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Safety Medical Reviewer – Immunology job at ClinChoice Canada Inc., requiring strong analytical skills, immunological knowledge, and experience in pharmacovigilance.
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Safety Medical Reviewer Consultant– Immunology
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Job Location
Job Summary
ClinChoice Canada Inc. is seeking a highly skilled Safety Medical Reviewer with expertise in immunology to join their pharmacovigilance team. The ideal candidate will have strong analytical skills, a deep understanding of immunological conditions, and experience in drug safety or pharmacovigilance. As a Safety Medical Reviewer, you will be responsible for medical review and assessment of safety data to ensure patient safety and regulatory compliance. You will conduct detailed medical reviews of Individual Case Safety Reports (ICSRs), assess adverse event reports related to immunology products, and provide medical input for case narratives and data coding. The role requires collaboration with cross-functional teams, participation in safety review meetings, and contribution to risk management plans. ClinChoice Canada Inc. is committed to inclusive, barrier-free recruitment and selection processes and values diversity. We are proud to be an equal opportunity employer. If you have a medical degree with specialization in Immunology or related field and at least 3 years of experience in pharmacovigilance, drug safety, or medical review, we encourage you to apply for this exciting opportunity.
Job Description: Safety Medical Reviewer (Immunology)
Position Title: Safety Medical Reviewer – Immunology
Location: [Remote]
Employment Type: [Contract]
Job Summary:
We are seeking a highly skilled Safety Medical Reviewer with expertise in immunology to join our pharmacovigilance team. The incumbent will be responsible for medical review and assessment of safety data to ensure patient safety and regulatory compliance. The ideal candidate will have strong analytical skills, a deep understanding of immunological conditions, and experience in drug safety or pharmacovigilance.
Key Responsibilities:
- Medical Review and Analysis:
- Conduct detailed medical review of Individual Case Safety Reports (ICSRs) to ensure accuracy, completeness, and compliance with regulatory requirements.
- Assess adverse event reports related to immunology products and determine the causality and clinical significance.
- Provide medical input for case narratives and data coding using MedDRA and WHO-DD.
- Safety Signal Detection and Risk Assessment:
- Contribute to safety signal detection activities and risk assessments specific to immunology therapeutic areas.
- Collaborate with cross-functional teams to evaluate safety signals and support safety management strategies.
- Regulatory Reporting and Compliance:
- Ensure timely and accurate submission of safety reports to global health authorities.
- Maintain compliance with regulatory guidelines, including FDA, EMA, and ICH regulations.
- Collaboration and Communication:
- Collaborate with clinical development, regulatory affairs, and other departments to provide medical expertise on safety issues.
- Participate in safety review meetings and contribute to risk management plans.
- Continuous Improvement and Training:
- Contribute to the development of standard operating procedures (SOPs) and safety review processes.
- Provide training and mentorship to junior safety reviewers and pharmacovigilance staff.
Qualifications and Experience:
- Education:
- Medical degree (MD or equivalent) with specialization in Immunology or related field preferred.
- Advanced degree (e.g., PhD, PharmD) with significant immunology experience may be considered.
- Experience:
- Minimum [3] years of experience in pharmacovigilance, drug safety, or medical review, with a focus on immunology therapeutic areas.
- Experience in clinical practice or clinical research in immunology is an advantage.
- Skills and Competencies:
- In-depth knowledge of immunological diseases and biologic therapies.
- Strong analytical and clinical judgment skills.
- Proficiency in safety databases (e.g., Argus, ArisG) and coding dictionaries (MedDRA, WHO-DD).
- Excellent communication and presentation skills.
- Detail-oriented with the ability to manage multiple tasks and prioritize effectively.
Preferred Qualifications:
- Experience with safety signal detection and risk management in immunology.
- Familiarity with global pharmacovigilance regulations (e.g., FDA, EMA, ICH).
- Previous experience in a pharmaceutical or biotechnology company is a plus.
#LI-PB1
The following disclaimer for CA must be included (remove the equal opportunities wording from the advert template in the bottom paragraph and replace with the following):
ClinChoice Canada Inc. is proud to be an equal opportunity employer, valuing and respecting diversity. We are committed to inclusive, barrier-free recruitment and selection processes. We will accommodate the needs of qualified applicants under the Human Rights Code and the Accessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 (647)724-5709 x 301.
We thank all applicants for their interest; however, only those being considered for an interview will be contacted. In accordance with Federal Personal Information Protection and Electronic Documents Act ("PIPEDA") , personal information is collected under the authority of the Act and will only be used for candidate selection.
