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Added 1 min ago
JH
Research Scientist – Applied Mathematics & Reasoning for Decision Advantage
Johns Hopkins Applied Physics Laboratory
Laurel, MD
- $105,000 USD / year
…artificial intelligence, signal and image processing, sensor and data fusion, and operations research to improve how people and systems make decisions. We value mathematical rigor, strong…
Added 1 min ago
JH
Simulation & Physics Software Engineer for ISRT Scientific Applications
Johns Hopkins Applied Physics Laboratory
Laurel, MD
- $100,000 USD / year
You will integrate custom physics models, simulation components, rendering systems, data sources, and hardware interfaces into reliable, deterministic interactive capabilities.
Added 1 min ago
JH
2027 Internship - Material Sciences
Johns Hopkins Applied Physics Laboratory
Laurel, MD
- $22.6 to $47.95 USD / hour
Work alongside experienced researchers to design experiments, analyze data, and investigate relationships between materials processing, microstructure, and properties.
Added 3 mins ago
Associate and Mid-Level Software Engineers
The Boeing Company
Berkeley, MO
+ Data-Driven Feedback & Reporting: Orchestrate processes to collect, analyze, and deliver comprehensive feedback on product stability, performance, and integration issues to segment…
Added 6 mins ago
Patient Experience & Service Recovery Advisor
SSM Health
Saint Louis, MO
+ Candidates must reside within the metro St · Day Shift (United States of America)
Added 8 mins ago
Senior Full-Stack Software Engineer - Procurement Systems
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Seattle, WA
…integrations, compliance and export control, and the shared data model connecting them all. This is a high-impact, high-visibility initiative. Your work will directly eliminate manual…
Added 9 mins ago
VP Business Development
Jobgether
Remote, United States
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- $85,000 to $95,000 USD / year
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Senior Software Development Engineer, Backend
Jobgether
Remote, United States
- $156,200 to $262,600 USD / year
…development skills with a product mindset and a passion for improving developer…
Added 9 mins ago
Senior Manager of Operations & Supply Chain
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Remote, United States
Added 9 mins ago
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Scheduling Assistant, Customer Success
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- $20 to $27 USD / hour
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Reverse Engineer - Android
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Using advanced reverse engineering techniques and industry-standard analysis tools, you will help identify malicious code, data leakage, and risks affecting mobile devices and their users.
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Program Manager-Practice Optimization
Jobgether
Remote, United States
- $42.92 to $59.38 USD / hour
Full-time schedule of 40 hours per week, with an 8-hour day shift and no weekend rotation
Added 9 mins ago
Procurement Lead
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Remote, United States
…Legal, and external partners, you will turn complex spending data into actionable insights and measurable savings. You will drive transparency, improve unit economics, and ensure…
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Partner Services Manager
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Remote, United States
- $85,000 USD / year
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Network Growth Executive, Enterprise
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Manager, Communications Business Partner
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- $89,000 to $127,200 USD / year
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Interoperability Engineer I / II / SR (Workday/UKG)
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…enterprise integration solutions that enable secure and reliable data exchange across complex technology environments. This role focuses on Workday-centered integrations, connecting HR,…
Added 9 mins ago
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Head of Development
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Remote, United States
- $140,000 to $185,000 USD / year
…identify opportunities for improvement, adapt strategies based on data, and communicate progress to leadership and the Board of…
Added 9 mins ago
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Global Director, Compensation
Jobgether
Remote, United States
- $156,200 to $262,600 USD / year
…development skills with a product mindset and a passion for improving developer…
Added 9 mins ago
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Director, PBM Compliance and Regulatory Affairs
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Remote, United States
- $185,000 to $220,000 USD / year

Closed listing

Director, Clinical Development

Nashville, TN, United States

For U.S. locations that require disclosure of compensation, the starting pay for this role is between $165,000 and$215,000.

This opening has closed.

The original listing is kept below for reference.

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Job details

Pay: For U.S. locations that require disclosure of compensation, the starting pay for this role is between $165,000 and$215,000.
Experience: 7+ years of industry experience in medical device clinical development, with a strong focus on ophthalmic surgery.
Posting language: English
Posted: Aug 19, 2026

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Original job description

Archived listing. The details below describe a past opening.

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the worldfrom the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.

Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

Objectives:

The Director, Surgical Clinical Development will serve as a strategic and scientific leader for global clinical development activities supporting Bausch + Lombs surgical device portfolio. This role will focus on the design and execution of clinical strategies for innovative ophthalmic devices, including intraocular lenses (IOLs), inserters, excimer and femtosecond lasers, and phacoemulsification systems. The role will be accountable for the development and delivery of clinical evidence to support global regulatory submissions.

This leader will drive clinical strategy from early feasibility through pivotal and post-market studies, helping to shape global product launch readiness while identifying innovative, efficient pathways to expand access and accelerate approvals. This role reports to the Vice President of Clinical Evidence Generation and will play a key role in cross-functional project leadership and external engagement with regulators, investigators, and partners. Excellent communication skills are necessary to influence both internal and external stakeholders.

Responsibilities:

Lead global clinical development strategy for surgical device programs from early-stage concept through post-market activities.
Serve as the clinical voice on global regulatory submissions, ensuring strategic alignment with FDA, EU MDR/CE Mark, China (NMPA), and Japan (PMDA) regulatory pathways.
Design and oversee clinical trials including feasibility, pivotal, and post-approval studies across diverse markets.
Set direction and ensure alignment of clinical research priorities with company objectives, ensuring timely delivery of impactful clinical evidence.
Develop and author key regulatory and clinical documents including clinical investigation plans, study protocols, clinical reports, and submission dossiers.
Partner cross-functionally with R&D, Regulatory, Quality, and Commercial to translate clinical insights into product development and go-to-market strategies.
Cultivate and sustain high-impact relationships with Key Opinion Leaders (KOLs), investigators, and key external stakeholders to represent Bausch + Lombs leadership in surgical ophthalmology.
Collaborate with global regulatory and quality teams to align clinical strategy with evolving regulatory pathways and support successful global submissions.
Lead or contribute to project strategy teams and clinical sub teams, ensuring clear communication and alignment across functions.
Support market-expansion efforts through novel evidence-generation strategies tailored to payer and regulatory requirements in emerging and established markets.
Oversee clinical due diligence and provide input into product acquisitions and licensing opportunities.
Support vendor oversight, clinical operations planning, and study execution.
Contribute to the development of best practices, infrastructure, and SOPs to support a globally harmonized, agile, and compliant clinical development organization.
Manage budgets and resources.
Ensure timely submission of clinical trial data to regulatory authorities.
Identify and mitigate risks associated with clinical research activities.

Requirements:

Advanced degree (MD, OD, PhD, or equivalent) in a clinical or biomedical science discipline.
7+ years of industry experience in medical device clinical development, with a strong focus on ophthalmic surgery.
Proven track record of leading global clinical strategy and successful regulatory submissions for surgical devices.
In-depth understanding of Good Clinical Practice (GCP), ISO 14155, and global regulatory frameworks specific to medical devices.
Experience in designing and executing both pivotal and post-market studies, including registries and real-world evidence strategies.
Strategic thinker with demonstrated ability to innovate around market access and evidence generation; label expansion a plus.
Strong leadership, project management, and team collaboration skills across matrixed global organizations.
Effective communicator with the ability to represent clinical and scientific perspectives clearly to internal and external stakeholders.
Established relationships with investigators, KOLs, and global regulatory experts in surgical ophthalmology is highly desirable.

This position may be available in the following location(s):[[location_obj]]

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

For U.S. locations that require disclosure of compensation, the starting pay for this role is between $165,000 and$215,000. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors.

U.S. based employees may be eligible for short-term and/or long-term incentives. They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation.

Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.

To learn more please readBausch + Lomb's Job Offer Fraud Statement (https://performancemanager.successfactors.eu/doc/custom/BauschLomb/Bausch_job_posting_statement.docx) .

Our Benefit Programs:Employee Benefits: Bausch + Lomb (https://www.bausch.com/careers/benefits/)

Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

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Jobs in the United States