Pharmacovigilance Analyst - [12 months FIXED TERM]

Pharmacovigilance Analyst - [12 months FIXED TERM]

What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated.  We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role reports to:

LIDER SEG AREA LA

Location:

Latin America, Brazil, Sao Paulo, Sao Paulo

Work Location:

Fully Remote

What you will do

Support the Local Safety Officers on applicable operational tasks and coordinate communications with Local Pharmacovigilance Organization. Work in close partnership with members of LPV across all regions to ensure a consistent global approach for Safety.

Key Responsibilities
Manage the Group Mailbox and LPV SharePoint site
Assure PSMF Contributions:

• Oversee timely delivery of the requested Pharmacovigilance System Master File (PSMF) annexes per PV regions.
• Key contributor for the Annex A (Contact details for Local PV Contacts Nominated at National Level) & C (Company Units responsible for safety data collection of solicited and spontaneous cases). 
• Ensure appropriate Quality checks being performed in accordance with PSMF Policies
• Maintenance/generation of AE/PQC contact list for PVA contracts, LSO contact list and Art 57 lists to ensure accurate information is shared with others. 
• LPV data management and training assignment
• Manage LPV members information (new hires, termination, etc.) on global database.
• Manage assignment of trainings per role, access to SharePoint and support addition on Distribution List, in close cooperation with Regional LPV Teams.

What we are looking for

Must Have

Qualification in Medical/ Health Sciences and/or proven equivalent experience in pharmacovigilance and/or data management. 

Advanced English

Nice to Have
Excellent social, organizational, oral, and written communication & presentation skills.
Detail-oriented & compliance mindset skills.
Efficient, flexible, and dynamic team player.
Able to work effectively with different cultures and instill a culture of diversity and inclusion.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
 

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.