Global Medical Safety Physician Fellow (1 of 2) - 2406161805W
Description
Janssen Research & Development, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for a Global Medical Safety Physician Fellow. This position can be located in Horsham, PA or Titusville, NJ.
At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found.
Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, cardiovascular and metabolism, and pulmonary hypertension. Please visit http://www.janssenrnd.com for more information.
The Global Medical Safety Physician Fellowship is a one-year program designed to provide qualified physicians the opportunity to gain specialized and in-depth training in key areas of pharmacovigilance within the pharmaceutical industry. This Fellowship does not provide certifications of any kind.
Principal Responsibilities:
Participate and complete training in several areas of pharmacovigilance, which include the following: safety surveillance and signal evaluation; identification of new potential safety concerns; characterization of emerging and known product safety profiles; the design and implementation of risk minimization strategies.
Provide medical expertise in the evaluation of safety data from a variety of sources (interventional and noninterventional clinical studies, post-marketing data, literature reports, and other sources of safety data) as part of the overall pharmacovigilance surveillance process; this includes medical review of individual case safety reports (ICSRs) and evaluation of aggregate safety data.
Ensure communication of potential new safety concerns and trends to the Medical Safety Officer (MSO) and the Safety Management Team (SMT).
Support SMT activities such as the evaluation of safety issues to characterize any emerging or known product safety profiles, preparation of aggregate safety reports, such as Periodic Benefit Risk Evaluation Reports (PBRERs), ad-hoc regulatory reports, and interpretation of surveillance and product quality data.
Work in a cross functional, matrix team environment.
Contribute to, when appropriate, the design and implementation of risk mitigation strategies to ensure the safe and appropriate use of Janssen Research & Development, LLC products.
Provide (2) presentations concerning Pharmacovigilance and/or pertinent medical topics to your team.
Qualifications
A minimum of a Medical Degree (Doctor of Medicine (MD)/Doctor of Osteopathy (DO) or equivalent) is required.
A minimum of 3 years of clinical experience (residency training included) is required.
Board certification/eligibility is preferred.
Experience in the Oncology and/or Immunology Therapeutic Areas preferred.
Must have excellent verbal and written communication skills (fluent in English), including formal presentation skills.
Working knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) is required.
The ability to critically evaluate data from multiple sources (clinical trials, literature, etc.), assess clinical importance and potential impact of the data, and present the findings clearly in both written and oral communications is required.
The ability to meet deadlines and effectively handle multiple priorities is required.
The anticipated base pay range for this position in the San Francisco Bay Area, CA is $139,000 to $224,825.
The anticipated base pay range for this position in all other U.S. locations is $113,000 to $195,500.
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 corporation’s performance over a calendar/ performance year. Bonuses are awarded at the Company’s discretion on an individual basis.
Employees and/or eligible dependents may be 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 may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company’s long-term incentive program.
Employees are eligible for the following time off benefits:
Vacation - up to 120 hours per calendar year
Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year
Holiday pay, including Floating Holidays - up to 13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefits
This job posting is anticipated to close on February 2, 2024. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.
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.
Primary Location NA-US-Pennsylvania-Horsham
Other Locations NA-US-New Jersey-Titusville
Organization Janssen Research & Development, LLC (6084)
Relocation Eligible: No
Job Function Product Safety Risk Management MD
Req ID: 2406161805W