Pharmacovigilance Specialist

Pharmacovigilance Specialist (6-Month Contract)Toronto, ONIntroductionWe are hiring a Pharmacovigilance Specialist for our client, Eli Lilly, based in Toronto, Ontario. This is a 6-month contract that will cover a medical leave. The Pharmacovigilance Specialist will conduct thorough reviews of medical forms, ensuring accuracy and compliance with...

Pharmacovigilance Specialist (6-Month Contract)Toronto, ONIntroductionWe are hiring a Pharmacovigilance Specialist for our client, Eli Lilly, based in Toronto, Ontario. This is a 6-month contract that will cover a medical leave. The Pharmacovigilance Specialist will conduct thorough reviews of medical forms, ensuring accuracy and compliance with...

Pharmacovigilance Specialist (6-Month Contract) Toronto, ON Introduction We are hiring a Pharmacovigilance Specialist for our client, Eli Lilly, based in Toronto, Ontario. This is a 6-month contract that will cover a medical leave. The Pharmacovigilance Specialist will conduct thorough reviews of medical forms, ensuring accuracy and compliance with...

Pharmacovigilance Specialist (6-Month Contract)Toronto, ONIntroductionWe are hiring a Pharmacovigilance Specialist for our client, Eli Lilly, based in Toronto, Ontario. This is a 6-month contract that will cover a medical leave. The Pharmacovigilance Specialist will conduct thorough reviews of medical forms, ensuring accuracy and compliance with...

Pharmacovigilance Specialist Job Opportunity in TorontoWe are seeking a skilled Pharmacovigilance Specialist for our client, Eli Lilly, based in Toronto. This is a 6-month contract that will cover a medical leave.About the Role:The successful candidate will conduct thorough reviews of medical forms, ensuring accuracy and compliance with pharmacovigilance...

We are looking for a skilled Pharmacovigilance Specialist to join our team at Eli Lilly in Toronto, Ontario. As a Pharmacovigilance Specialist, you will conduct thorough reviews of medical forms to ensure accuracy and compliance with pharmacovigilance standards.Job ResponsibilitiesConduct reviews of medical forms to ensure accuracy and compliance with...

Pharmacovigilance Specialist OpportunityWe are hiring a Pharmacovigilance Specialist to work with our client, Eli Lilly, based in Toronto. This is a 6-month contract that will cover a medical leave.About the RoleConduct thorough reviews of medical forms, ensuring accuracy and compliance with pharmacovigilance standards.Collaborate closely with...

Pharmacovigilance SpecialistSalary: $65,000 - $90,000 per year (based on Toronto, ON location and industry standards)Job DescriptionWe are seeking a skilled Pharmacovigilance Specialist to join our team in Toronto, Ontario. This is a 6-month contract that will cover a medical leave.The successful candidate will conduct thorough reviews of medical forms,...

The RoleWe're seeking an experienced Content Specialist to join our team at Veeva Systems. As a key contributor, you will play a crucial role in developing high-quality documentation for our pharmacovigilance products.Veeva Vault Safety is a leading cloud-based platform designed to streamline safety reporting and compliance processes. Our mission is to...

About the RoleWe are seeking a skilled Pharmacovigilance Specialist to join our client, Eli Lilly, in Toronto, Ontario. This is a 6-month contract opportunity that will provide temporary support during a medical leave.Key ResponsibilitiesCollaborate closely with cross-functional teams, including regulatory, quality assurance, and medical affairs, to ensure...

Pharmacovigilance Specialist (6-Month Contract) Toronto, ON We are hiring a Pharmacovigilance Specialist for our client, Eli Lilly, based in Toronto, Ontario. This is a 6-month contract that will cover a medical leave. The Pharmacovigilance Specialist will conduct thorough reviews of medical forms, ensuring accuracy and compliance with pharmacovigilance...

About the RoleVeeva Vault Safety is seeking an experienced Documentation Specialist to join their team. As a Documentation Specialist, you will be responsible for creating high-quality documentation for pharmacovigilance content.What You'll DoDevelop and maintain documentation for new features and monthly releases, ensuring it is accurate, complete, and...

**This is a remote position** 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...

Job DescriptionA 6-month contract opportunity has arisen for a Pharmacovigilance Specialist to support our client, Eli Lilly, based in Toronto, Ontario. As a key member of the cross-functional team, you will conduct thorough reviews of medical forms, ensuring accuracy and compliance with pharmacovigilance standards.ResponsibilitiesCross-Functional...

**ISOLOGIC Innovative Radiopharmaceuticals** offers you an exceptional opportunity to join our dynamic team as a Production Specialist! If you have a passion for nuclear medicine and want to make a significant contribution to patient care while working in a stimulating and dynamic environment, then this opportunity is for you. **ISOLOGIC **is a national...

About the RoleWe are seeking a highly experienced Senior Clinical Safety Specialist to join our team at Brunel. As a global pharmaceutical company, we are dedicated to delivering innovative technology and products in nutrition, diagnostics, medical devices, and branded generic pharmaceuticals.This role will involve leading the clinical safety strategy for...

Zenith PV Solutions Inc. is a leading provider of a full range pharmacovigilance services to the pharmaceutical industry in Canada. Our philosophy to provide the best quality of service and focus on client satisfaction has allowed us to grow rapidly through client referrals. As we grow our team to support our growing client base, we are looking for an...

The RoleAre you a skilled Technical Writer looking for a new challenge? Do you enjoy crafting high-quality content and working in a collaborative environment?Veeva Vault Safety seeks an experienced Technical Writer who takes pride in their work and is passionate about creating engaging content for users.Key ResponsibilitiesDevelop and maintain documentation...

Play an integral role in management of daily operational activities of the Global Submissions Team within Case processing. - Responsible for managing timely submission of Global ICSRs to various Health Authorities, License Partners and CROs. - Prepare local paper submissions to US FDA in accordance with Otsuka processes. - Responsible to address daily...

Veeva Vault Safety is a leading provider of cloud-based software solutions for the life sciences industry. We are seeking an experienced Content Writer to join our team.Salary Range: $60,000 - $110,000 CADJob DescriptionThe successful candidate will be responsible for creating high-quality content that meets the needs of our users. This includes writing and...