Drug Safety & Data Analytics Associate

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Product Safety

Job Sub Function:
Pharmacovigilance

Job Category:
Scientific/Technology

All Job Posting Locations:
Toronto, Ontario, Canada

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for Drug Safety & Data Analytics Associate to be in Toronto, CA.

A pre-identified candidate for consideration has been identified.

However, all applications will be considered.

Purpose: The candidate will be responsible to support AE intake initiatives to ensure compliance in safety processing, reporting and follow-up activities on Janssen products.

Responsible to provide metrics, reports and ensure uploads of source documents in format acceptable in the Global Database system.

Responsible to triage, assign and/or conduct intake processing of domestic adverse case reports related to Janssen products.

The position verifies accuracy, completeness, and validity of report information during the assessment of follow-up requirements of AE reports.

Responsible to use the Canada Vigilance Adverse Reaction Online Database (CVAROD) for MAH related reconciliation activities.

Applies clinical judgment when interacting with healthcare professionals and consumers to obtain and follow up on reports of possible adverse events.

At this level, the position is expected to participate in activities aligned with the departmental and corporate business objectives.

May participate in inspection/audit readiness activities such as the Health Canada GVP Inspection.

Assists in the review and implementation of training of intake and follow-up procedural documents.

You will be responsible for:

Data Analytics, Operations, Follow-Up and Reconciliation Responsibilities


* Conduct data analysis and modelling to identify patterns and trends in large datasets


* Manage departmental adverse event report intake, initial triage, bulk upload, assignment of cases for further processing


* Develop and implement data driven strategies to improve business operations and decision making


* Colla...