Therapeutic Area Manager, Scientific Affairs Medical Information Scientific Engagement (SA MISE)

Johnson & Johnson•Titusville, NJ

1d•Hybrid

About The Position

Johnson & Johnson Innovative Medicine is recruiting for a Therapeutic Area Manager, Scientific Affairs Medical Information Scientific Engagement (SA MISE), to be in Titusville, NJ. 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 This is a hybrid role available in Titusville, NJ. While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply. Purpose: The Therapeutic Area Manager, Scientific Affairs Medical Information Scientific Engagement (SA MISE) is responsible for engaging healthcare professionals (HCP) and other customers in rich scientific dialogue and developing customer materials for use in response to unsolicited medical information requests. This position will serve as a point of contact for US HCP escalations. The Therapeutic Area Manager, SA MISE will evaluate voice-of-customer trends and provide insights to internal stakeholders. Additionally, this role will provide innovative solutions to optimize delivery of scientific information to customers. The Therapeutic Area Manager, SA MISE will be responsible for leading the medical information booth at scientific meetings and providing after-hours phone coverage for emergency escalations on a rotating basis. This position will conduct training sessions for scientific/product knowledge, mentor MISE team members/fellows and participate in departmental initiatives.

Requirements

BS in Pharmacy or related science field; advanced Degree (e.g. PharmD) highly preferred.
A minimum of 2-4 years in the healthcare field or pharmaceutical industry
Ability to verbally communicate scientific information to healthcare professionals
Ability to conduct literature analysis
Experience building on existing clinical foundation in pursuit of expertise in relevant therapeutic areas
Experience managing complexity and ability to work independently
Ability to collaborate with cross-functional partners/teams
Qualified to coach and mentor employees on a one-on-one basis as well as in a group
Strong computer skills (Microsoft office)
Strong organizational skills

Nice To Haves

Medical writing experience
Drug Information or Clinical Residency/Fellowship
Knowledge in developing responses to scientific inquiries from healthcare professionals and/or consumers.
Experience in gathering voice of customer/customer insights

Responsibilities

Leads the development and maintenance of scientific content for patients for assigned therapeutic area products including patient content for established products
Conducts authoring and peer review of patient scientific responses for products within assigned therapeutic area
Collaborates with the Medical Information Content Strategy and Innovation Digital team to help shape and review the innovative content formats for patient responses
Ensures high quality, personalized, cross-portfolio scientific engagement with all customers to demonstrate product and disease area expertise. Provides timely, accurate, thorough, and balanced scientific responses to unsolicited requests for information from internal and external customers consistent with regulatory guidelines and documentation standards with the Customer Relationship Management database. Conducts literature analysis as needed.
Identifies, captures, and processes adverse events and product quality complaints following regulatory and company policies
Ensures the highest standard of quality and compliance by supporting MISE quality assurance (QA) measures and confirms robust medical information provided is accurate and consistent
Leads response creation for US escalated one-off inquiries within assigned therapeutic area
Conducts peer review of US one-off response(s) created
Supports product and disease state-related scientific training
Manages scientific training content development as needed
Analyzes Voice of Customer data and identifies actionable insights to share with MISE leaders and internal partners to champion unmet data gap needs to accurately represent the voice of our most important stakeholder, our customers
Leads Medical Information Booth support at medical congresses, ensures participation in booth training, and completes of all Medical Information booth support activities at the end of the congress
Leads/participates in departmental strategic projects and other ad-hoc activities as assigned by leadership to ensure process improvement
Provides after-hours medical information support for emergency phone calls related to Johnson and Johnson products

Benefits

employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Washington –56 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
Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member
Caregiver Leave – 10 days
Volunteer Leave – 4 days
Military Spouse Time-Off – 80 hours