Pharmacovigilance Medical Review jobs
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…
- 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…
- Ryvis PharmaMississauga, ON
- Company events
- Casual dress
- On-site parking
- Liaise with Health Canada and Provincial Formularies on all aspects of the drug submission, follow up for review status and project updates.
- 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…
Regulatory Affairs Associate
Easily applyNutrasourceGuelph, ON- $46,563.40–$60,000.00 a year
- Full-time
- Supports literature reviews and drafting of safety and efficacy data.
- Supports reviews of product and manufacturing changes for compliance with applicable…
- HaleonSaint George's, BOT
- Full-time
- Document audit observations, assess responses, and review CAPA evidence for adequacy and timely closure.
- Support the development, maintenance, and periodic…
- View all Haleon jobs - Saint George's jobs - Audit Manager jobs in Saint George's
- Salary Search: Audit Manager GxP (GLP, GCP, GVP) salaries
- See popular questions & answers about Haleon
- GaldermaToronto, ON
- $112,000–$135,000 a year
- Full-time
- Conduct regular team meetings, performance reviews, and provide actionable feedback.
- Ensure that customer and/or patient concerns and inquiries are handled in…
- View all Galderma jobs - Toronto jobs - Sales Manager jobs in Toronto, ON
- Salary Search: National Sales Manager - Alastin salaries in Toronto, ON
- See popular questions & answers about Galderma
- GaldermaToronto, ON
- $112,000–$135,000 a year
- Full-time
- Conduct regular team meetings, performance reviews, and provide actionable feedback.
- Ensure that customer and/or patient concerns and inquiries are handled in…
- View all Galderma jobs - Toronto jobs - Sales Manager jobs in Toronto, ON
- Salary Search: National Sales Manager - Alastin salaries in Toronto, ON
- See popular questions & answers about Galderma
- RocheMississauga, ON
- $136,936.00–$179,728.50 a year
- As a Regulatory Innovation& Sustainment Professional within Pharma Development Regulatory's (PDR) Quality& Compliance capability, you will be accountable for…
- View all Roche jobs - Mississauga jobs
- Salary Search: Regulatory Innovation & Sustainment Professional - Quality & Compliance salaries
- See popular questions & answers about Roche
- Clinique MedfutureMirabel, QC
- Clinique Medfuture est une jeune entreprise en pleine croissance.
- Nous souhaitons mettre nos clients en contrôle de leur santé afin qu'ils vivent le plus…
Medical Science Liaison, Rare Disease, Canada West
Easily applyOften replies in 3 daysMedison PharmaToronto, ON M5H 3Y9- $130,000–$150,000 a year
- Support the development and review of medical materials, as required, such as scientific/medical presentations, medical education material, commercial slide…
Line Manager, Regulatory Affairs, Canada, remote
Easily applyInderoRemote- Flexible schedule
- Prepares or reviews study-specific regulatory documents/forms.
- Develops/reviews Master Informed Consent Form (ICF), as applicable, and Country ICFs.
By creating a job alert, you agree to our Terms . You can change your consent settings at any time by unsubscribing or as detailed in our terms.
People also searched:
Career Resources:
Job Post Details
Pharmaceutical Regulatory Affairs Specialist - job post
Job details
Pay
- $68,000–$100,000 a year
Job type
- Full-time
Location
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