MEDICAL DIRECTOR, CATARACT SURGICAL IMPLANTS

Johnson & Johnson Vision, a member of the Johnson & Johnson family of companies is recruiting for a Medical Director, Cataract Surgical Implants located in Irvine, CA.
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.
nj.
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The Medical Director, Cataract Surgical Implants, has strategic and tactical responsibility for medical aspects related to cataract surgery implants and phaco for JJV.
Defines strategy, direction, planning, and interpretation of clinical trials/research, for both in-market products and products in development, in collaboration with Clinical Science and Clinical Operations teams.
Responsibites include AE interpretation and reporting and patient safety monitoring in collaboration with Medical Safety Officers.
Partners closely with R&D on internal development of existing portfolio and serves as medical subject matter expert on all aspects of cataract surgery.
Functions as principal internal consultant to QA on safety matters pertaining to cataract surgery including directly addressing patient and physician concerns.
Serves as medical expert with Business Development on expanded product portfolio in performing internal review of products and/or companies being considered for licensing and acquisition.
Adheres to environmental policy, procedures, and supports department environmental objectives.
Main areas of responsibility Ensure global strategic cross-functional alignment on evidence generation strategy pertaining to cataract surgical implants and phaco Provide medical leadership and support on Quality activities pertaining to product safety Provide medical expertise on product portfolio strategy to facilitate internal growth and development of new products and technology Represent JJSV in regional/global ophthalmology conferences to foster KOL relationships, discuss ideas for post-market studies, podium presentations, and publications Assist in design of clinical studies and development plans, from early transitional development activities to mature product lifecycle management strategies Serve as the Medical Monitor for all studies under his/her supervision; review, assess and report applicable adverse events and serious adverse events Participate in design and execution of clinical trial safety, product safety, and risk management plans and safety monitoring reports to regulatory agencies Interact with and coordinate appropriate medical and scientific activities with internal stakeholders (ie.
commercial, clinical research, R&D, regulatory affairs, etc..) as they relate to ongoing clinical and medical affairs projects Assist in scientific/medical education of investigators, clinical monitors, and global project team members related to therapeutic area or disease specific information Represent JJV at external meetings including advisory boards, investigator meetings, scientific association meetings, etc… Support development of scientifically accurate marketing materials (including as SME and via copy review), medical education programs, advisors, and symposia Responsible for understanding regulatory requirements related to clinical studies and accountable for complying to these requirements Assist in the scientific review and communications of investigator initiated studies May supervise one or more direct and indirect reports within medical affairs Functional and Technical Competencies.
Demonstrated ability to build collaborative relationships cross-functionally with key internal and external partners and stakeholders Ability to influence, shape and lead without direct reporting authority Ability to develop and maintain relationships with KOL’s/experts in the field Excellent knowledge in the area of Surgical Ophthalmology and Cataract Surgery In-depth knowledge and hands-on experience of post-market clinical studies, including study design, to support in-market products Awareness of Regulatory, legal, and reimbursement environment Good knowledge of study execution, pharmacovigilance, medical monitoring Ability to make clinical decisions on patient safety Ability to work in a fast-paced, innovative environment Sound knowledge of study publication processes and publications Highly customer and marketplace focused with a big picture orientation Innovative with the ability to coordinate and drive in a complex and changing environment Ability to work effectively in a matrix environment Very strong and demonstrable communication and influencing skills that can impact at a global level Awareness of and adherence to Johnson & Johnson Credo values Qualifications Requirements MD or DO degree (or non-US equivalent such as MBBS) required including 2+ years of experience in a clinical practice setting.
At least 10 years’ ophthalmology experience required.
Completion of residency in Ophthalmology required.
Fellowship in cataract, corneal, anterior segment surgery preferred.
Industry experience a plus.
The anticipated base pay range for this position is $ to $.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.
areers.
nj.
om.
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 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 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.
areers.
nj.
om/employee-benefits