Associate Director, Scientific Communications, Hematology Oncology Horsham, PA

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

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Job Description:

Johnson & Johnson is recruiting for an Associate Director Scientific Communications Hematology Oncology in U.S. Medical Affairs (USMA) located in Horsham PA.

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 this role you will work with the Director Scientific Communications to drive the development dissemination and amplification of strategic scientific communications (i.e. manuscripts abstracts congress presentations digital medical education and MSL materials) supporting one or more products. You will be responsible for supervising medical communications vendors and provide review and some hands-on writing support.

Key Responsibilities:

• Serve as a key scientific lead for assigned asset(s) within the Hematology Oncology TA providing editorial scientific and strategic expertise for assigned projects

• Develop and execute strategic publication plans and scientific communication plans in collaboration with cross-functional TA team members (Medical Real-World Evidence Statisticians etc.)

• Integrate scientific medical and real-world evidence including health economics into scientific communications strategy

• Provide medical writing review of draft publications MSL materials and digital medical education materials

• Responsible for efficient review (and sometimes) preparation and delivery of high-quality publications presentations and abstracts; review all project-related content for accuracy and consistency

• Facilitate discussions regarding amplification and dissemination of published data and contribute to the strategic scientific communications plan including digital medical education plan

• Lead the development and execution of innovative scientific communications including interactive PDFs infographics podcasts and novel digital media with medical communication vendor support

• Coordinate development review and approval of both reactive and proactive materials for the MSL team including talking points presentations and interactive infographics

• Manage expectations timelines and budgets of the medical communication vendors

• Lead projects and deliver documents within process/timeline constraints

• Build working relationships with internal collaborators and partners along with external investigators/authors

• Guide or train cross-functional team members including external medical communication vendors on processes SOPs and standard methodologies; coach or mentor more junior colleagues

Qualifications:

• Candidates with a Doctoral degree (PhD PharmD MD or DO) with 6-8 years experience or a Masters degree with 8-10 years of related (pharmaceutical) work experience is required.

• In-depth knowledge of medical writing and publication guidelines such as GPP 2022 ICMJE ICH GCP AMA is required

• Medical Communications Vendor management experience is required

• Excellent oral and written communication as well as presentation management and problem-solving skills are required

• Demonstrated ability to work in cross-functional environments as well as ability to partner with scientists academicians clinicians and vendors.

• Be a highly motivated organized self-starter with a proven record of achievements

• Experience in Word Microsoft Office Excel Adobe Professional and Veeva

Highly Preferred:

• A minimum of 2 years publication strategy and planning experience in a pharmaceutical CRO or vendor setting is preferred

• Knowledge of the hematology oncology therapeutic area would be an advantage

Other:

• This position will be based in Horsham PA 3 days a week and may require up to 20% travel

The expected base pay range for this position is$137000 to $235750. The Company maintains highly competitive performance-based compensation programs. Under current guidelines this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporations performance over a calendar/performance year. Bonuses are awarded at the Companys discretion on an individual basis.

Subject to the terms of their respective plans 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.

Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire Employees are eligible for the following time off benefits:

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

Additional information can be found through the link below.

For additional general information on Company benefits please go to: - & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.

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