Pharmacovigilance Medical Review jobs
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Pharmaceutical Regulatory Affairs Specialist
Easily applyMultiple openingsCRL SynergyCalgary, AB T2S 1W3- $68,000–$100,000 a year
- Full-time
- Paid time off
- Vision care
- Dental care
- Life insurance
- Disability insurance
- On-site gym
1 hire made in past 30 days- Assisting in updating methods and procedures (SOPs) related to the Quality Management System with a focus on the customer complaint and pharmacovigilance…
View similar jobs with this employerBioSyent Pharma Inc.Mississauga, ON L5N 6M1- $95,000–$120,000 a year
- Full-time
- Weekends as needed +1
- Dental care
- Life insurance
- Disability insurance
- Communicate key medical insights, opinions, and feedback from KOLs/HCPs to the BioSyent Medical Affairs team to inform and refine medical strategies.
- サイネオス・ヘルスToronto, ON
- Employee stock purchase plan
- Paid time off
- Vision care
- Dental care
- Paid sick leave
- Company car
- Conducts Source Document Review of appropriate site source documents and medical records.
- Collaboration with Sponsor affiliates, medical science liaisons and…
View similar jobs with this employerサイネオス・ヘルスToronto, ON- This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA).
- View all サイネオス・ヘルス jobs - Toronto jobs
- Salary Search: Clinical Trial Manager salaries in Toronto, ON
- サイネオス・ヘルスToronto, ON
- Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records.
- AlimentivToronto, ON
- Full-time +1
- May be required to coach peers and/or provide input for staff performance reviews.
- As the corporate subject specialist in regulatory affairs, provide regulatory…
- Jazz PharmaceuticalsMississauga, ON
- $180,000–$270,000 a year
- Dental care
- Life insurance
- Disability insurance
- Paid vacation
- Extended health care
- RRSP
- The Director, Regulatory Affairs, Canada, is a member of the Global Regulatory Affairs and Drug Safety (GRADS) team and is responsible for providing strategic…
Senior Regulatory Affairs Associate
Easily applyNutrasourceGuelph, ON- $60,000–$90,000 a year
- Full-time
- Strong technical writing skills, and ability to review and critique regulatory documents.
- Our rapidly expanding team is seeking a Senior Regulatory Affairs…
Senior Regulatory Affairs Associate
Easily applyNutrasourceGuelph, ON- $60,000–$90,000 a year
- Full-time
- Strong technical writing skills, and ability to review and critique regulatory documents.
- Our rapidly expanding team is seeking a Senior Regulatory Affairs…
View similar jobs with this employerBayshore HealthCareMississauga, ON- $67,200–$84,000 a year
- Full-time
- NCM offers enrolment and reimbursement support to physicians and medical case management services to patients.
- Nurse Case Manager(Job Number: 26003892).
View similar jobs with this employerBayshore HealthCareMontréal, QC- Full-time
- Signaler et documenter les événements indésirables conformément aux exigences de pharmacovigilance.
- NCM offers enrolment and reimbursement support to physicians…
View similar jobs with this employerBayshore HealthCareRegina, SK- Part-time
- Maintain role related, medication and pharmacovigilance training as required.
- Develop and review nursing care plans that are individualized to each patient.
View similar jobs with this employerBayshore HealthCareVancouver, BC- $70,560–$88,200 a year
- Full-time
- The Nurse Case Manager (NCM) that is referred to as a Regional Support Nurse in this program is to be a single point of contact offering medical case management…
View similar jobs with this employerBayshore HealthCareVancouver, BC- $70,560–$88,200 a year
- Full-time
- Ensure timely and compliant reporting of Adverse Events (AEs) and Product Quality Complaints (PQCs) in accordance with Health Canada pharmacovigilance…
- Bayshore HealthCareRegina, SK
- Casual
- Maintain role related, medication and pharmacovigilance training as required.
- Develop and review nursing care plans that are individualized to each patient.
- Bayshore HealthCareTrois-Rivières, QC
- Casual
- Monday to Friday
- Signaler et documenter les événements indésirables conformément aux exigences de pharmacovigilance;
- Provide patient centered care according to the established…
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Job Post Details
Pharmaceutical Regulatory Affairs Specialist - job post
Calgary, AB T2S 1W3
$68,000–$100,000 a year - Full-time
Job details
Pay
- $68,000–$100,000 a year
Job type
- Full-time
Location
Calgary, AB T2S 1W3
Benefits
Pulled from the full job description
- Paid time off
- Vision care
- Dental care
- Life insurance
- Disability insurance
- On-site gym
- Extended health care
Full job description
Job Overview
CRL Synergy, one of Canada’s largest and fastest-growing suppliers of control label products, is seeking a detail-oriented and proactive Regulatory Affairs (RAS) Specialist.CRL Synergy is seeking a Regulatory Affairs (RAS) Specialist who can thrive in a fast-paced environment that involves working in an office team environment.
The Regulatory Affairs Specialist is the site lead for all Health Canada submissions and post-market activities covering four product categories sold across Canada:
- Drugs (DIN-assigned OTC)
- Cosmetics
- Medical Devices (Class I–II)
- Natural Health Products (NHPs/NPNs)
The RAS plans, authors, files and maintains regulatory submissions and dossiers, and ensures compliant labelling/advertising.
This role will also provide quality assurance support through maintenance of the RA SOPs, ensuring they are current and implemented, perform data collection, and subsequent analysis.
The successful candidate will provide support for new product development, ensuring Health Canada and customer requirements are being met, including labelling accuracy for new and modified product.
Responsibilities
- Oversight of Pharmacovigilance program
· Collaborate with cross-functional teams to implement corrective and preventive actions (CAPA) related to customer complaints.
· Participate in risk management activities and contribute to the development of risk assessment strategies.
- Ensuring accurate record keeping and filing as per organizational procedures.
- Handle clerical and administrative activities.
- Review and assess customer complaints for adverse reactions and reportable incidents. Perform surveillance activities for ongoing product quality and safety.
- Complete Annual Summary Reports and perform screening of scientific literature for product safety information.
- Assisting in updating methods and procedures (SOPs) related to the Quality Management System with a focus on the customer complaint and pharmacovigilance program.
Qualifications
- Bachelor’s degree in a relevant field; advanced degree preferred.
- Proven experience in regulatory affairs or a related field, with a strong understanding of compliance requirements.
- Demonstrated skills in project management, including the ability to manage multiple projects simultaneously.
- Strong leadership abilities with experience in supervising teams or mentoring staff.
- Excellent analytical skills with a focus on process improvement methodologies.
- Familiarity with sales or business development processes is a plus.
- Exceptional communication skills, both written and verbal, with the ability to effectively convey complex information to diverse audiences. Join us in making a difference through compliance excellence!
Job Type: Full-time
Pay: $68,000.00-$100,000.00 per year
Benefits:
- Company events
- Dental care
- Disability insurance
- Extended health care
- Life insurance
- On-site gym
- On-site parking
- Paid time off
- Vision care
Education:
- Bachelor's Degree (preferred)
Experience:
- Regulatory Affairs: 2 years (preferred)
Work Location: In person
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