Toronto On Drug safety pharmacovigilance Jobs – 16 Openings This Week

Drug Safety and Medical Information (DSMI) Coordinator
Bayshore HealthCare —Mississauga, ON
- $39,675–$52,900 a year
- Contract
- Remote
- Microsoft Powerpoint
- Microsoft Excel
- Customer service
6d
Senior Director, Pharmacovigilance and Drug Safety
Everest Clinical Research-Can —Markham, ON
- $180,000–$200,000 a year
- Nursing
- Medicine
- Oracle
- Disability insurance
- Dental care
Quick apply
12d
Clinical Research Associate - Canada
サイネオス・ヘルス —Toronto, ON
- Presentation skills
- Bachelor's
- Travel
Senior Nurse Case Manager
Bayshore HealthCare —Mississauga, ON
- $67,200–$84,000 a year
- Full-time
- Remote
- Microsoft Powerpoint
- Bilingual
- Microsoft Word
Clinical Research Associate - Sponsor Dedicated - Bilingual
サイネオス・ヘルス —Toronto, ON
- Bilingual
- In-person
4d
Clinical Trial Manager
サイネオス・ヘルス —Toronto, ON
- Presentation skills
- Bachelor's
- Travel
Reimbursement Specialist
Bayshore HealthCare —Mississauga, ON
- $52,000–$65,000 a year
- Contract
- Remote
- Bilingual
- Microsoft Excel
- Microsoft Outlook
Case Manager
Bayshore HealthCare —Mississauga, ON
- $52,000–$65,000 a year
- Full-time
- Remote
- Bilingual
- Microsoft Excel
- Microsoft Outlook
Associate Director PSS, Canada Remote Based
Fortrea —Toronto, ON
- $140,000–$180,000 a year
- Full-time
- Remote
- Doctoral degree
- English
- Master's degree
Experienced Clinical Research Associate - Sponsor Dedicated
サイネオス・ヘルス —Toronto, ON
- Presentation skills
- Bachelor's
- Travel
- Employee stock purchase plan
- Dental care
Program Manager
Bayshore HealthCare —Mississauga, ON
- $68,775–$91,700 a year
- Full-time
- Remote
- Customer service
- Public speaking
- Project management
11d
Manager, Quality Assurance
Shoppers Drug Mart / Pharmaprix —Toronto, ON
- $80,000–$110,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
11d
Chief Architect
Sitero LLC —Markham, ON
- Full-time
- Hybrid work
- Medicine
- Azure
- Computer Science
Quick apply

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Senior Director, Pharmacovigilance and Drug Safety
Everest Clinical Research-Can —Markham, ON
Phase 1 Infrastructure (US Focus): Lead the architectural design and implementation of the CRO’s initial US post-marketing safety infrastructure, configuring…
$180,000–$200,000 a year
Quick apply
12d
Manager, Quality Assurance
Shoppers Drug Mart / Pharmaprix —Toronto, ON
Reporting directly to Senior Director, Quality Assurance and Regulatory Affairs, the incumbent will be responsible for quality and regulatory management…
$80,000–$110,000 a year
11d

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drug safety pharmacovigilance jobs near toronto on

Drug Safety and Medical Information (DSMI) Coordinator

Bayshore HealthCare -
Mississauga, ON

Apply Now

Job details

Contract
$39,675–$52,900 a year
6 days ago

Qualifications

Microsoft Powerpoint
Computer operation
Microsoft Excel
Customer service
Call center
Computer skills
Communication skills

Full job description

Drug Safety and Medical Information (DSMI) Coordinator (Job Number: 26004137)

Primary Location:ON-Mississauga

Pharma

Employee Type:Contract

Pay Rate From:$39,675

Pay Rate To:$52,900

Description:

This is a contract opportunity with an anticipated end date of August 2027.

JOB SUMMARY
The Drug Safety and Medical Information (DSMI) Coordinator is responsible for managing AE/PV inbox and supporting the collection, processing, quality check and reporting of Safety events (Adverse Events and/or Product Quality Complaints) and handling Medical Information (MI) inquiries. The incumbent will represent the Scientific Affairs Department at Bayshore Specialty Rx both internally and externally as required and ensure compliance with Canadian Adverse Event reporting guidelines, Good Pharmacovigilance practices and Medical Information practices.

DUTIES AND RESPONSIBILITIES

Manage AE/PV inbox and conduct follow ups as required.
Perform data entry of safety events into internal database (CRM).
Retrieve source emails and source documents from the internal database.
If needed, assist with collection, processing, quality check and reporting of Safety events (initial and follow-up) as per the program requirements.
If needed, correct any errors that were identified in the submitted AE reports.
If needed, conduct investigation for quality issues and collect all the information to complete CAPA.
Conduct follow-ups for information from initial reporter and fill in gaps as necessary.
If required, support with reconciliation activities as per the program requirements.
If required, support/conduct activities related to source data verification as per the program requirements and/or PV agreement.
Provide and support medical information services and participates in coverage after business hours, as required.
Use available resources and FAQs to provide accurate and timely responses (verbal and/or written) to medical information queries.
Ensure timely and compliant reporting of Adverse Events (AEs) and Product Quality Complaints (PQCs) in accordance with Health Canada pharmacovigilance requirements and guidelines, including accurate documentation, appropriate escalation, and effective collaboration with internal stakeholders and regulatory teams.
Support with audits as needed.
Build excellent rapport with the internal and external customers.
Maintains confidentiality of patient, client, and corporate information at all times.
Participates in proactive Health and Safety activities while performing all duties.
Is responsible to notify immediate Supervisor of any Health and Safety risks or concerns.
Employee will maintain relevant level of knowledge of ICH (International Conference on Harmonization), GDP (Good Documentation Practices), GCP (Good Clinical Practice), Health Canada GVP (Good Pharmacovigilance Practices), Health Canada Adverse Event Reporting guidelines, and familiarity with Canada Vigilance-MedEffect Program, as appropriate to their hired role which is to be provided at time of hire and on an as needed basis. With this knowledge the employee will perform the work as required by their assigned function and will be provided with regular updates as required.
Participates in processes relating to regulatory and/or contractual reporting requirements.
Adheres to Bayshore’s Policies and Procedures.
Completes other tasks as requested/required.

Qualifications:

QUALIFICATIONS
EDUCATION

Degree or Diploma in a health and life sciences related field or equivalent combination of education and healthcare experience.

EXPERIENCE

1-2 years of PV experience or related Healthcare work experience (in Drug/Medical Information, Medical Affairs, Regulatory Affairs, Clinical Trials or Healthcare call center environment).
Knowledge of Health Canada guidelines on Reporting Adverse Reactions for Marketed Health Products, Global PV regulations, ICH guidelines and Pharmacovigilance auditing.

OTHER SKILLS AND ABILITIES

Excellent written, verbal communication and facilitation skills.
Excellent organizational & critical thinking skills.
Strong and proven attention to detail.
Ability to work with strict timelines and handle multiple priorities.
Flexible, adaptable, and able to work under pressure and convey a sense of urgency.
Demonstrated initiative and accountability and be able to work under minimal supervision.
Excellent customer service skills to deal with client questions, sometimes under difficult circumstances. Be able to handle challenging discussions.
Team Player with ability to function in a multi-disciplinary environment and promote collaboration.
Proficiency with basic computer skills, excel, PowerPoint, reporting tools etc. Prior experience with a Pharmacovigilance reporting software and/or safety databases applications an asset.

Apply Now

Refine Your Search

drug safety pharmacovigilance jobs in toronto on

Drug Safety and Medical Information (DSMI) Coordinator

Senior Director, Pharmacovigilance and Drug Safety

Clinical Research Associate - Canada

Senior Nurse Case Manager

Clinical Research Associate - Sponsor Dedicated - Bilingual

Clinical Trial Manager

Reimbursement Specialist

Case Manager

Associate Director PSS, Canada Remote Based

Experienced Clinical Research Associate - Sponsor Dedicated

Program Manager

Manager, Quality Assurance

Chief Architect

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