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Description The Services Management Coordinator plays a crucial role in the delivery of healthcare services for patients within the assigned area. The Services Management Coordinator serve as liaison for patient care activities in specific program and ensures coordination of care around the course of the patient visit as well as subsequent patient interactions between visits. The Services Management Coordinator is responsible for multiple components of care coordination within the program(s). Specifically, Services Management Coordinators are responsible for providing administrative assistance to our providers, nurses, medical directors, medical review and case management team. This is for the program's Suffern Clinic. Responsibilities • Plays a lead role in the navigation of care and ensures that patients understand their overall program benefits as well as what they can expect the program to provide. This may include but is not limited to: liaison with Physicians, Patients education, • Sets goals with patient and care team to coordinate care, documents goal in program dashboard/calendar tool. Follow ups to be tracked include visit status reminders, scheduled follow up and specialty appointments, authorization submitted for review., • Ensures that all orders placed by the providers (internal and external) are authorized after confirming the service falls under the patients covered services., • Services as the primary point of contact to education patients pharmacy benefits, and assist with obtaining prior authorizations when applicable. This may include: Submitting refill request/confirm patients preferred pharmacies; verify coverage., • Organizes correspondence and future program plans for the patient based on program interactions in the electronic medical record as well as in the program benefits systems. This involves ensuring that a plan is made with next steps in the process., • Offers extensive patient navigation between program visits and other encounters. This includes detailed discussion with the patient to review next steps and resources, facilitation of patient concerns review, questions or concerns related to coverage.., • Educates and communicates closely with the patients to ensure they have a full understanding of the benefits offered by the program. Patient education provided on all relevant program benefits., • Provides recommendations for process improvement and services improvement aimed at improving patient experience, and participates in ongoing pilot programs to improve patient engagement., • Additional duties as assigned Qualifications • Bachelor’s degree or equivalent experience., • 3 years’ experience in healthcare/customer service or relevant experience. Compensation The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $66482.07 - $72800.15 Annually. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits. Employer Description Strength through Unity and Inclusion The Mount Sinai Health System is committed to fostering an environment where everyone can contribute to excellence. We share a common dedication to delivering outstanding patient care. When you join us, you become part of Mount Sinai’s unparalleled legacy of achievement, education, and innovation as we work together to transform healthcare. We encourage all team members to actively participate in creating a culture that ensures fair access to opportunities, promotes inclusive practices, and supports the success of every individual. At Mount Sinai, our leaders are committed to fostering a workplace where all employees feel valued, respected, and empowered to grow. We strive to create an environment where collaboration, fairness, and continuous learning drive positive change, improving the well-being of our staff, patients, and organization. Our leaders are expected to challenge outdated practices, promote a culture of respect, and work toward meaningful improvements that enhance patient care and workplace experiences. We are dedicated to building a supportive and welcoming environment where everyone has the opportunity to thrive and advance professionally. Explore this opportunity and be part of the next chapter in our history. About the Mount Sinai Health System: Mount Sinai Health System is one of the largest academic medical systems in the New York metro area, with more than 48,000 employees working across eight hospitals, more than 400 outpatient practices, more than 300 labs, a school of nursing, and a leading school of medicine and graduate education. Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time — discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. Through the integration of its hospitals, labs, and schools, Mount Sinai offers comprehensive health care solutions from birth through geriatrics, leveraging innovative approaches such as artificial intelligence and informatics while keeping patients’ medical and emotional needs at the center of all treatment. The Health System includes more than 9,000 primary and specialty care physicians; 13 joint-venture outpatient surgery centers throughout the five boroughs of New York City, Westchester, Long Island, and Florida; and more than 30 affiliated community health centers. We are consistently ranked by U.S. News & World Report's Best Hospitals, receiving high "Honor Roll" status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology. New York Eye and Ear Infirmary of Mount Sinai is ranked No. 12 in Ophthalmology. U.S. News & World Report’s “Best Children’s Hospitals” ranks Mount Sinai Kravis Children's Hospital among the country’s best in several pediatric specialties. The Icahn School of Medicine at Mount Sinai is ranked No. 11 nationwide in National Institutes of Health funding and in the 99th percentile in research dollars per investigator according to the Association of American Medical Colleges. Newsweek’s “The World’s Best Smart Hospitals” ranks The Mount Sinai Hospital as No. 1 in New York and in the top five globally, and Mount Sinai Morningside in the top 20 globally. Equal Opportunity Employer The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization.

About Us Imagine the innovation and expertise behind the world’s leading cosmetic brands, brought to you by a distinguished Italian company with a legacy of excellence. Since 1972, Intercos Group has been at the forefront of color cosmetics, pencils, nail polish, skincare, and personal care products. We pride ourselves on being the only cosmetics manufacturer that combines top-tier quality and advanced technology with a global reach and a personalized touch. With 16 commercial offices and 16 production facilities across 12 countries, Intercos Group brings a local approach to a global stage. We continually set the standard for beauty, crafting exceptional product lines for brands worldwide. As one of the largest suppliers in the cosmetics industry, we are a leading force in the research, development, and production of beauty products, shaping the future of the industry with every season. Position Summary The Chemist is responsible for all technical activities related to new and existing formulation, innovation and 1st production scale-up of new formulations in Congers, NY. Essential Functions • Lead formulation and development of powder-focused cosmetic products while also formulating and supporting development of emulsion and anhydrous technologies as project needs arise., • Facilitate end-to-end development for assigned projects, including innovation, line extensions, reformulations, and performance upgrades across powder, emulsion, and anhydrous categories., • Identify and integrate new or improved raw materials, formulation technologies, and processing methods to elevate product performance while respecting constraints such as cost targets, regulatory requirements, and client blacklists., • Collaborate directly with clients to define formulation targets, troubleshoot issues, and deliver technical solutions aligned with brand expectations., • Provide technical support through clear verbal communication, written documentation, and formal presentations to internal teams and external customers., • Conduct proactive research to scout emerging concepts, advanced materials, new texture formats, and global innovation opportunities relevant to powders, emulsions, and anhydrous formulations., • Partner cross-functionally with Marketing, Manufacturing, Quality, Regulatory, Packaging, and Corporate Applied Research to ensure alignment, • Monitor preliminary product stability for new and existing formulations., • Manage multiple concurrent projects in a high-speed, deadline-driven environment, providing frequent updates to managers and stakeholders., • Execute all formula creation, customization, and documentation within DEVEX, ensuring compliance with SOPs, BPM communication standards, and Intercos development protocols., • Support global standardization efforts by collaborating with Corporate Applied Research to harmonize processes, testing methods, and technical databases., • Maintain organized laboratory notes, batch records, and project documentation, reviewing all activities with the direct supervisor., • Perform additional responsibilities as required. Job Qualifications • Bachelor’s Degree in a Scientific Discipline such as Chemistry, Biology, Physics, or related field., • Understanding of cosmetic formulation science, with emphasis on powder technology (e.g., pigments, binders, dispersions, powders processing)., • Working knowledge of emulsion and anhydrous formulation principles., • Familiarity with raw materials, GLPs, GMPs, FDA guidelines, global regulatory requirements, and color cosmetics technologies., • 1–3 years of hands-on experience in cosmetic formulation, preferably including powders, • Experience working in a very fast-paced laboratory or R&D environment with shifting priorities., • Proven ability to adapt to rapid project changes, evolving client requests, and urgent internal priorities., • Strong project management skills, with the ability to juggle multiple formulations simultaneously in a deadline-driven setting., • Proficiency in Word, Excel, SAP, DEVEX, and other relevant technical software., • Excellent written and verbal communication skills, including technical documentation, presentations, and client-facing communication., • Strong mathematical, analytical, and problem-solving capabilities., • Professional, organized, detail-oriented, and collaborative within a dynamic team environment. Job Benefits Health Insurance: Comprehensive medical, dental, and vision coverage Retirement Plans: 401(k) plan, often with company matching Life Insurance: Coverage for employees in the event of death or disability Paid Time Off (PTO): Vacation days, sick leave, and personal days Holidays: Paid company holidays and floating holidays Professional Development: Training programs and opportunities for career advancement Company Events: Team-building activities, social events, and company outings Employee Assistance Programs (EAPs): Confidential counseling and support services for personal and professional issues. EEO Intercos Group is committed to creating a diverse and inclusive workplace where everyone is valued and respected. We believe that a wide range of perspectives and experiences enhances our innovation and success. We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or any other legally protected status. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to any of these characteristics. We are dedicated to providing a work environment that is free from discrimination and harassment and promotes equal opportunity for all.

Description The Medical Assistant I provides clinical office support to physicians and surgeons and performs patient care and administrative duties necessary to deliver quality patient care. Responsibilities • Fulfills patient care responsibilities as assigned which may include: performing venipuncture and/or EKGs, checking schedules and organizing patient flow; accompanying patients to exam/procedure room, assisting patients as needed with walking, transferring and dressing, as well as collecting and processing specimens and point of care testing, preparing for exam, etc. Assists physicians with various procedures, takes vital signs, relays instructions to patients and or families; answers calls and provides pertinent information., • Fulfills clerical responsibilities as assigned which may include: sending and receiving patient medical records; obtaining lab/x-ray reports, hospital notes, referral information, etc. Completing forms and requisitions as needed, managing charts to ensure information is completed and filed appropriately. These responsibilities may be carried out using the electronic medical record (EMR) system or manually as necessary., • Enters orders into the electronic medical record (EMR) system or prepares prescription refill requests on behalf of the physician for the review and approval by the ordering physician., • Inventories, orders or re-stocks medical supplies as applicable., • Provides set-up of examination room and instruments in accordance with proper sterilization techniques established by hospital and infection control policies., • Maintains logging system as required for refrigeration of medications, point of care testing, sterilization process, crash cart, point of care testing or others as needed., • Checks expiration dates on all medications and medical supplies disposing appropriately as per institution policy., • Maintains a safe, secure, and healthy work environment by following standards and procedures; complies with legal regulations., • Complies with established personal protective equipment requirements necessary for protection against exposure to blood and other potentially infections body fluids, chemical disinfectants, radiation and other hazardous substances., • Assists in the maintenance of medical charts (filing, Op Reports, test results, home care forms)., • May schedule surgeries/procedures or work in conjunction with Surgical Coordinator verifying times with patients; preparing charts, pre-admissions and consent forms as necessary., • May be required to perform proficient phlebotomy duties., • May perform appointment scheduling and registration for patients as well as updating patient demographic and insurance information., • May maintain, adjust and confirm patient office schedule., • May check and verify and update insurance information utilizing internal or web sources., • May perform and verify pre-certification for procedures as necessary., • Performs other duties as assigned. Qualifications • High School Diploma/GED with completion of Training Certificate from an approved Medical Assistant certificate course. Certified Medical Assistant preferred., • Three to nine months of healthcare experience preferred. Venipuncture and EKG skills required, • Certificate of Medical Assistant training or equivalent, • BCLS certification – Required Issuing Authority: AHA Compensation The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $23.9808 - $31.4572 Hourly. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits. Employer Description Strength through Unity and Inclusion The Mount Sinai Health System is committed to fostering an environment where everyone can contribute to excellence. We share a common dedication to delivering outstanding patient care. When you join us, you become part of Mount Sinai’s unparalleled legacy of achievement, education, and innovation as we work together to transform healthcare. We encourage all team members to actively participate in creating a culture that ensures fair access to opportunities, promotes inclusive practices, and supports the success of every individual. At Mount Sinai, our leaders are committed to fostering a workplace where all employees feel valued, respected, and empowered to grow. We strive to create an environment where collaboration, fairness, and continuous learning drive positive change, improving the well-being of our staff, patients, and organization. Our leaders are expected to challenge outdated practices, promote a culture of respect, and work toward meaningful improvements that enhance patient care and workplace experiences. We are dedicated to building a supportive and welcoming environment where everyone has the opportunity to thrive and advance professionally. Explore this opportunity and be part of the next chapter in our history. About the Mount Sinai Health System: Mount Sinai Health System is one of the largest academic medical systems in the New York metro area, with more than 48,000 employees working across eight hospitals, more than 400 outpatient practices, more than 300 labs, a school of nursing, and a leading school of medicine and graduate education. Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time — discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. Through the integration of its hospitals, labs, and schools, Mount Sinai offers comprehensive health care solutions from birth through geriatrics, leveraging innovative approaches such as artificial intelligence and informatics while keeping patients’ medical and emotional needs at the center of all treatment. The Health System includes more than 9,000 primary and specialty care physicians; 13 joint-venture outpatient surgery centers throughout the five boroughs of New York City, Westchester, Long Island, and Florida; and more than 30 affiliated community health centers. We are consistently ranked by U.S. News & World Report's Best Hospitals, receiving high "Honor Roll" status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology. New York Eye and Ear Infirmary of Mount Sinai is ranked No. 12 in Ophthalmology. U.S. News & World Report’s “Best Children’s Hospitals” ranks Mount Sinai Kravis Children's Hospital among the country’s best in several pediatric specialties. The Icahn School of Medicine at Mount Sinai is ranked No. 11 nationwide in National Institutes of Health funding and in the 99th percentile in research dollars per investigator according to the Association of American Medical Colleges. Newsweek’s “The World’s Best Smart Hospitals” ranks The Mount Sinai Hospital as No. 1 in New York and in the top five globally, and Mount Sinai Morningside in the top 20 globally. Equal Opportunity Employer The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization.

Client Overview Our client is a consumer products company that specializes in cosmetics and personal care products. They are currently seeking a Chemist (Cosmetics) who can operate in a very fast-paced environment. Salary/Hourly Rate $55k - $65k Position Overview The Chemist (Cosmetics) will lead technical efforts in formulating, innovating, and scaling powder-based and/or color cosmetic products, with occasional support for emulsion and anhydrous developments. This role requires collaboration across teams in a fast-paced setting. Responsibilities Of The Chemist (Cosmetics) • Develop and refine cosmetic formulations, including powder-based, anhydrous, and emulsion systems, in alignment with project specifications and customer objectives., • Execute formulation projects from concept through development, including new product innovation, shade matching and extensions, reformulation, and performance enhancement., • Identify and evaluate raw materials, formulation approaches, and processing methods to improve product aesthetics, functionality, stability, and manufacturability., • Work with customers to establish product requirements, address formulation challenges, assess product attributes, and recommend solutions that meet technical and brand expectations., • Communicate development progress and technical findings through laboratory demonstrations, prototype reviews, written reports, and presentations to internal and external stakeholders., • Monitor developments in cosmetic science, ingredient technologies, and market trends, particularly those related to powders, emulsions, and anhydrous formulations., • Partner with teams across marketing, manufacturing, quality, regulatory, packaging, and corporate research to support successful product development and commercialization., • Perform initial stability assessments on new and existing formulations, interpret results, and adjust formulas as needed to improve product consistency and durability., • Maintain and update formulation records within DEVEX, ensuring compliance with established procedures, documentation requirements, BPM communication practices, and R&D standards., • Support alignment of global research practices by coordinating with corporate applied research teams on testing procedures, technical data, and standardized development processes., • Maintain complete and accurate laboratory notebooks, batch documentation, and project records, communicating project status and development progress to the direct supervisor., • Balance competing project deadlines and changing priorities while responding effectively to evolving customer needs and internal business requirements., • Assist with additional laboratory, research, and departmental activities as needed. Required Experience/Skills For The Chemist (Cosmetics) • Approximately 1-3 years of hands-on experience in cosmetic formulation, product development, or a related laboratory-based R&D function., • Foundational knowledge of cosmetic formulation principles, particularly powder technology, including pigments, binders, dispersions, and powder processing methods., • Understanding of emulsion and anhydrous formulation systems., • Familiarity with cosmetic ingredients, color cosmetics, and applicable laboratory and manufacturing practices, including GLP, GMP, FDA guidance, and international regulatory considerations., • Ability to work effectively in a fast-moving R&D setting where project requirements, deadlines, and priorities may change., • Strong organizational and project coordination skills, with the ability to oversee multiple formulation assignments concurrently., • Proficiency in Microsoft Word and Excel; familiarity with SAP, DEVEX, and other formulation or technical software., • Effective written and verbal communication skills, including the ability to document technical findings, present results, and communicate with customers., • Strong analytical reasoning, mathematical aptitude, troubleshooting ability, and attention to detail., • Collaborative and adaptable working style, with a professional approach to laboratory work and cross-functional partnerships. Preferred Experience/Skills For The Chemist (Cosmetics) • Experience developing color cosmetics, particularly pressed powders, loose powders, pigments, and other powder-based formulations., • Exposure to cosmetic product scale-up, manufacturing trials, or transferring laboratory formulations into production., • Familiarity with cosmetic stability testing, raw material evaluation, and formulation optimization to improve product performance and shelf life. Education Requirements • Bachelor's degree in Chemistry, Biology, Chemical Engineering, or another related scientific field is required. Benefits • Medical, dental, and vision coverage., • 401(k)., • Paid time off (PTO)., • Paid holidays., • Additional benefits available.

We are seeking a highly motivated contractor to support vaccine research through computational biology, multi-omics data integration, and AI-enabled research workflows. The contractor will develop analytical tools and data systems for bulk RNA-seq, single-cell RNA-seq, TCR sequencing, BCR sequencing, and host immune profiling datasets. The role will also contribute to the design and implementation of an AI-enabled, multi-agent research platform that helps scientists search, integrate, analyze, and reason across complex biological datasets, scientific literature, knowledge graphs, and vaccine research workflows. Key Responsibilities: • Integrate and analyze multi-omics datasets, including transcriptomics, proteomics, metabolomics, single-cell profiling, and immune repertoire data, to identify biomarkers and molecular signatures relevant to vaccine response, efficacy, and safety., • Demonstrate strong familiarity with state-of-the-art methods and tools for bulk RNA-seq, single-cell RNA-seq, TCR profiling, BCR profiling, and immune profiling data analysis., • Design AI-agent solutions that help researchers explore, query, integrate, analyze, and generate insights from multi-omics datasets and related scientific knowledge., • Build data pipelines and knowledge systems that allow AI agents to retrieve, summarize, connect, and reason across biological datasets, metadata, research workflows, and scientific literature., • Develop interfaces and APIs to support interaction with internal databases, cloud storage, bioinformatics pipelines, and external scientific resources., • Collaborate with computational biologists, data scientists, and software engineers to translate research needs into scalable AI solutions. Required Qualifications: • Master’s degree or Ph.D. in computational biology, bioinformatics, computer science, AI/ML, data science, immunology, or a related quantitative scientific field., • Experience analyzing multi-omics datasets for biomedical or vaccine research, such as genetics, bulk RNA-seq, single-cell RNA-seq, spatial omics, immune repertoire profiling, proteomics, or related data types., • Experience with biomarker discovery, immune-response analysis, or systems immunology, preferably in the context of vaccine, infectious disease, or immunology research., • Strong communication and collaboration skills with the ability to work effectively in a hybrid team environment. Preferred Qualifications: • Hands-on experience generating immunological insights from single-cell sequencing data is highly desirable., • Expertise in artificial intelligence, large language models, retrieval-augmented generation, agentic AI workflows, or multi-agent system architecture is highly desirable., • Experience building LLM-based applications, multi-agent AI systems, agent orchestration workflows, or autonomous research assistants. Strong software engineering skills in Python and modern AI development frameworks are preferred., • Ability to document code thoroughly to ensure reproducibility and clarity for collaborative projects.

Job Description Job Title: Environmental Planner / Environmental Scientist Location: Melville, NY Type: Direct Hire Compensation: $68,000.00 to $75,000.00 Hours: 40.0 hours per week Responsibilities • Assist in the management of environmental review projects and technical analyses from project initiation through completion. • Perform environmental and zoning regulatory analyses. • Prepare and oversee technical sections of Environmental Impact Statements (DEIS/FEIS), Environmental Assessments, and related environmental review documents. • Conduct environmental analyses involving natural resources, wetlands, water resources, ecological systems, land use compatibility, and cumulative impacts. • Coordinate and review technical studies prepared by subconsultants and subject matter experts. • Identify potential environmental impacts and develop practical mitigation strategies. • Support permitting and regulatory compliance efforts under applicable state and federal programs. • Prepare technical reports with appropriate exhibits, maps, and graphics. • Work directly with clients, municipal boards, regulatory agencies, and project teams. • Participate in public meetings and hearings and assist with responses to agency and public comments. • Mentor and supervise junior environmental staff and provide quality control review of technical work products. Requirements • Bachelor's degree in Environmental Science, Ecology, Environmental Policy, Geology, Environmental Engineering, or a related discipline; Master's degree preferred. • Minimum 3 years of relevant professional experience, 5 or more years preferred. • Demonstrated experience preparing or managing environmental review documents under SEQRA and/or NEPA; CEQR experience is a plus. • Strong understanding of New York environmental regulations, permitting processes, and environmental review procedures. • Experience coordinating multidisciplinary technical teams and managing project schedules and budgets. • Excellent technical writing, analytical, research, and organizational skills. • Experience presenting before municipal boards, agencies, or at public hearings is desirable. • Proficiency with Microsoft Office; experience with GIS and environmental data analysis tools is preferred. • Ability to manage multiple concurrent assignments in a collaborative consulting environment. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M- #LI- Ref: #558-Scientific

Description \n The Medical Assistant I provides clinical office support to physicians and surgeons and performs patient care and administrative duties necessary to deliver quality patient care. \n \n Responsibilities \n\n • Fulfills patient care responsibilities as assigned which may include: performing venipuncture and/or EKGs, checking schedules and organizing patient flow; accompanying patients to exam/procedure room, assisting patients as needed with walking, transferring and dressing, as well as collecting and processing specimens and point of care testing, preparing for exam, etc. Assists physicians with various procedures, takes vital signs, relays instructions to patients and or families; answers calls and provides pertinent information.\n, • Fulfills clerical responsibilities as assigned which may include: sending and receiving patient medical records; obtaining lab/x-ray reports, hospital notes, referral information, etc. Completing forms and requisitions as needed, managing charts to ensure information is completed and filed appropriately. These responsibilities may be carried out using the electronic medical record (EMR) system or manually as necessary.\n, • Enters orders into the electronic medical record (EMR) system or prepares prescription refill requests on behalf of the physician for the review and approval by the ordering physician.\n, • Inventories, orders or re-stocks medical supplies as applicable.\n, • Provides set-up of examination room and instruments in accordance with proper sterilization techniques established by hospital and infection control policies.\n, • Maintains logging system as required for refrigeration of medications, point of care testing, sterilization process, crash cart, point of care testing or others as needed.\n, • Checks expiration dates on all medications and medical supplies disposing appropriately as per institution policy.\n, • Maintains a safe, secure, and healthy work environment by following standards and procedures; complies with legal regulations.\n, • Complies with established personal protective equipment requirements necessary for protection against exposure to blood and other potentially infections body fluids, chemical disinfectants, radiation and other hazardous substances.\n, • Assists in the maintenance of medical charts (filing, Op Reports, test results, home care forms).\n, • May schedule surgeries/procedures or work in conjunction with Surgical Coordinator verifying times with patients; preparing charts, pre-admissions and consent forms as necessary.\n, • May be required to perform proficient phlebotomy duties.\n, • May perform appointment scheduling and registration for patients as well as updating patient demographic and insurance information.\n, • May maintain, adjust and confirm patient office schedule.\n, • May check and verify and update insurance information utilizing internal or web sources.\n, • May perform and verify pre-certification for procedures as necessary.\n, • Performs other duties as assigned.\n\n \n Qualifications \n\n • High School Diploma/GED with completion of Training Certificate from an approved Medical Assistant certificate course. Certified Medical Assistant preferred.\n, • Three to nine months of healthcare experience preferred. Venipuncture and EKG skills required\n, • Certificate of Medical Assistant training or equivalent\n, • BCLS certification – Required Issuing Authority: AHA\n\n \n Compensation \n The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $23.9808 - $31.4572 Hourly. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits. \n \n Employer Description \n Strength through Unity and Inclusion \n The Mount Sinai Health System is committed to fostering an environment where everyone can contribute to excellence. We share a common dedication to delivering outstanding patient care. When you join us, you become part of Mount Sinai’s unparalleled legacy of achievement, education, and innovation as we work together to transform healthcare. We encourage all team members to actively participate in creating a culture that ensures fair access to opportunities, promotes inclusive practices, and supports the success of every individual. \n At Mount Sinai, our leaders are committed to fostering a workplace where all employees feel valued, respected, and empowered to grow. We strive to create an environment where collaboration, fairness, and continuous learning drive positive change, improving the well-being of our staff, patients, and organization. Our leaders are expected to challenge outdated practices, promote a culture of respect, and work toward meaningful improvements that enhance patient care and workplace experiences. We are dedicated to building a supportive and welcoming environment where everyone has the opportunity to thrive and advance professionally. Explore this opportunity and be part of the next chapter in our history. \n \n About the Mount Sinai Health System: \n Mount Sinai Health System is one of the largest academic medical systems in the New York metro area, with more than 48,000 employees working across eight hospitals, more than 400 outpatient practices, more than 300 labs, a school of nursing, and a leading school of medicine and graduate education. Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time — discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. Through the integration of its hospitals, labs, and schools, Mount Sinai offers comprehensive health care solutions from birth through geriatrics, leveraging innovative approaches such as artificial intelligence and informatics while keeping patients’ medical and emotional needs at the center of all treatment. The Health System includes more than 9,000 primary and specialty care physicians; 13 joint-venture outpatient surgery centers throughout the five boroughs of New York City, Westchester, Long Island, and Florida; and more than 30 affiliated community health centers. We are consistently ranked by U.S. News & World Report's Best Hospitals, receiving high "Honor Roll" status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology. New York Eye and Ear Infirmary of Mount Sinai is ranked No. 12 in Ophthalmology. U.S. News & World Report’s “Best Children’s Hospitals” ranks Mount Sinai Kravis Children's Hospital among the country’s best in several pediatric specialties. The Icahn School of Medicine at Mount Sinai is ranked No. 11 nationwide in National Institutes of Health funding and in the 99th percentile in research dollars per investigator according to the Association of American Medical Colleges. Newsweek’s “The World’s Best Smart Hospitals” ranks The Mount Sinai Hospital as No. 1 in New York and in the top five globally, and Mount Sinai Morningside in the top 20 globally. \n \n Equal Opportunity Employer \n The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization. \n

Job Description Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: PR: $21-$23 per hr. Work Model: Onsite – onsite Hours: 6:00am to 2:30pm Overview Responsibilities • Performs analyses of Clinical Chemistry, Critical Care, coagulation and microbiology controls and reagents using various automated techniques in accordance with established quality standards and GMP requirements, • Perform automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product, • Interprets test results against specifications and decides if assays pass or fail, • Maintains documentation of all work performed in accordance with GMP requirements, • Performs product stability, proficiency, environmental testing and water system testing, • Responsible for routine preventive maintenance, general trouble shooting, general cleanliness and calibration of lab equipment, • Updates departmental SOPs and QC Monographs as directed, • Performs microbial testing per SOPs and QC Monographs, • Orders required laboratory supplies, reagents and other consumables, • Monitors proper storage conditions and expiration dates, • Disposal of hazardous and bio-hazardous materials, • Maintains retain samples in accordance with established procedures, • Maintains statistical process control charts and other tracking reports Requirements • Min. BS/BA Biology, Chemistry, or Medical Technology, • 3-6 months of research experience (could be academic, internship, co-op) or industry experience System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M-3 #LI-HM Ref: #558-Scientific

Job Description Job Title: Bench Scientist I Location: Pearl River, NY Type: Contract Compensation: $35-$40.22 Work Model: Onsite – onsite Hours: 40.0 hours per week Overview Leading pharmaceutical company looking for an experienced Bench Scientist I. Ideal candidates should have a bachelors degree with a minimum of 2–4 years of experience including hands-on experience with one or more of the following: ELISA, Neutralization assays, Luminex assays, Cell culture techniques, Immunology- or vaccine-related laboratory methods. Responsibilities • Perform immunological assays to evaluate immune responses to vaccine candidates, including: ELISA, Neutralization assay with ELISA, Luminex assays, Functional antibody assays, and Cell culture-based assays, • Conduct laboratory work in a BSL-2 environment while adhering to applicable safety and quality standards, • Analyze, document, and interpret experimental data to ensure accuracy, integrity, and timely reporting, • Maintain detailed laboratory records, electronic notebooks, and presentation materials, • Generate, characterize, and track critical reagents used in preclinical and translational vaccine studies, • Support assay optimization, troubleshooting, and continuous process improvements, • Collaborate with scientists and cross-functional teams to meet project objectives and timelines, • Contribute to data presentations, reports, and scientific discussions Requirements • Bachelor’s degree in Immunology, Virology, Biology, Microbiology, or a related life science field, • Minimum of 2–4 years of relevant laboratory experience in a research, biotechnology, pharmaceutical, or academic setting, • Hands-on experience with one or more of the following: ELISA, Neutralization assays, Luminex assays, Cell culture techniques, Immunology- or vaccine-related laboratory methods, • Strong understanding of immunology, virology, or vaccine development principles, • Proficiency with Microsoft Office (Excel, Word, and PowerPoint), • Strong organizational, documentation, and data analysis skills Preferred Qualifications • Experience supporting vaccine research or infectious disease programs, • Familiarity with preclinical or clinical immunogenicity studies, • Knowledge of assay development, validation, or troubleshooting, • Experience working within regulated laboratory environments and following data integrity requirements System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #558-Scientific

Job Description Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $22.00 to $23.00 Work Model: Onsite – onsite Hours: 6:00am to 2:30pm Responsibilities • Perform analyses of Clinical Chemistry, Critical Care, coagulation, and microbiology controls and reagents using various automated techniques in accordance with established quality standards and GMP requirements, • Perform automated and manual assays as detailed in departmental/plant SOPs and QC Monographs, including raw material, in-process, and finished product testing, • Interpret test results against specifications and decide if assays pass or fail, • Maintain documentation of all work performed in accordance with GMP requirements, • Perform product stability, proficiency, environmental testing, and water system testing, • Conduct routine preventive maintenance, troubleshooting, cleaning, and calibration of lab equipment, • Update departmental SOPs and QC Monographs as directed, • Perform microbial testing per SOPs and QC Monographs, • Order required laboratory supplies, reagents, and other consumables, • Monitor proper storage conditions and expiration dates of materials, • Dispose of hazardous and bio-hazardous materials following proper procedures, • Maintain retain samples according to established procedures, • Maintain statistical process control charts and other tracking reports Requirements • Bachelor's Degree in Biology, Chemistry, or Medical Technology, • 3-6 months of research experience (academic, internship, co-op) or industry experience, • Ability to perform automated and manual laboratory tests, • Strong documentation skills in accordance with GMP standards, • Ability to perform routine maintenance and troubleshooting of lab equipment, • Familiarity with SOPs and QC Monographs, • Excellent organizational and monitoring skills for storage conditions and expiration dates, • Knowledge of hazardous waste disposal procedures System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M- #LI- Ref: #558-Scientific

Job Description Job Title: Bench Scientist II Location: Pearl River, NY Type: Contract Compensation: $40.00 - $48.00/hr Work Model: Onsite Overview Join a collaborative biopharmaceutical research team where you'll support the development and optimization of innovative immunoassays through hands-on laboratory work. This contract opportunity is ideal for an early-career scientist or recent Master's graduate eager to build experience with ELISA/MSD platforms, assay development, and emerging lab technologies in a supportive, fast-paced environment. Responsibilities • Support laboratory based assay development activities by performing day to day bench work., • Run ELISA assays as part of evolving and novel method workflows (not a QC lab role)., • Follow experimental protocols and contribute to experiments by asking appropriate scientific questions., • Perform strong basic laboratory skills, including pipetting, buffer preparation, and general lab techniques and documentation., • Support assay development concepts such as antibody titration, optimization, and sub-saturating conditions., • Prepare and characterize reagents, including antibody biotinylation and HABA assay or equivalent techniques., • Assist with laboratory automation workflows (e.g., Hamilton, Integra, or similar systems) when applicable., • Use or contribute to LIMS / electronic lab notebook processes as part of experiment documentation., • Maintain accurate documentation using Microsoft Office (Excel, Word) as needed. Requirements, • Hands-on experience running ELISA assays., • Experience with MSD platform preferred (ELISA experience acceptable if MSD is not available)., • Strong basic laboratory skills including pipetting, buffer preparation, general lab techniques and documentation., • Ability to follow experimental protocols and ask appropriate scientific questions., • Bachelor's Degree with 2–4 years of relevant lab experience or recent Master’s graduates with translatable hands-on lab experience., • Comfortable working in a highly collaborative, supportive team environment., • Preferred / Plus: Experience with assay development concepts (e.g., antibody titration, optimization, sub-saturating conditions)., • Preferred / Plus: Experience preparing and characterizing reagents, including antibody biotinylation and HABA assay or equivalent techniques., • Preferred: Familiarity with laboratory automation (e.g., Hamilton, Integra, or similar systems)., • Preferred: Experience using or exposure to LIMS / electronic lab notebooks., • Preferred: Familiarity with AI tools (e.g., Copilot). System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #558-Scientific

Job Description Job Title: Laboratory Technician Location: Orangeburg, NY Type: Contract Compensation: $22.00 - $23.00 per hour Hours: Monday-Friday 7:30-4:00pm Responsibilities • Perform moisture testing using Lighthouse plasma method, • Conduct analyses of clinical chemistry, critical care, plasma testing, coagulation, and microbiology controls and reagents using automated techniques in accordance with quality standards and GMP requirements, • Perform automated and manual assays as detailed in departmental/plant SOPs and QC Monographs for raw material, in-process, and finished product testing, • Interpret test results against specifications and determine whether assays pass or fail, • Maintain documentation of all work performed in accordance with GMP requirements, • Perform product stability, proficiency, environmental testing, and water system testing, • Conduct routine preventive maintenance, general troubleshooting, general cleanliness, and calibration of lab equipment, • Update departmental SOPs and QC Monographs as directed, • Perform microbial testing per SOPs and QC Monographs, • Order required laboratory supplies, reagents, and other consumables, • Monitor proper storage conditions and expiration dates of materials, • Dispose of hazardous and bio-hazardous materials following proper procedures, • Maintain retain samples in accordance with established procedures, • Maintain statistical process control charts and other tracking reportsRequirements, • Bachelor's Degree in Biology, Chemistry, or Medical Technology, • 3-6 months of research experience (academic, internship, co-op) or industry experience, • Ability to perform automated and manual laboratory tests, • Strong documentation skills in accordance with GMP standards, • Ability to perform routine maintenance and troubleshooting of lab equipment, • Familiarity with SOPs and QC Monographs, • Excellent organizational and monitoring skills for storage conditions and expiration dates, • Knowledge of hazardous waste disposal procedures System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M- #LI-Ref: #558-Scientific

Work Flexibility: Hybrid What you will do: As a Portfolio Manager on Stryker's Trauma team, you will help compile and evaluate research on customer needs in the market or segment and translate those needs into specifications for future generation products. Conduct market, competitive, and customer research using qualitative and quantitative data to identify industry trends, customer needs, and product opportunities. Translate product features, benefits, and customer insights into compelling value propositions and messaging strategies. Collaborate cross-functionally throughout the New Product Development Process (NPDP) to evaluate opportunities, support business objectives, and drive successful product launches. Build and maintain financial business case models to support product development investments, forecasting, pricing strategies, and return-on-investment analyses. Leverage organizational capabilities and strategic assets to maximize new product development, launch planning, and lifecycle management efforts. Partner with Clinical Affairs and Product Marketing to define evidence-generation strategies, develop publication plans, and ensure messaging aligns with clinical and scientific data. Evaluate customer acquisition and retention opportunities, including potential sources of new volume, market expansion strategies, and associated financial tradeoffs. Develop pricing strategies that align with overall marketing objectives, brand positioning, and business goals. Partner with Product Marketing and commercial teams to develop and execute product launch plans, sales enablement tools, channel communications, and marketing resources that drive market adoption. Execute product lifecycle management (PLCM) strategies to support long-term business growth and product performance. What you need: Required: Bachelor's degree, 4+ years of work experience Ability to be onsite at our Mahwah, NJ office 3x a week Preferred: MBA, 1+ years medical device or marketing experience preferred United States of America Pay Ranges: US20: $107,200 - $178,600 USD Annual View the U.S. work location and transparency guide to find the pay range for your location. Travel Percentage: 30% Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.

About Us Before applying for this role, please read the following information about this opportunity found below. Imagine the innovation and expertise behind the world’s leading cosmetic brands, brought to you by a distinguished Italian company with a legacy of excellence. Since 1972, Intercos Group has been at the forefront of color cosmetics, pencils, nail polish, skincare, and personal care products. We pride ourselves on being the only cosmetics manufacturer that combines top-tier quality and advanced technology with a global reach and a personalized touch. With 16 commercial offices and 16 production facilities across 12 countries, Intercos Group brings a local approach to a global stage. We continually set the standard for beauty, crafting exceptional product lines for brands worldwide. As one of the largest suppliers in the cosmetics industry, we are a leading force in the research, development, and production of beauty products, shaping the future of the industry with every season. Position Summary The Chemist is responsible for all technical activities related to new and existing formulation, innovation and 1st production scale-up of new formulations in Congers, NY. Essential Functions • Lead formulation and development of powder-focused cosmetic products while also formulating and supporting development of emulsion and anhydrous technologies as project needs arise., • Facilitate end-to-end development for assigned projects, including innovation, line extensions, reformulations, and performance upgrades across powder, emulsion, and anhydrous categories., • Identify and integrate new or improved raw materials, formulation technologies, and processing methods to elevate product performance while respecting constraints such as cost targets, regulatory requirements, and client blacklists., • Collaborate directly with clients to define formulation targets, troubleshoot issues, and deliver technical solutions aligned with brand expectations., • Provide technical support through clear verbal communication, written documentation, and formal presentations to internal teams and external customers., • Conduct proactive research to scout emerging concepts, advanced materials, new texture formats, and global innovation opportunities relevant to powders, emulsions, and anhydrous formulations., • Partner cross-functionally with Marketing, Manufacturing, Quality, Regulatory, Packaging, and Corporate Applied Research to ensure alignment, • Monitor preliminary product stability for new and existing formulations., • Manage multiple concurrent projects in a high-speed, deadline-driven environment, providing frequent updates to managers and stakeholders., • Execute all formula creation, customization, and documentation within DEVEX, ensuring compliance with SOPs, BPM communication standards, and Intercos development protocols., • Support global standardization efforts by collaborating with Corporate Applied Research to harmonize processes, testing methods, and technical databases., • Maintain organized laboratory notes, batch records, and project documentation, reviewing all activities with the direct supervisor., • Perform additional responsibilities as required. Job Qualifications • Bachelor’s Degree in a Scientific Discipline such as Chemistry, Biology, Physics, or related field., • Understanding of cosmetic formulation science, with emphasis on powder technology (e.g., pigments, binders, dispersions, powders processing)., • Working knowledge of emulsion and anhydrous formulation principles., • Familiarity with raw materials, GLPs, GMPs, FDA guidelines, global regulatory requirements, and color cosmetics technologies., • 1–3 years of hands-on experience in cosmetic formulation, preferably including powders, • Experience working in a very fast-paced laboratory or R&D environment with shifting priorities., • Proven ability to adapt to rapid project changes, evolving client requests, and urgent internal priorities., • Strong project management skills, with the ability to juggle multiple formulations simultaneously in a deadline-driven setting., • Proficiency in Word, Excel, SAP, DEVEX, and other relevant technical software., • Excellent written and verbal communication skills, including technical documentation, presentations, and client-facing communication., • Strong mathematical, analytical, and problem-solving capabilities., • Professional, organized, detail-oriented, and collaborative within a dynamic team environment. Job Benefits Health Insurance: Comprehensive medical, dental, and vision coverage Retirement Plans: 401(k) plan, often with company matching Life Insurance: Coverage for employees in the event of death or disability Paid Time Off (PTO): Vacation days, sick leave, and personal days Holidays: Paid company holidays and floating holidays Professional Development: Training programs and opportunities for career advancement Company Events: Team-building activities, social events, and company outings Employee Assistance Programs (EAPs): Confidential counseling and support services for personal and professional issues. EEO Intercos Group is committed to creating a diverse and inclusive workplace where everyone is valued and respected. We believe that a wide range of perspectives and experiences enhances our innovation and success. We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or any other legally protected status. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to any of these characteristics. We are dedicated to providing a work environment that is free from discrimination and harassment and promotes equal opportunity for all.

Job DescriptionSummary: The Medical Monitor Contractor will serve as a critical member of the clinical team, responsible for clinical data review, safety surveillance, and medical oversight activities supporting interventional clinical studies. This role requires a medically qualified professional with strong clinical judgment, prior medical monitoring experience, and the ability to critically evaluate safety and efficacy data in a fast-paced research environment. The successful candidate will contribute to ensuring the integrity, quality, and timely review of clinical trial data while supporting study teams with safety assessments, data interpretation, and operational activities. Roles & Responsibilities: • Clinical Data Review & Medical Monitoring, • Serve as a clinical team member responsible for ongoing data review and medical monitoring activities., • Verify participant eligibility based on medical history and protocol requirements., • Apply protocol-defined study criteria to assess data relevant to safety, tolerability, immunogenicity, efficacy, and other study endpoints., • Review serious adverse events (SAEs) and non-serious adverse events (AEs), ensuring accurate medical assessment and documentation., • Draft, review, and respond to site queries related to safety and clinical data., • Ensure accurate and timely reconciliation of safety data., • Review reactogenicity and other safety-related data captured in eDiaries, EDC systems, and other clinical databases to ensure compliance with protocol requirements., • Safety Oversight, • Support aggregate safety data review and interpretation., • Assist in the preparation and management of safety narratives., • Participate in safety surveillance activities and safety review meetings., • Contribute to safety presentations and PowerPoint development for internal and external stakeholders., • Support safety narrative authoring workflows and related documentation processes., • Study Support Activities, • Conduct literature reviews and medical research as needed., • Support data cleaning and data quality initiatives., • Review training materials and study documentation., • Assist with study startup, study conduct, and operational activities based on prior experience., • Contribute to protocol reviews, informed consent document reviews, feasibility assessments, and study-related medical input., • Support eDiary design and review activities when applicable., • Collaboration & Team Support, • Work closely with clinicians, study leadership, and cross-functional clinical teams., • Provide medical expertise to support study execution and data quality., • Be available during standard business hours and work the agreed-upon schedule., • Perform additional study-related responsibilities as assigned. Required Qualifications: • Medical Degree (MD, DO, MBBS, or equivalent)., • Minimum of 2 years of independent clinical practice experience post-residency., • Minimum of 2 years of medical monitoring experience within clinical research., • Experience reviewing safety data, including serious and non-serious adverse events., • Experience supporting interventional clinical trials within the last 3 years., • Strong understanding of clinical trial design, conduct, and execution., • Ability to critically evaluate complex medical and scientific information., • Experience reviewing clinical data involving pediatric, adult, and obstetrical populations., • Proficiency with Microsoft Word, Excel, and PowerPoint., • Excellent written and verbal English communication skills., • Ability to work independently and adapt in a fast-paced environment., • Preferred Qualifications:, • Previous experience supporting Pharmaceutical clinical studies or familiarity with large pharmaceutical company processes., • Vaccine clinical trial experience., • Experience in infectious diseases, infection control, or related therapeutic areas. Note: This role does not include interactions with regulatory authorities and does not involve direct contact with study site staff.