JOB SUMMARY 

Reporting to the Program Manager, the Clinical Associate Program Manager is responsible for 
undertaking the management, planning, and implementation of specific programs/portfolio within a 
Patient Support Program. Additional responsibilities include education and training of new team
members, process development and improvement across Canada, and ensuring team performance 
by reviewing weekly and monthly KPI targets. Acts as the main contact for all escalations on the team 
and provides timely resolutions and responses to operational inquiries.

DUTIES AND RESPONSIBILITIES

• Ensure that the overall performance of the program and its respective services: 
patient coordination, medication management, etc. is operating successfully.
• Ensure all team members are educated on the program, and all performance standards 
for the team are met or exceeded.
• Ensure all regional operational occurrences associated with the program are 
communicated to the Program Manager.
• Ensure workload measures meet performance targets and recommend changes if they 
do not meet targets.
• Ensure KPI’s are within performance expectations.
• Ensure hiring and orientation processes are sufficient to support program needs.
• Facilitates recruitment, orientation, evaluation and retention of staff.
• Make recommendations for changes in operations and assist in the execution of these 
changes.
• Collaborate with all internal departments who deliver program related services.
• Conducts Quality Audits to assure accuracy of workflows and client-specific processes.
• Ensure quality of clinical records and CRM are maintained.
• Attends internal and external meetings with the client.
• Assistance with billing and forecasting.
• Ensure hiring and orientation processes are sufficient to support program needs.
• Complete and/or assistance in annual evaluations.
• Assist and co-lead weekly client meetings (agenda, meeting minutes, resolutions)
• Helps organize and lead team meetings.
• Must be able to identify and report AE’s to health Canada, Med Info and enter into
source system and third party systems.
• Responsible for ensuring staff follow Pharmacovigilance guidelines and reporting 
requirements.
• Responsible for assisting in manufacturer audits as needed.
• Helps with the upkeep of program work instructions and SOPs.
• Point of escalation for team members.