ASSOCIATE DIRECTOR, CLINICAL SCIENCES - OPHTHALMOLOGY

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.
om/.
Johnson & Johnson is recruiting for an Associate Director, Clinical Project Scientist - Ophthalmology to be located in Raritan, NJ, Spring House, PA, Cambridge, MA, or La Jolla, CA.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
The Associate Director, Clinical Project Scientist is a responsible member of a clinical team dedicated to the development and execution of clinical strategies and the clinical and operational implementation of a complex compound program.
The Associate Director, Clinical Project Scientist provides active scientific contribution to a cross-functional clinical team developing a molecular entity.
The Associate Director, Clinical Project Scientist provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and takes responsibility for coordinating completion of clinical study reports and supports preparation of relevant documents for regulatory filings.
This role involves extensive team matrix interactions with colleagues from several different disciplines.
The Associate Director, Clinical Project Scientist may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area.
ESSENTIAL FUNCTIONS.
Leads/Supports preparation of clinical development plans, trial protocols, and supports the operations group with trial set up and monitoring and authoring of clinical study reports.
Assists Physicians in evaluation of adverse events (pre and post-marketing) for relationship to treatment and supports the interpretation and reporting of results.
Assists Regulatory Affairs in determining requirements for any corrective actions or health authority reporting.
Interprets, reports, and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions.
Responsible for clinical data review, including medical data review, coding, in conjunction with other clinical team members.
OTHER RESPONSIBILITIES / DETAILED DUTIES.
Assists Regulatory Affairs in the development of drug regulatory strategies.
Participate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc.
Reviews medical literature and related new technologies May be asked to lead the execution of contracts.
May be asked to assess medical publications emerging from the team and its affiliates.
May be responsible, with appropriate colleagues, for review of Company advertising and promotion.
Qualifications Education and Experience.
A minimum of a Bachelor's degree with required therapeutic area experience in ophthalmology.
An advanced degree (e.
., MS, RN, RD, PhD or PharmD) is preferred.
A minimum of at least 6 years of clinical research and development experience within the pharmaceutical industry is required.
Required Technical Knowledge and Skills.
o Experience in ophthalmology product development and cross company alliances is preferred.
o Significant experience with managing/ supervising clinical trials, clinical research programs is required.
o Medical Data Review experience strongly preferred.
o Strong interpersonal and communication skills are essential.
The anticipated base pay range for this position is $ to $ USD.
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.
areers.
nj.
om/employee-benefits At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity.
That starts by creating the world’s healthiest workforce.
Through cutting-edge programs and policies, we empower the physical, mental, emotional, and financial health of our employees and the ones they love.
As such, depending on location and subject to local legislation, candidates offered employment may be required to show proof of COVID-19 vaccination or, in certain countries, secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work.
If you are invited to interview for the position, your recruiter will advise on the vaccine requirement status in your geographic location.
Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
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.