MA Manager, Medical Affairs

MA Manager, Medical Affairs

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:

医学事务高级经理

Location:

Asia Pacific, China, Beijing, Beijing

Work Location:

Hybrid

What you will do

Manages the design and implementation plans of medical affairs program, including identification of critical paths, budget development and tracking of all projects. Manages and delegates work of direct reports. Establishes accountability for assignments. Manages creation of educational, promotional and reporting materials for use by internal stakeholders. Manages publication planning, preparation and review. Supports technical training needs of partners. Manages review of promotional material. Implements plans for clinical trials, including protocol, staffing and budgeting as it relates to business initiatives. Ensures that trials/registries are conducted according to all applicable guidelines, regulations, company procedures and high ethical/quality standards. Implements policies and procedures for development and provision of medical and technical information pertaining to the company's products for internal use by customer and by government. Manages budget, contract negotiation and oversight of vendor activities. Executes the company's drug surveillance/product safety program which includes following up on adverse reaction reports. Provides solutions surrounding legal liability and compliance with government. Maintains collaborative working relationship between medical affairs and internal stakeholders to deliver timely and expert support to product development.

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