Senior Global Medical Affairs Leader, Bladder Cancer

Johnson & Johnson•Raritan, NJ

2d•Onsite

About The Position

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. Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. The Senior Global Medical Affairs Leader (Sr. GMAL), bladder cancer, is responsible for leading the strategy for the clinical-commercial optimization of product development and life cycle management strategies and plans for products and/or compounds within the disease area stronghold (DAS) and/or therapeutic area (TA). S/he will partner closely with the Compound Development Team (CDT), Global Commercial Strategy & Operations (GCSO) partners, Regional Medical TA/product leaders to develop integrated global medical affairs perspectives, strategies, and plans.

Requirements

An advanced scientific/medical degree (e.g. MD, PhD, PharmD, MPH or other masters level degree) is required.
A minimum of 10 years of combined relevant experience in a medical/clinical environment and/or scientific function in the pharmaceutical industry is required.
A demonstrated track record of success within Medical Affairs, clinical environment and/or scientific function is required.
Highly innovative with the ability to drive a complex and changing environment and effectively manage and resolve issues is required
Global mindset and ability to partner cross culturally/regionally is required
A demonstrated track record leading highly matrixed, cross-functional work teams comprised of high-level managers and executives is required.
Experience developing and managing strategic relationships with medical experts/opinion leaders is required
Proven ability to act as a medical spokesperson for external audiences is required.
Experience developing and managing strategic relationships with medical experts/opinion leaders is required.
Proven track record of ethical decision making is required

Nice To Haves

A M.D. or D.O. is preferred
Experience in bladder cancer is highly preferred
At least five years in the Medical Affairs environment is highly preferred.
Having an established network with medical experts/opinion leaders in in bladder cancer is highly preferred
In-depth knowledge of study/clinical methodology, study/clinical data reviews and analysis is preferred
Excellent knowledge of study execution, benefit risk management and life-cycle management are preferred
Experience in patient advocacy and engagement is highly desirable

Responsibilities

Lead the development of the Global Medical Affairs (GMAF) strategy and plan for the assigned compound(s) based on prioritized regional needs.
Collaborate with the Compound Development Team(s) (CDT) to ensure integration with the overall global compound strategy, resulting in one global R&D and Medical Affairs compound development plan, inclusive of developing a Target Product Profile representing medical affairs global and regional value needs.
Lead W-MAST (formerly GMATs) consisting of regionally designated Therapeutic Area Medical Affairs Leaders to create one medical affairs perspective and one “unified” voice on the CDT.
Provide single Medical Affairs voice into the creation of compound development and LCM strategies, plans and trial design from phase IIa through phase IV.
Lead pre- and post-launch medical activities including product/Therapeutic Area global advisory boards, medical symposia and congress activities, coordination of regional activity in these areas.
Collaborate closely with the regional medical affairs representatives to develop integrated global medical affairs strategies and plans and maintain open, two-way communication to ensure regional medical affairs is up to date on all plans, progress and decisions.
Lead development and execution of the global publication plan as well as review and approval of publications and scientific congress displays for marketed products and specified compounds in clinical development
Lead relevant patient advocacy initiatives and strategy by driving, building and enhancing strategic alliances with key national and international stakeholders, including patient advocacy groups, physician advocacy groups, academic organizations and other relevant stakeholders in response to patient needs and in support of Janssen’s global patient advocacy objectives and related strategic goals responsibility for Janssen’s patient advocacy landscape assessment and engagement strategy.
Manage the ReCAP process (review of all medical affairs sponsored clinical trials and Investigator Initiated Sponsored studies) for applicable products.
Support development of the company risk management strategy and plan as well as author and review specific sections of the Periodic benefit-risk assessment report for compounds.
Perform Medical impact assessments as required
Lead pre-approval access strategy for compound(s)

Benefits

Consolidated retirement plan (pension)
Savings plan (401(k))
Long-term incentive program
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year