
- Growth Planning
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Management & Leadership
- Customer Service & Support
- Science & Research
Keywords
- Medical Information
- Pharmacovigilance
- Sponsor Accounts
- Service-Level Agreements
- Medical Enquiries
- Healthcare Professionals
- Adverse Events
- Product Complaints
- Standard Operating Procedures
- Work Instructions
- Controlled Documents
- Standard Response Documents
- Frequently Asked Questions
- Global Content Libraries
- MI Databases
- Content Management Systems
- Database Configuration
- Validation
- Automation
- Artificial Intelligence
- ICH Guidelines
- Global Pharmacovigilance Frameworks
- Corrective and Preventive Actions
- Regulatory Inspections
- Sponsor Audits
- Medical Affairs
- Quality Assurance
- Regulatory Affairs
- Operational Excellence