Director, Medical Safety Officer, Immunology

Johnson & Johnson, is recruiting for a Director, Medical Safety Officer, Immunology to be located in Titusville, NJ; Raritan, NJ; or Horsham, PA.

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The Pharmaceuticals Medical Safety Officer (MSO) has accountability for assessing the medical safety of assigned Janssen products and will strategically lead cross-functional matrix teams responsible for product safety and benefit risk oversight and represents Global Medical Safety (GMS) as the product spokesperson regarding overall benefit / risk.

The MSO will report to the GMS Therapeutic Area Safety Head (TASH), Immunology and oversee the safety and benefit / risk assessment of assigned products within the Immunology TA that are marketed and / or in clinical development. Collaborating with relevant functions, the MSO will ensure proactive and timely assessments of safety data to characterize the emerging and known safety profiles and benefit-risk assessment of assigned products within the TA. The MSO will communicate potential and known risks and changes to benefit / risk, when appropriate, to the TA Safety Head, the Head of Global Safety Strategy & Risk Management (GSSRM), the Chief Safety Officer (CSO), the Pharmaceuticals Chief Medical Officer (CMO), the Qualified Person for Pharmacovigilance (QPPV) Pharma, Senior Management, Health Authorities (HA), Prescribers and / or Patients. In compliance with legal and regulatory requirements, the MSO will also lead when appropriate, in the design and implementation of risk mitigation strategies to ensure the safe and appropriate use of Janssen products.

Principle responsibilities include but not limit to the following :

Strategically lead the Safety Management Teams (SMT) for assigned products. SMT responsibilities include safety surveillance (including signal detection) and risk management activities (including Risk Management Plan (RMP) and Risk Evaluation and Mitigation Strategy (REMS), as well as other activities related to managing the safety profile of assigned products (e.g., Program Safety Analysis Plan)

Provide medical and scientific expertise as the GMS representative on the Compound Development Team (CDT) and Clinical Teams

Anticipate safety concerns and influence other relevant functions including Clinical and Medical Affairs teams to minimize / mitigate patient impact by active participation in the design of the clinical protocols.

Be an active partner and core contributor of safety input to key regulatory or clinical documents including : - Risk management plans

Clinical Trial, EAP and IIS Protocols

Informed Consent Forms (ICF), including Risk Language

Safety Sections of Investigator’s Brochure (IB) and IB addenda

Safety sections of Clinical Study Reports (CSR)

Integrated Safety Summary (ISS) and Summary of Clinical Safety (SCS) for NDA / BLA / MAA filings

Periodic Benefit Risk Evaluation Report (PBRER) Safety Update Report (PSUR), Development Safety Update Report (DSUR)

Health authority queries

Company Core Data Sheets (CCDS), US and EU prescribing information

Signal Evaluations

Effectively communicate (verbally and in writing) important results of medical safety and benefit / risk management evaluations when necessary, to the GMS Leadership Team, CMO, and the Pharmaceuticals Medical Safety Council (MSC)

Actively participate and contribute to meetings with Health Authorities and external key opinion leaders

Provide medical safety leadership on due diligence teams to evaluate Licensing & Acquisition opportunities

Provide medical oversight to contractors and non-physician staff involved in preparing written safety evaluations for their assigned products. This will include : - Defining the safety question or issue requiring medical safety assessment

Developing the strategy for the safety review and analysis

Interpreting results and determining the medical importance of question or issue

Reviewing and approving (i.e., signatory) medical assessment reports, e.g. ad hoc safety reports

Work across the GMS TAs to align and improve common processes including providing strong leadership and a harmonized approach across clinical teams for safety data collection, assessment, and safety-related processes and issues

Assist in the creation, review and implementation of new SOPs, Work Instructions, guidelines, documents and other tools pertaining to safety assessment and risk management

Lead or actively participate in department-wide initiatives

Qualifications

Education and Experience :

Physician (MD or equivalent) with a minimum of 2 years of pharmacovigilance experience or other relevant experience (e.g. Clinical research, Medical Affairs)

Demonstrated skills in clinical medicine with at least 1 year of clinical practice experience

Immunology therapeutic area experience preferred

Drug safety early development experience required

Clinical development and post marketing experience required

Board Certification (if US) preferred

Medical specialization preferred

Demonstrated knowledge of principles of drug development, pharmacology, clinical trial methodology and design, medical monitoring of trials, assessment of drug risks and benefits, and safety assessment of drugs both on the market and in development and global safety regulations highly preferred

Ability to influence, negotiate and communicate with both internal and external stakeholders

Experience with Health Authority presentations is preferred.

Required Technical Knowledge and Skills :

Ability to effectively and strategically lead global cross-functional teams

Connect, collaborate and build consensus across relevant functions

Ability to think strategically, has a global mindset, big picture orientation, Ability to see the context of the entire situation, understand implications to the business

Ability to critically evaluate safety data from multiple sources (clinical trials, environment, literature, etc), assess clinical importance and potential strategic impact of the data and present the findings clearly in both written and oral communications.

Experience and knowledge of Good Clinical Practices and Pharmacovigilance regulatory requirements in US, the EU and globally, the conduct of clinical trials and for the appropriate contributions to regulatory filings, PV documents and risk management plans

Able to plan work to meet deadlines and effectively handle multiple priorities

Excellent verbal and written communication skills, including formal presentation skills. Written skills as evidenced by publication and journal articles also desirable

Fluent in written and spoken English

Proficiency in Word and PowerPoint is desired

The anticipated base pay range for this position is $194,000 to $334,650.

The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.

Employees may be eligible to participate in Company employee benefit programs such as health insurance, savings plan, pension plan, disability plan, long term incentives, vacation pay, sick time, holiday pay, and work, personal and family time off in accordance with the terms of the applicable plans. Additional information can be found through the link below.

Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

Salary : $194,000 - $334,650