Junior Global Risk Safety Physician

Description

Kenvue is currently recruiting for a:

Junior Global Risk Safety Physician

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:
QPPV HEAD OF SAFETY SCIENCE AND POLICY

Location:
North America, United States, New Jersey, Summit

Work Location:
Fully Onsite

What you will do

The Junior Global Risk Assessment Safety Physician (JGRASP) is a physician who provides medical assessment of the product information pertinent to safety risk assessment and characterization of the emerging and known product safety profiles for assigned Kenvue portfolio products.

The JGRASP also ensures communication of potential and known risks, when appropriate, to direct management, regional medical management, Qualified Person for Pharmacovigilance (QPPV), and personnel in all other relevant functional areas.

The JGRASP is responsible for providing medical assessment of individual and aggregate safety data, supporting safety concerns and safety signals assessment, development of ad hoc safety reports and PSURs/PBRERs.

The JGRASP may be assigned development and/or ownership of processes, as needed, and shall ensure that performed activities fulfill the relevant regulatory requirements and all applicable Kenvue processes.

Key Responsibilities:

Safety data assessment and medical insights on safety deliverables for assigned products,

including but not limited to:

• Review safety data available from external and internal sources including spontaneous adverse event reports, safety data from non-spontaneous (solicited sources), results of signal detection

• Evaluation and communication of safety-related concerns (including ESI/SSI)

• Contribution to the development of signal detection strategy

• Contribution to the development of ad hoc reports

• PSUR/PBRER review

• Advice on risk mitigation actions

• Contribution to safety plans for new products and indications

• Gathering safety data for responding to queries from Regulatory Authorities, commercial partners and internal stakeholders on safety concerns and risk management including development of appropriate documentation

Requ...