Director Clinical Operations
Top Benefits
About the role
Pharma Medica Research (PMRI) Inc. is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. If your career goals align with innovation and original thinking you will be the perfect candidate to be part of an inclusive, adaptable, and forward-thinking organization. Our reputation for delivering high quality research is outstanding. At PMRI we are committed to making a difference in healthcare and people’s lives. Come join our team!
We are currently searching for a Director, Clinical Operations to join our Toronto Team! The Director, Clinic Operation plans, organizes and oversees the activities of Pharma Medica Research Inc. (PMRI) departments including kitchen, cleaning, clinic assistants, administration, clinic supplies and building management. The Director, Clinic Operations reports to the VP, Medical Affairs and/or designate.
Duties and Responsibilities
Plan, organize and manage the operations of the following clinical areas of responsibility: kitchen, facility, clinic assistants, administration, clinic supplies, and building management. Supervise the managers and supervisors from the above departments. Consult with senior management to maintain and establish standards for the provision of clinic services. Oversee the management for all clinic studies supplies and stock maintenance. Ensure general clinic duties are performed to prepare for the clinical study (e.g., tube labeling, bunk room preparation, set up bleeding stations, etc. Ensure all direct reports are specifically trained in all assigned tasks and duties. Ensure all clinical and laboratory supplies are adequately stocked on site.
Provide necessary reports as defined by the President
Ensure Health and Safety rules and regulations are adhered to at all times. Perform any tasks required by the President deemed necessary to conduct a clinical study. Other duties as required.
Qualifications
MSc in Life Sciences or related field; CCRP Certification preferred. Minimum 5 years of management experience in clinical research (preferably in a CRO setting). At least 5 years in a leadership role. Strong knowledge of GCP, ICH, FDA, and Health Canada regulations. Proven ability in strategic planning, team leadership, and cross-departmental communication. Excellent interpersonal and communication skills.
Strong computer skills in Microsoft Office Applications
We offer
Competitive compensation plan Mentorship Opportunities A benefit plan that is fully paid for by PMRI, including healthcare, dentalcare, vision care, LTD, Life Insurance, AD&D, along with a Health Spending and Wellness Spending Accounts and a voluntary RRSP Contribution Plan Opportunities for advancement and career progression A generous Employee Milestones Awards Program Corporate Discounts Program Learning Support Programs Friendly atmosphere, culture of learning Please note all applications must be eligible to work within Canada. PMRI is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested. We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.
Not the right fit? Search for Director Clinical Operations jobs in Toronto, Ontario, Canada
About Pharma Medica Research Inc.
Pharma Medica Research is a full service early phase contract research organization. We offer an innovative approach to the design and implementation of clinical trials in support of pharmaceutical and biotechnology companies' drug development projects around the globe.
- 360 bed phase I clinical capacity
- Bioanalytical lab
- Onsite organic synthesis lab
- Biorepository services
- Clinical data management
- Medical writing
- PK / Biostatistics
- Clinical trial monitoring
In addition to FIH, BA/BE, and PK/DDI studies, we have specialized skills in respiratory, transdermal delivery systems (including SIS studies), and patient PK studies.
Our reputation is built upon principles of on-time performance, responsiveness to the industry we serve, and delivery of uncompromising quality at reasonable costs.
Our client-focused approach truly differentiates us from other contract research organizations. Pharma Medica Research has developed processes that put the needs of our clients first. These include flexible study scheduling, rapid preliminary results turnaround and prompt final report delivery. Outsourcing should not be complicated. We are there to make your project implementation as simple as possible.
Similar Jobs
Director Clinical Operations
Top Benefits
About the role
Pharma Medica Research (PMRI) Inc. is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. If your career goals align with innovation and original thinking you will be the perfect candidate to be part of an inclusive, adaptable, and forward-thinking organization. Our reputation for delivering high quality research is outstanding. At PMRI we are committed to making a difference in healthcare and people’s lives. Come join our team!
We are currently searching for a Director, Clinical Operations to join our Toronto Team! The Director, Clinic Operation plans, organizes and oversees the activities of Pharma Medica Research Inc. (PMRI) departments including kitchen, cleaning, clinic assistants, administration, clinic supplies and building management. The Director, Clinic Operations reports to the VP, Medical Affairs and/or designate.
Duties and Responsibilities
Plan, organize and manage the operations of the following clinical areas of responsibility: kitchen, facility, clinic assistants, administration, clinic supplies, and building management. Supervise the managers and supervisors from the above departments. Consult with senior management to maintain and establish standards for the provision of clinic services. Oversee the management for all clinic studies supplies and stock maintenance. Ensure general clinic duties are performed to prepare for the clinical study (e.g., tube labeling, bunk room preparation, set up bleeding stations, etc. Ensure all direct reports are specifically trained in all assigned tasks and duties. Ensure all clinical and laboratory supplies are adequately stocked on site.
Provide necessary reports as defined by the President
Ensure Health and Safety rules and regulations are adhered to at all times. Perform any tasks required by the President deemed necessary to conduct a clinical study. Other duties as required.
Qualifications
MSc in Life Sciences or related field; CCRP Certification preferred. Minimum 5 years of management experience in clinical research (preferably in a CRO setting). At least 5 years in a leadership role. Strong knowledge of GCP, ICH, FDA, and Health Canada regulations. Proven ability in strategic planning, team leadership, and cross-departmental communication. Excellent interpersonal and communication skills.
Strong computer skills in Microsoft Office Applications
We offer
Competitive compensation plan Mentorship Opportunities A benefit plan that is fully paid for by PMRI, including healthcare, dentalcare, vision care, LTD, Life Insurance, AD&D, along with a Health Spending and Wellness Spending Accounts and a voluntary RRSP Contribution Plan Opportunities for advancement and career progression A generous Employee Milestones Awards Program Corporate Discounts Program Learning Support Programs Friendly atmosphere, culture of learning Please note all applications must be eligible to work within Canada. PMRI is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested. We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.
Not the right fit? Search for Director Clinical Operations jobs in Toronto, Ontario, Canada
About Pharma Medica Research Inc.
Pharma Medica Research is a full service early phase contract research organization. We offer an innovative approach to the design and implementation of clinical trials in support of pharmaceutical and biotechnology companies' drug development projects around the globe.
- 360 bed phase I clinical capacity
- Bioanalytical lab
- Onsite organic synthesis lab
- Biorepository services
- Clinical data management
- Medical writing
- PK / Biostatistics
- Clinical trial monitoring
In addition to FIH, BA/BE, and PK/DDI studies, we have specialized skills in respiratory, transdermal delivery systems (including SIS studies), and patient PK studies.
Our reputation is built upon principles of on-time performance, responsiveness to the industry we serve, and delivery of uncompromising quality at reasonable costs.
Our client-focused approach truly differentiates us from other contract research organizations. Pharma Medica Research has developed processes that put the needs of our clients first. These include flexible study scheduling, rapid preliminary results turnaround and prompt final report delivery. Outsourcing should not be complicated. We are there to make your project implementation as simple as possible.