Job Information
J&J Family of Companies Director, Safety Surveillance Physician (Oncology) in Titusville, New Jersey
Director, Safety Surveillance Physician (Oncology) - 2406190337W
Description
Johnson & Johnson, is recruiting for a Director, Safety Surveillance Physician (Oncology) to be located in Titusville, NJ; Raritan, NJ; or Horsham, PA.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at https://www.jnj.com/ .
We are Johnson & Johnson. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it. We are guided by our Credo (https://www.jnj.com/credo/) .
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall Pharmacovigilance process; this includes single case signal detection activities for selected products.
The Director, Safety Surveillance Physician (SSP) has primary responsibility for determining the medical and scientific relevance of adverse event reports within the context of the product’s safety profile as well as other products within the same therapeutic area. These responsibilities include spontaneous reports, clinical and non-clinical studies, literature reports and other sources of safety data. Additionally, SSPs participate in matrix management activities (e.g. Safety Management Team (SMT)) and provide pharmacovigilance expertise on individual case reports. SSPs support activities such as evaluating safety issues from various sources including Designated Medical Events (DME) and Events of Interest (EVOI), preparation of aggregate safety reports such as PBRERs, ad-hoc regulatory reports, Risk Management Plans, and interpretation of surveillance and product quality data.
The Director, SSP has additional responsibility to play a significant role as a senior technical leader of internal and external business initiatives.
Active participation in SSP activities which include, but are not limited to:
Analysis and assessment of SUSARs
Analysis and assessment of Critical Cases
Detection of single case signals/ through validation
Member of Safety Management Team
Active participation in Signal Evaluation
Ensuring Follow-up of all critical case/ Events of Special Interest (RMPs identified risks)
PBRER activities
Investigator Brochure activities
Watchlist activities
Analysis of Designated Medical Events (DMEs), Events of Interest (EVOIs), and similar critical cases
Review DMEs and EVOIs and determine potential signals, including DME and EVOI assessments coming from vendors
Perform validation of potential signals and coordinate with MSO
Provide recommendations for further evaluation.
Identification and analysis of new safety signals and trends by conducting systematic reviews of aggregate data
Perform signal detection activities for selected products (SMART daily alerts).
Perform validation for signals identified in reviews.
Prepare summary analysis of safety data for the SMTs. Provide recommendations for further evaluation.
Participation in pharmacovigilance matrix-teams (i.e. Safety Management Teams) responsible for pharmacovigilance activities focused on products and therapeutic areas as assigned
Support GMS Product Teams to drive change, increase efficiency, effectiveness and quality, and foster alignment, across GMS and with key stakeholders
As co-owners of sections of the Investigators Brochure for their assigned products, the SSP will provide data and assure accurate representation of adverse reactions that are considered as expected.
Qualifications
Minimum Qualifications:
A Physician (MD or equivalent) with a minimum of 2 years of clinical medicine.
A Board certification (if US) is preferred.
Medical specialization is preferred.
A minimum of 4 years of experience in industry, academia or patient care settings is required.
Oncology and Immunology therapeutic area experience preferred
Direct experience in pharmacovigilance is strongly preferred.
Experience and knowledge of Good Clinical Practices is required.
Excellent verbal and written communication skills, including ability to effectively communicate with internal and external customers.
Fluent in written and spoken English.
Working knowledge of the use of Microsoft suite of software products, including Excel and Word.
Must be able to work independently with minimum supervision to meet tight deadlines.
The anticipated base pay range for this position is $186,000 to $322,000.
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.
For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits
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 .
Primary Location NA-US-Pennsylvania-Horsham
Other Locations NA-US-New Jersey-Raritan, NA-US-New Jersey-Titusville
Organization Janssen Research & Development, LLC (6084)
Travel Yes, 10 % of the Time
Job Function Product Safety Risk Management MD
Req ID: 2406190337W