Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click’s treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click’s platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases.

Click Therapeutics

Cybersecurity Project Analyst

Executive Assistant & Office Manager

Marketing and Communications Associate

Senior Product Manager

Senior Business Development Manager/Associate Business Development Director

Business Development Director

Senior Program Manager

Click Therapeutics, Inc. develops, validates, and commercializes software as prescription medical treatments (Digital Therapeutics™) for unmet medical needs, delivering FDA-regulated treatments to smartphones. They apply technical and scientific rigor to create engaging experiences with compelling clinical outcomes, expanding their platform with AI/ML tools for diverse therapeutic areas like psychiatry, neurology, and oncology. Consistently named a best place to work, Click fosters a diverse workforce. They seek a Cybersecurity Project Analyst to join their information security program, collaborating with the Cyber Team and engineers to design, test, implement, and monitor security measures. This hybrid role is based in Tribeca, NYC, requiring at least 3 days in office weekly.

<h1 class="text-3xl md:text-4xl font-extrabold mt-6 mb-4 text-gray-900 tracking-tight">Who We Are:</h1>Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click’s treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click’s platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn.<h1 class="text-3xl md:text-4xl font-extrabold mt-6 mb-4 text-gray-900 tracking-tight">About the Role:</h1>We're looking for a Cybersecurity Project Analyst to join our team at Click Therapeutics, Inc. In this role, you'll be a key player in our information security program, working alongside the Cyber Team, engineers, and senior security experts. Your main responsibilities will include helping to design, test, implement, and monitor the security measures that protect our company.This position is based out of Click’s headquarters located in Tribeca, NYC, at the center of one of the fastest-growing digital health communities. We have a hybrid working model that consists of at least 3 days in office each week.<h1 class="text-3xl md:text-4xl font-extrabold mt-6 mb-4 text-gray-900 tracking-tight">Responsibilities:</h1><ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">Maintain awareness of emerging cybersecurity threats, regulatory requirements, and industry best practices across Information Security, Application Development, GRC to help drive organizational change.</li><li class="leading-relaxed">Identify and assess vulnerabilities in critical assets, customer network, and systems; coordinate and manage remediation activities to closure.</li><li class="leading-relaxed">Maintain and mature the Third-Party Risk Management lifecycle, including onboarding, due diligence, re-assessments, and risk mitigation.</li><li class="leading-relaxed">Monitor and track risk, risk exceptions and compensating controls; ensure risk acceptance processes are documented and approved in accordance with governance policies.</li><li class="leading-relaxed">Develop, implement, and maintain risk and compliance programs aligned with NIST, ISO 27001, SOC 2, and CyberEssentials frameworks.</li><li class="leading-relaxed">Create, update, and maintain standard operating procedures (SOPs) and information security policies (ISPs) to ensure alignment with organizational posture and compliance requirements.</li><li class="leading-relaxed">Lead internal and external audits and support compliance efforts, including SOC 2, ISO-27001, and other regulatory frameworks.</li><li class="leading-relaxed">Assist with incident response activities, including triaging alerts, and investigating security events to system and network security alerts.</li><li class="leading-relaxed">Lead monthly phishing simulation campaigns and analyze results to strengthen the organization’s security awareness.</li><li class="leading-relaxed">Manage and enhance the Security Awareness Training program, ensuring engagement and ongoing relevance to emerging threats and best practices.</li><li class="leading-relaxed">Participate in the change management process, ensuring that security requirements and impact assessments are properly addressed.</li><li class="leading-relaxed">Collaborate with the Cloud and Application engineering teams to provide security-focused guidance during the design and implementation phases.</li><li class="leading-relaxed">Work as part of a cross-functional team of engineers and analysts, contributing in a respectful, inclusive, and collaborative environment.</li><li class="leading-relaxed">Manage projects under minimal supervision and create progress reports.</li></ul><h1 class="text-3xl md:text-4xl font-extrabold mt-6 mb-4 text-gray-900 tracking-tight">Qualifications:</h1><ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">1+ years of hands-on experience in cybersecurity, information security, or a related field.</li><li class="leading-relaxed">Strong eagerness to learn, take initiative, and engage with new and evolving tasks.</li><li class="leading-relaxed">Effective verbal, written, and interpersonal communication skills.</li><li class="leading-relaxed">Foundational knowledge and understanding of IT risk assessments of potential and current information security risk.</li><li class="leading-relaxed">BS degree in Computer Science, Cyber Security or related field or equivalent work experience.</li></ul><h1 class="text-3xl md:text-4xl font-extrabold mt-6 mb-4 text-gray-900 tracking-tight">Preferred Qualifications:</h1><ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">Experience working with cloud-based environments and microservices architecture, including configuration, operation, and maintenance (e.g., AWS).</li><li class="leading-relaxed">Familiarity with compliance and risk management requirements in regulated industries such as healthcare, or related industries.</li><li class="leading-relaxed">Working knowledge of common security frameworks (e.g., NIST, SOC 2, ISO27001)</li><li class="leading-relaxed">Familiarity with developing within an agile scrum planning methodology</li><li class="leading-relaxed">Relevant certifications such as CC, SEC+, CISA, CISM.</li></ul><h1 class="text-3xl md:text-4xl font-extrabold mt-6 mb-4 text-gray-900 tracking-tight">Compensation:</h1>The base salary range for this position is between: $85,000 - $110,000. The final base salary will be dependent upon skills, experience and location. In addition to the base salary, Click Therapeutics offers an annual performance-based cash bonus and a generous equity package.<h1 class="text-3xl md:text-4xl font-extrabold mt-6 mb-4 text-gray-900 tracking-tight">Benefits:</h1>The role includes great benefits and is an excellent wealth-building opportunity at a fast-growing pre-IPO company in a nascent and extremely exciting space.Competitive Salary with Annual Review | Cash Bonus | Stock Options | 5% 401(k) matching | Medical | Dental | Vision | Life Insurance | Voluntary Benefits | Unlimited PTO | Uber One | Nectar Rewards | One Medical | Fertility Support | Fitness Reimbursement | Bike Membership | Professional Development Stipend | DoorDash and Catered Lunches | Parent Benefits | LinkedIn Learning | Gemini Enterprise Stack | Industrious Workspaces | Commuter Subsidies | Flexible Work Arrangement | Choice of Mac or Windows | Sponsored Company Events | Office Snacks and Beverages | Much More…<h1 class="text-3xl md:text-4xl font-extrabold mt-6 mb-4 text-gray-900 tracking-tight">Equal Employment Opportunity:</h1>Click Therapeutics is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Click Therapeutics also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Click Therapeutics in the U.S. In certain circumstances it may be advantageous to Click Therapeutics to support the application(s) for temporary visa classification and/or sponsor applications for permanent residence so that a foreign national colleague can accept or remain in a work assignment in the U. S. For certain classes of temporary visas, the resulting work authorization may be specific to Click Therapeutics and the specific job and/or work site. Click Therapeutics may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residency and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons. Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Click Therapeutics in the U.S. and, if so, whether that authorization permits them to work in the job they seek. In no case should Click Therapeutics support of a colleague's temporary visa application or sponsorship of a colleague for permanent residence be construed to guarantee success of that application or amend or otherwise invalidate the "at-will" employment relationship between the colleague and Click Therapeutics.<h1 class="text-3xl md:text-4xl font-extrabold mt-6 mb-4 text-gray-900 tracking-tight">Recruitment Phishing Scams:</h1>Fake job advertisements and offers are increasingly appearing on the internet. If you have encountered a job posting or have been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond and report it to the Federal Trade Commission and the FBI at https://www.ic3.gov/Home/ComplaintChoice.Please be mindful of the following:<ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">Click Therapeutics will only reach out to you through an “@clicktherapeutics.com” email address.</li><li class="leading-relaxed">Other than your email address or telephone number, which you may provide via a job application portal, Click Therapeutics will never ask you to provide personally identifiable information about yourself (such as a Social Security Number or Driver’s License Number) via a messaging application (like that used on the LinkedIn platform or Microsoft Teams).</li><li class="leading-relaxed">Click Therapeutics will conduct interviews face-to-face over Zoom.</li><li class="leading-relaxed">All job postings will be listed on the Click Therapeutics official career page.</li></ul>

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Philips

Post Market Surveillance (PMS) Specialist

Embedded Software Security development engineer

Senior Channel Sales, Emergency Care

Security Architect

Central Marketing Intern

Senior Supplier Quality Engineer

Account Executive- Imaging System- Japiur

AI Solution Architect (CG70)

Project Coordinator

The Post Market Surveillance (PMS) Specialist is a key member of the DXR Quality team, responsible for managing activities related to post-market product safety surveillance and risk management. This role involves creating and maintaining PMS Plans and Reports, conducting Periodic Quality Review Board Meetings, preparing PSURs, and facilitating Post Market Risk Assessments. The specialist acts as a liaison between various departments to ensure end-to-end execution of PMS and Risk Management processes, reviewing aggregate data, and providing recommendations for escalation.

At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life.For more than 130 years, we have been creating technologies and innovations that improve people's lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health.Together, we deliver better care for more people because we believe that every human matters.

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<h2 class="text-2xl md:text-3xl font-bold mt-10 mb-4 border-b pb-2 text-gray-800">Job Title</h2>Post Market Surveillance (PMS) Specialist<h2 class="text-2xl md:text-3xl font-bold mt-10 mb-4 border-b pb-2 text-gray-800">Job Description</h2>Job Title : Post Market Surveillance (PMS) SpecialistThe Post Market Surveillance (PMS) Specialist is a key member of the DXR Quality team and serves as a subject matter expert to support all aspects of Post-Market Surveillance.Key Responsibilities:The PMS Specialist is responsible for managing activities related to post-market product safety surveillance and risk management including:<ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">Creation and maintenance of PMS Plans</li><li class="leading-relaxed">Creation and maintenance of PMS Reports</li><li class="leading-relaxed">Conduct Periodic Quality Review Board Meetings and creation of Periodic Quality Review Reports</li><li class="leading-relaxed">Preparation and update of PSURs</li><li class="leading-relaxed">Audit and Inspection support</li><li class="leading-relaxed">Own and effectively drive CAPAs on post-market surveillance</li><li class="leading-relaxed">Facilitate Post Market Risk Assessment including Issue impact assessments, Health hazard evaluation, etc.</li></ul>Your role:<ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">You are responsible for managing activities related to post-market product safety surveillance and risk management.</li><li class="leading-relaxed">Serves as a liaison between Medical Affairs, Clinical Affairs, Research & Development, Services, and Complaint Handling to ensure Post Market Surveillance (PMS) and Risk Management (RM) processes are executed end-to-end (E2E).</li><li class="leading-relaxed">Reviews and prepares reports on aggregate data and provides recommendation for further escalation.</li><li class="leading-relaxed">Prepare/review complaint trend analysis, product risk assessments including Health Hazard Evaluations, clinical evaluation reports, risk management reports and FMEAs.</li><li class="leading-relaxed">Assists in benchmarking best practices with world-class organizations, interfaces with notified body, and/or other regulators, and provides input to establish metrics.</li></ul>Post Market Surveillance (PMS)<ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">Ensures standard PMS processes across business unit is established</li><li class="leading-relaxed">Assures consistent PMS plans exists for all products</li><li class="leading-relaxed">Assures consistent and standard process exists to perform proactive surveillance (e.g. regulatory database searches, literature reviews) and reactive surveillance (e.g. complaints handling, field actions).</li><li class="leading-relaxed">Assures consistent PMS Reports/PSURs for all products.</li><li class="leading-relaxed">Conduct periodic quality board meeting to review PMS data collected according to the PMS plan and take appropriate actions as necessary to ensure the product remains safe and compliant.</li><li class="leading-relaxed">support Complaint trending investigation, signal assessment & escalation</li><li class="leading-relaxed">Assesses significant triggers & safety concerns during periodic quality review meeting and assures standard approach for signal disposition; incorporate findings in PMS reports and trigger risk management file update, as required.</li></ul>Patient Safety and Regulatory Reporting<ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">In collaboration with Data trending and analytics and Medical Affairs, monitors and assesses safety signals, and recommends actions.</li><li class="leading-relaxed">Support in assessment of product relationship to reported complaint</li><li class="leading-relaxed">Assures standard regulatory reporting assessment criteria for PMS activities</li><li class="leading-relaxed">Provides input to clinical conclusion to be included in the reports to competent authorities.</li><li class="leading-relaxed">Enable correction & removal decision making by facilitating on time and accurate post market risk assessments.</li></ul>Risk Management<ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">Support standard Risk Management processes</li><li class="leading-relaxed">Facilitate post-market risk assessments including issue impact assessment, health hazard evaluations.</li><li class="leading-relaxed">Collaborate with cross-functional stakeholders including R&D, Services, Complaint handling, Medical Affairs, Clinical Affairs, Engineering, etc. to drive meaningful post market risk assessment of issues.</li><li class="leading-relaxed">Support the preparation and/or review of Risk management documents including risk management plans, risk matrix status reports, PPMRR, etc.</li></ul>PMS and RM input into Product Development<ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">Represent PMS interests in multi-disciplinary teams during product development.</li><li class="leading-relaxed">Assures development and completion of PMS deliverables throughout the design process.</li><li class="leading-relaxed">Provides input of PMS related product risk & quality issues during the development of new products.</li></ul>You're the right fit if:<ul class="list-disc list-inside my-5 pl-5 space-y-2 text-gray-700"><li class="leading-relaxed">You have a minimum of Bachelor's degree in Life Sciences, Biomedical Engineering, or a related technical field.</li><li class="leading-relaxed">You have 4-8 years' experience in Post Market Surveillance within FDA/EU-MDR regulated Medical Device environments with a focus on post-market surveillance plans/reports and post market risk assessment - Mandatory</li><li class="leading-relaxed">You have detailed knowledge of medical device regulations, requirements, and standards, such as 21 CFR Parts 803, 806, and 820, ISO 13485, ISO 14971, European Medical Device Directive (93/42/EEC), EU Medical Device Regulation (EU MDR), Canadian Medical Devices Regulation (SOR/98-282), etc - Mandatory</li><li class="leading-relaxed">You have excellent communication (written and oral) and stakeholder management skills, with the ability to influence at all levels.</li><li class="leading-relaxed">You have a passion for simplification and optimizing processes and workflows, identifying opportunities for automation and software tools that improve productivity, quality and compliance.</li><li class="leading-relaxed">Product Knowledge on Diagnostic X-rays is preferred.</li></ul>In return, we offer youAt Philips, we are driven by our mission to improve the lives of 3 billion people per year by 2030, and every day we move closer to achieving our goal by creating cutting-edge solutions that lead to confident diagnosis, improved care, and increased quality of life for patients. Thanks to our employees who share our passion for improving lives, we are at the forefront of the Healthcare industry leading in image guided interventions, ultrasound, patient monitoring, cardiology informatics, sleep therapy, respiratory care and services.How we work at PhilipsOur newly-adopted hybrid work concept fuses flexibility with collaboration to deliver great outcomes for our people and our customers. We are embracing an approach wherein we spend more time together than apart – which for full-time employees translates to an average of at least 3 days working from the office and up to 2 days from home – for our hybrid roles. Hybrid work flexibility means people can meet the changing demands of work and home in the most balanced, productive, and healthy way.Our hybrid working model is defined in 3 ways:We believe in the importance of impactful collaboration: There's a certain energy when everyone’s in the same room that can heighten idea generation and creative friction needed for problem-solving.We embrace flexibility: Choosing where, when and how to work can vary according to task and team schedules. Flexibility isn’t office or online, it means choosing the space that works best for you, your teams and our customers on a case-by-case basis.We want to be at our best: The way we work and our workspaces are designed to support our well-being, offer career advancement opportunities, and enable us to be at our best.Why should you join Philips?Working at Philips is more than a job. It’s a calling to create a healthier society through meaningful work, focused on innovative, customer-first health technology solutions. Help us improve the health and well-being of billions of people, every year. Ultimately creating a career that no one could have planned for. Even you.

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This assessment gives us an idea of your C++ skills- Companies that evaluate this skillset in interviews: Rockstar Games, Ubisoft, Mayhem Studios, etc.- 10 Multiple Choice questions- Average time to complete: 7 to 10 minutes

Let's assess your Data Structures! - This assessment gives us an idea of your problem solving skills using DSA- Companies that evaluate this skillset in interviews: MPL, LILA Games, GSN Games, etc.- 10 Multiple Choice questions

Data Structures and Algorithms

Let's assess your Programming Patterns! ????- This assessment gives us an idea of your code architecture skills- Companies that evaluate this skillset in interviews: Dirtcube, PTW, Playshifu, etc.

Programming Patterns

Let's assess your OOPs skills! ????- This assessment gives us an idea of your fundamental OOPS concepts and Solid principles skills- Companies that evaluate this skillset in interviews: Hitwicket, GSN Games, Tomo Club, etc.

Object Oriented Programming

Let's assess your Unity Skills ????- This assessment gives us an idea of your Unity fundamentals- Companies you can apply for after taking this assessment: Godspeed games, Salvation Games, nCore Games, etc.