Clinical Manager

🔥 0 minutes ago

🇮🇱 Israel – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 15%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Lumenis

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏭 Manufacturing

🏥 Healthcare

💄 Beauty

💰 $15M Venture Round on 2009-07

Manufacturing • Healthcare • Beauty

Lumenis develops life-changing, minimally invasive solutions for the Aesthetic and Vision markets. Lumenis creates and commercializes innovative energy-based technologies that enable a variety of skin, body, and eye care treatments. They are known for introducing solutions for previously untreatable conditions and have designed advanced technologies that have revolutionized existing treatment methods, positioning themselves as BeautyTech pioneers. With a rich history of defying technological boundaries and a commitment to innovation, Lumenis operates on a global scale, serving over 100 countries from their headquarters in Israel and employing nearly 1,500 professionals worldwide.

📋 Description

• Develop and manage end-to-end clinical project plans, timelines, and budgets from early clinical research and pre-clinical validation through clinical trials, publications, user guidelines, and post-market evidence generation • Drive cross-functional collaboration across multiple interfaces and business units • Conduct clinical and scientific assessments of standard of care, clinical trends, mechanism of action, and emerging technologies to support product development and innovation • Define pre-clinical validation strategies and lead pre-clinical evaluation activities • Lead the strategy, planning, and execution of clinical studies while ensuring adherence to protocols, ethical requirements, Good Clinical Practice, regulatory requirements, timelines, and budgets • Build and maintain relationships with cross-functional partners in R&D, product management, marketing, regulatory affairs, quality assurance, clinical training, and regional commercial teams • Lead clinical input and support for regulatory submissions and processes, including clinical rationales, clinical validations, clinical evaluation reports, and clinical development plans • Support marketing and commercial activities through scientific and medical input, including reviewing marketing collateral and developing white papers, clinical summaries, presentations, and training materials • Participate actively in scientific meetings • Communicate project status, milestones, deliverables, risks, mitigation plans, and key decisions to stakeholders

🎯 Requirements

• Bachelor's degree in life sciences, biomedical engineering, medical sciences, biotechnology, or a related field • Advanced degree preferred • Minimum of 5 years of experience in clinical project management within the medical device or pharmaceutical industry • Hands-on or demonstrated experience with pre-clinical testing, laboratory evaluations, pre-clinical study design, product performance evaluations, or validation activities for medical devices • Proven track record of managing clinical studies, validation activities, or cross-functional development projects simultaneously • Strong knowledge of Good Clinical Practice, clinical research regulations, and applicable medical device regulatory requirements • Familiarity with medical device quality systems, design control processes, risk management, and clinical evaluation documentation • Excellent organizational and leadership skills, with the ability to work under pressure, manage competing priorities, and drive projects to completion • Strong written and verbal communication skills, with the ability to present scientific and clinical information clearly to both technical and non-technical audiences • Fluent English, written and spoken • Willingness to travel globally, approximately 15%

🏖️ Benefits

• Full-time employment • Global travel opportunities (approximately 15%)