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Pharmacovigilance Associate
4 months ago
-May 8, 2023
**Job Summary****:
Primary Functions:
- Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and product requirements.
- Detailed knowledge of the following guidance documents. Good Pharmacovigilance Practices (GVP) Guidelines (GUI-0102); Risk Classification of Good Pharmacovigilance Practices (GVP) Observations (GUI-0063);
The Marketed Health Products Directorate (MHPD) guidance documents: Reporting Adverse Reactions to Marketed Health Products - Guidance Document for Industry Preparing and Submitting Summary Reports for Marketed Drugs and Natural Health Products - Guidance Document for Industry
- Assist in performing Pharmacovigilance activities for all Mint marketed drug products and API molecule level including but not limited to, collecting, and tracking incoming Adverse Drug Reactions, medical inquiries and end point follow up information.
- Assist in prepare line listing for all the ADRs received.
- Assist in keeping records for nullifying ADRs with justifications.
- Facilitate to compile ADRs, Completed CIOMS and submit to Health Canada as per the guidance.
- Assist in performing literature searches and Canada vigilance database searches.
- Liaise with Regulatory Affairs department for tracking requirements and electronic reporting if required.
- Ensure to meet quality, productivity, and delivery standards per project requirements.
- Ensure compliance to all marketed product related processes and activities.
- Help in maintain Pharmacovigilance agreement with all the vendors as required by Health Canada.
- Set up and maintain project files, standard templates, electronic forms, databases, and workflow as per project requirement.
- Assist in writing all pharmacovigilance related SOPs and work instructions.
- Perform and maintain record keeping.
- 100% compliance towards all people practices and processes and record keeping.
**Qualifications****:
Bachelor’s Degree in Life Sciences or a foreign degree equivalent to Canadian Standards.
- Excellent knowledge of medical terminology
- In depth knowledge and understanding of applicable global, regional, local clinical research regulatory requirements.
- Excellent verbal/written communication skills
- Self-motivated, flexible, receptive to changing process demands.
- Proven ability to work independently and autonomously with policies and practices.
- Proven ability to multi-task, meet strict deadlines, manage competing priorities.
- Demonstrate sound judgment and decision-making skills.
- Ability to work effectively on multiple projects simultaneously, organize own workload.
