Research assistant jobs in Franklin, NJ

Onsite in 909 River Road Piscataway, NJ 08854 Monday - Friday, 8am - 4pm (with some flexibility) Reason for request: Lab development, stability, data integration/analysis work JOB DESCRIPTION: Perform appropriate Lab practices and procedures for making product formulation and testing of products. Follow product stability protocols. Maintain, monitor, validate and calibrate lab equipment, as necessary. Prepare reports, collect data analysis, and communicate progress and completion of tests to leadership. Maintain good record keeping habits. Responsibilities include: Lead the development and implementation of new toothpaste formulas for North America - under the hello and Tom's of Maine brands. Be the R&D point of contact for commercial teams for hello and Tom's key innovation. Lead experimental designs to help identity launch formulations and production processes. Make lab and pilot batches of formulations for stability testing and customer sampling. Support Pilot Plant batches by preparing batch sheets, requesting raw materials, pre-weighing materials and batch execution. Support plant trial batches at various North America locations as needed. Manage multiple stability studies at the lab, pilot and plant scale, working with support groups (analytical, flavor, micro, etc) to deliver samples and follow up on results. Create/maintain all required R&D documentation to ensure flawless, high quality commercialization. This may include R&D project timelines, formula databases, tech transfer checklists, proof of claims documents, registration documents, NODs, change control documents and technical justifications. Manage independent projects and collaborate with cross-functional teams, leveraging diverse perspectives to achieve key project goals and influence beyond your network Create and maintain all required documentation under GMP/GLP per FDA/ICH guidelines as required. Validate new raw material suppliers and packaging as required. Maintain a clean and organized working environment. Work on multiple tasks with changing priorities. Make day-to-day recommendations and escalate issues regarding formula development. Stay abreast of supplier and competitor's new developments. Abide by and follow all company standard operating procedures (SOPs) including those for product development, regulatory and safety. Deliver effective presentations of technical data and project status. Required Qualifications Bachelor's or MS Degree in Chemistry, Chemical Engineering, Biochemistry, Food Science or related fields. 4+ years of experience developing and/or implementing consumer products. Experience scaling up formulations from the lab through pilot or manufacturing scale. Technical understanding of related chemistry and science (for example: active deliveries, emulsions, surfactants, rheology, liquid chemistry) Strong knowledge of ingredient chemistry to be able to understand how the interdependencies and interactions of raw material components affect formulation and process performance Able to multi-task and coordinate various simultaneous projects Strong oral and written communication skills Self-motivated but able to work well within a team environment Knowledge of cGMP /GMP and GLP Excellent computer skills (MS Office, Google suite, SAP, etc.) Preferred Qualifications Knowledge of equipment and procedures for making oral care formulations Experience running stability studies for OTC/Drug products Experience & understanding of producing formulations at the manufacturing scale. Experience with claim substantiation. Strong project planning and management experience Knowledge of Regulatory environment in North America and across the globe Knowledge of ICH/FDA guidelines for stability and testing of new drug products Other Required Experience/Qualifications: Previous laboratory experience preferred. Must have hands-on experience with laboratory instruments. Must be able to learn new procedures in a short period of time. Must be able to follow SOPs and obtain reliable and accurate data. Must be able to document data consistently and accurately. Must be able to perform routine tasks daily

Akkodis is seeking a (Microbiology Laboratory Technician -(Laboratory /Research Associate, Cell Culture & Microbiology) for a contract job in Raritan NJ. Pay Range: $48/hr - $49/hr. The rate may be negotiable based on experience, education, geographic location, and other factors. Position: Microbiology Laboratory Technician -(Laboratory /Research Associate, Cell Culture & Microbiology) Location :: Raritan NJ, Onsite Contract : 6 Month+ EXPERIENCE Required: 2-3 years Role and Responsibilities Handling of various mammalian cell lines or bacteria, maintaining their growth, and expanding them as required for specific in vitro experiments to evaluate various wound healing products. Perform routine microbiological techniques (bacterial growth, streaking, spreading, plating and colony count etc.) Perform routing histology such as embedding, sectioning staining (immunohistochemistry, HE or immunocytochemistry) of animal and human tissue, and performing light fluorescence microscopy Perform various assays like ELIZA or PCR Maintain lab equipment calibration and ordering of lab consumables and keeping the lab compliant with EHS regulations Perform statistical analysis of in-vitro studies and prepare scientific presentations. If needed, collaborate with internal associates to develop, and validate in-vitro and ex-vivo assays for wound healing. Preferred: Minimum 2-3 years of hands-on laboratory work experience especially in cell (mammalian) culture and microbial culture Pre-clinical experience Performing studies independently or in a team, developing test methods and SOPs Good documentation practices, including writing test protocols, generating final reports, and documenting meeting minutes. Experience with multidisciplinary projects that require interfacing with different scientific disciplines (microbiology, material science, chemistry) Availability to work on weekends for cellmicrobial culture maintenance. Education: Bachelor's Degree. Equal Opportunity Employer/Veterans/Disabled Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit ****************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: · The California Fair Chance Act · Los Angeles City Fair Chance Ordinance · Los Angeles County Fair Chance Ordinance for Employers · San Francisco Fair Chance Ordinance

LIGHTERA has one of the longest and most respectable corporate lineages in American business, which goes back to Alexander Graham Bell and the invention of the telephone more than a century ago. We have a proven track record of being first in the industry with application specific fibers, optical connectors, ribbon cables, erbium doped fibers, Raman fiber lasers, fiber gratings and more. Our mission is to provide leading optical innovations and solutions by designing, manufacturing and supplying the best optical fibers, fiber cable and components and devices for our customers, with exceptional service that creates value for our shareholders, customers and employees. To do so, we must continue shaping the future of optical fiber technology by applying the best minds to the challenges our customers will continually face. We currently seek a Optical Fiber Research Intern to help support Lightera Laboratories in our Somerset, NJ location. Lightera Laboratories is pursuing new product development in fiber optics for sensing and medical devices. As part of this work, characterization of next generation fiber optics is required. Lightera Laboratories is seeking a summer intern interested in a mix of hands-on lab work, lab automation, and data analysis. The intern will assist Lightera Laboratories researchers in designing and testing next generation fiber optic components. The successful intern candidate will have demonstrated solid analytical abilities, initiative, and hands on experience in courses or other lab settings. Key qualifications: * Currently working toward a degree in a science and engineering-related field. * Familiarity with optics * Familiarity with programming in C, python and Matlab. * Lab experience with optics preferred * Passion and motivation to solve problems * Strong analytical ability, including use of AI. * Effective written and verbal communication skills * Proficiency with MS Office Teams, Outlook, Word, Powerpoint, and Excel * Discretion when working with confidential and proprietary information Essential duties and responsibilities * Assist Lightera Laboratories researchers in building test setups and using these to characterize new fiber components * Set up and align optics mechanics * Acquire and analyze data * Provide a final report-out presentation on project results Working at LIGHTERA means having the opportunity to realize ideas, experience innovation and discover new solutions for the future. In addition to our dynamic work environment, we offer competitive salaries and generous benefits programs, including medical, dental, tuition reimbursement and a matching 401(k) plan. Employees are expected to serve as role models for safe work practices and behaviors. This includes following established health and safety policies and procedures, maintaining a clean, organized work area, wearing, and properly storing all personal protective equipment (PPE), and actively engaging as a safety conscious worker with personal safety and wellness as a priority. If you'd like to be part of an energetic, world leader in optic fiber solutions, please apply through our Career portal at ******************************* Note: Only those candidates selected for the interview process will be contacted. About Lightera Lightera is a global leader in optical fiber and connectivity solutions, delivering innovative technologies that drive communication networks, data centers, and specialty photonics applications in the medical, industrial and defense markets. With a deep legacy of expertise in optical science, we provide high-performance solutions that enable faster, more reliable, and more sustainable connections for businesses, communities, and industries worldwide. Headquartered in Norcross, Georgia, U.S.A., Lightera operates with a global footprint, serving customers across telecommunications, enterprise, industrial, generative AI, data centers, 5G/6G, utilities, medical, aerospace, defense, and sensing markets. Lightera is part of Furukawa Electric Group, a multi-billion-dollar leader in optical communications. Lightera is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or status as an individual with a disability.

The Machine Learning Department invites applications for winter, summer, and fall 2026 internships. We have research projects covering many areas of machine learning. The internship will involve research and development of novel machine learning algorithms with applications in multimodal Large Language Models, AI for Science, real-time awareness, and healthcare. Our internships normally result in high-quality publications (***************************************************************** Minimum duration of the internships is usually 3 months, and the exact dates are flexible. We conduct research on various aspects of machine intelligence and reasoning, from the exploration of theoretical machine learning and new algorithms to applications in computer vision for real-time awareness and industrial digital twin, natural language understanding, and AI for Science. Ongoing projects focus on multimodal reasoning and planning, multimodal LLM, agentic generative AI, structured AI, workflow AI, AI safety, physics informed machine learning, and generative embodied AI, among others. Publishing is an integral part of our activities as a means for calibrating the quality of the research and to ensure staying at the forefront of technology. Application projects emphasize technologies that solve real world problems, and many of our research results have been and will be transferred into industry products.

Job Description The Inspired Company is a benefit corporation located in the Bedminster, NJ area. We believe saving lives requires disruptive new approaches, fearless leadership, and a renewed sense of urgency. We are looking to hire a dependable researcher to work on various company projects in an unpaid position. The researcher's duties include aligning methodologies with research goals, using a range of tools to acquire information and interpret data, writing up reports and presenting findings and schedules to management and other stakeholders, identifying trends and patterns, conducting fieldwork and tests when required, as well as protecting databases and confidential information. You should be able to deliver presentations and communicate effectively at all levels. To be successful as a researcher, you should be resourceful, and demonstrate excellent time management and patience. Outstanding researchers are passionate about their subject matter and able to meet strict deadlines. We are a powerhouse team of passionate advisors, experts, interns, and volunteers with vast knowledge in a variety of fields and skills. We at the Inspired Company strive for a cohesive team environment that will unlock powerful opportunities for mutual success among all parties involved. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin se, disability, age, veteran status, and other protected status as required by applicable law. Researcher Responsibilities: Interpreting research specifications and developing a work plan that satisfies requirements. Conducting desktop research, and using books, journal articles, newspaper sources, questionnaires, surveys, polls, and interviews to gather data. Analyzing and interpreting patterns and trends. Recording findings by taking written notes and using appropriate software. Maintaining and protecting electronic databases. Assisting management with budget and time schedules. Anticipating research issues and promptly resolving them. Promptly reporting any problems to the relevant stakeholders. Following a strict code of ethics and protecting any confidential information at all times. Writing proposals and delivering presentations when required. Researcher Requirements: Degree is preferred Proven experience in a research field. Sound understanding of research methodologies. Proficiency in google suite and documents. Strong statistical and mathematical aptitude. Strong problem-solving skills. Practical experience in database management. Attention to detail and exceptional written, verbal, and telephonic communication skills.

Inclusive Benefits We offer an inclusive and comprehensive range of benefits to our valued associates, including: Medical, Dental, Vision Benefits Disability Benefits Paid Parental Leave, Paid Family Leave, and Adoption Support Paid Time Off Retirement Savings Plan (401K) and Life Insurance Financial Solutions NMG Associates Core Discount of 30% Personal and Professional Development Opportunities For more information, please click “Our Benefits” section on our career site or reference the link here: https\://********************************** About Neiman Marcus Group Our legacy of innovation and culture of Belonging guide our roadmap for Revolutionizing Luxury Experiences. As a female-founded, female-majority organization that outpaces the U.S. population in racial and ethnic diversity, our people are at the heart of our progress, and we take great care to protect and empower them. We are committed to equal employment opportunity regardless of race, color, religion, sex, pregnancy, sexual orientation, gender identity and/or expression, marital status, age, national origin, disability, genetic information, veteran status, or any other status protected by federal, state, or local law. We are committed to providing reasonable accommodations during our Talent Acquisition process. If you have a disability and need assistance or an accommodation, please email us at *********************************. Other Compensation This position is eligible for commission in accordance with the terms of the Company's plan. Neiman Marcus Group is a relationship business that leads with love in everything we do-for our customers, associates, brand partners, and communities. Our legacy of innovating and our culture of Belonging guide our roadmap for Revolutionizing Luxury Experiences. Our brands include Neiman Marcus and Bergdorf Goodman. Your Role As a Client Advisor you will cultivate relationships with clients through elevated selling, exceptional customer service, and personal engagement while becoming their trusted style confidante. A Client Advisor will service clients who come into our store and digitally using the latest technology for outreach and selling. A Client Advisor can speak about fashion and trends with authority-both in person and digitally. This job is onsite at the specified location and will report to the Sales Manager. What You'll Do Maintain a customer-centric mentality. Demonstrate expert styling and brand knowledge, improve sales through Technology and Wardrobing. Understand how to showcase product differently based on if a client is remote or in-person Utilize selling tools and digital store technology to sell, use omni-channel and fleetwide inventory Achieve personal sales, client conversion and wardrobing goals Strategize own business to increase individual productivity through wardrobing, successful outreach and technology usage Utilize digital tools and social media to connect with clients and guide intentional traffic Create a positive work environment through collaboration What You Bring Motivated with an ability to set and achieve sales goal Experienced with technology and has experience selling to clients using digital tools Styling, fashion, and fashion retail experience Commission sales experience High School Diploma / equivalency required A flexible work schedule

At Genmab, we are dedicated to building extra[not]ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! Job Title Center for Outcomes Research, Real World Evidence and Epidemiology (CORE) Intern Why Genmab Our internship program provides interns with hands-on experience and relevant projects that directly align with our company's goals. Additionally, we believe our program provides a valuable opportunity to learn, thrive, and build a strong network. We encourage you to review our website to learn why we're always looking for smart, purpose-led candidates to play a role in our bold, extra[not]ordinary future. Job Overview The summer intern will have the opportunity to work on strategy and projects to demonstrate value of an oncology product approaching launch. They will gain exposure to HEOR, RWE and Medical Affairs teams at Genmab and will learn how HEOR can inform drug development and market access preparations at global and local level. What You'll Do * Conduct literature search/review re: unmet needs, treatment guidelines, impact of treatment on clinical, economic, patient reported outcomes. * Lead HEOR research projects providing input on study design, data analysis and results * Develop/Present (power point slides) on research-related topics to an extended or cross-functional team * Assist in preparations for medical planning and launch planning as appropriate * Assist in preparations for early scientific advice as appropriate. Required Qualifications, Capabilities and Skills * PhD student who has completed course work towards a PhD degree in Epidemiology, Economics, Public Health, Pharmaceutical Policy or a closely related area. * Strong analytical skills with the ability to translate key insights into strategy / tactics * Organized and detail-oriented * Excellent time management, verbal & written communication skills * Proficiency in SAS/R Programming and experience in working with claims and electronic health record datasets Preferred Qualifications, Capabilities and Skills * Experience in oncology therapeutic area * Experience using AI tools for HEOR analyses General Intern Information - Date/Location/Schedule Internships will take place June 2026-August 2026. This role will be based in Princeton, NJ, and operate on a required hybrid schedule - 3 days in the office and 2 days remote per week. What's next? Help us learn about you by submitting a complete and thoughtful application, which includes your resume. Your application and resume are a way for us to initially get to know you, so it's important to complete all relevant questions to ensure we have as much information about you as possible. Every application matters to us, and we'll carefully review each submission as quickly as possible to see if your qualifications align with the role. While we're unable to provide individual updates, rest assured that we're working diligently to move through the process efficiently. If you move forward in the process, you'll receive an email invitation to connect with us and dive deeper into this exciting opportunity. The final stage will bring selected candidates meeting directly with our hiring teams, where you'll have the chance to showcase your potential. We are committed to keeping you informed and will share decisions with all candidates as soon as we are able. We can't wait to see where this journey takes you! About You * You are genuinely passionate about our purpose * You bring precision and excellence to all that you do * You believe in our rooted-in-science approach to problem-solving * You are a generous collaborator who can work in teams with a broad spectrum of backgrounds * You take pride in enabling the best work of others on the team * You can grapple with the unknown and be innovative * You have experience working in a fast-growing, dynamic company (or a strong desire to) * You work hard and are not afraid to have a little fun while you do so! Locations Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you're in one of our office spaces or working remotely, we thrive on connecting with each other to innovate. About Genmab Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO) antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X. Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com).

Piper Companies is seeking a Analytical Research Associate to join a team in at a growing and innovative oncology cell therapy company in Branchburg, NJ. The foundation of this role is flow cytometry and ELISA-based work. Responsibilities: * Complete analytical testing and experimentation, with a focus on cell-based, PCR, flow cytometry, and ELISA assays--experience with Vi-Cell Blu a plus * Maintain, calibrate, and operate analytical equipment, along with laboratory material and reagent inventory * Document testing in accordance with laboratory requirements * Assist in laboratory and product failure investigations * Author technical and scientific documents including protocols, reports, and SOPs * Support technical transfer of methods to manufacturing for internal and external QC testing Qualifications: * 5+ years of experience working in a discovery role * Experience in cell-based, flow cytometry, and ELISA assays * Cell culture experience * Exposure to cell therapy products is preferred * Bachelor of Science in related field (Biology, Biotech, Biological Sciences) or Masters with 3+ years of experience Compensation for the QC Analytical Associate Scientist * Pay commensurate with experience: $47-53/HR * Comprehensive benefits package This job opens for applications on 11/17/2025. Applications will be accepted for at least 30 days from the posting date. #LI-NW1 #LI-ONSITEControl, Flow Cytometry, ELISA, Assays, Cell Culture, Cell Therapy, cGMP, QC Testing, Oncol

From the very beginning, we have been focusing on the science. We came together as a team of experts, committed to quality, driven by excellence, and dedicated to experimentation. Though we faced many challenges, we remained fearless in our research and rigorous in our thinking, pushing ourselves to work harder. However, what affected us the most was the enormous burden patient's bear and the difficulties they face, which drove us to think about what's next. We believe it is time to accelerate and expand that transformation. At Legend Biotech, we are excited to bring clinical trials to patients in our pursuit of a cure. While we are focusing on CAR-T in multiple myeloma, we firmly believe the prospects of cellular therapy stretch beyond just one disease or indication. The spark of hope is lit. At Legend Biotech, we are using that hope to ignite the future of CAR-T cell therapy. Job Description Role Overview: Legend Biotech is a clinical stage biopharmaceutical company focused on the discovery and development of novel cell therapies for oncology, immunology and infectious disease indications. We are currently seeking a talented and motivated candidate to join the R&D cell biology and immunology lab at US site. The successful candidate will contribute to the company's efforts to develop next-generation cell therapies in solid tumor malignancies. The successful candidate will have cell biology and immunology background, and expect to work in a collaborative cross-functional team environment, perform experiments, organize and analyze results, communicate effectively to support R & D teams. Major Responsibilities: Prepare cell banks of all the cell lines for R&D department usages Maintain biological reagents inventory stocks for R&D research. Maintain all laboratory instrument records. Comply with the correct procedures, policies, and health and safety regulations. Conduct laboratory tests, analyze results, and document your findings. Stay informed with the latest industry trends, techniques, and best practices. Document all activities, results and report to management as needed. Classify and label samples. Must also work well as a member of a collaborative team, be highly organized, have attention to detail and excellent time-management skills. Other duties assigned Qualifications Education: B.S. in bioscience field or cell biology and immunology Experience: · 0-2 year with B.S. Industry/academic experience in Cell Biology Key Capabilities, Knowledge, and Skills: Prior experience with cell culture and sterile technique Knowledge of cell biology and immunology Knowledge of lab procedures and understand the importance of maintaining a clean workspace by following all lab regulations for health and safety Flexibility to work on another lab support tasks Additional Information Legend Biotech USA Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech USA Inc. maintains a drug-free workplace.

Clinical Research Investigator (MD/DO) DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an Investigator for our site in Jersey City, NJ. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes. Responsibilities Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies. Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site. Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants. Interprets protocols and IB and participates in initiatives to strategize for patient recruitment. Carries out clinical evaluation and assessment of participants to ensure eligibility to enroll in studies. Ensures and protects the welfare and safety of participants through ethical conduct. Fulfills and complies with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations. Exercises meticulous attention to detail in documentation and patient care. Requirements Medical license (MD, DO) - New Jersey 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator) Bilingual Spanish a plus Flexible hours - schedule can be tailored as required.

KMK is a global data analytics and technology consulting company empowering leaders across the Life Sciences industries to make better data-driven decisions. Our data analytics and software platforms support data science, commercial operations, real world evidence, and cloud information management. We help to optimize business strategy and operations by delivering cutting edge analytics from the broadest set of data sources, combined with deep technical and domain expertise. We enable commercial excellence delivering analytical guidance to the field through SalesOps?, our cloud-based sales planning and operations platform. We are leaders in managing data using the latest cloud information management and big data technologies. We have more than 170 employees worldwide, are growing rapidly, and are proud to count a number of the top 10 global Life Sciences companies as our customers. We serve clients with a high-touch on-site and onshore presence, leveraged by a global delivery platform. Job Overview: We are currently seeking an experienced Health Economics & Outcomes Research (HE&OR) Associate. This position is responsible for the scientific and methodological aspects of all observational database analytics and evidence synthesis with minimal supervision. Job Description Provide consultation on all aspects of internal RWE databases studies/analyses including objectives, study design, data source identification, protocol development, statistical analysis and interpretation. Execute RWE studies/analyses by SAS based on claim database, EMR database, registry data and public used files. Generate high quality, readily interpretable deliverables (e.g., data tables, graphs, charts, study reports). Develop mock table shells, prepare specifications, and ensure quality control on analyses conducted by junior programmers. Effective manage and track all studies/analyses to ensure timelines are met and all stakeholders aware of project status. Effectively communicate research findings internally and externally, as appropriate (e.g., congresses, publications) Ensure latest methodologies and analytical techniques are implemented. Contribute to the continuing education of relevant line functions on RWE methodologies. Requirements Minimum MS in statistics, biostatistics, epidemiology, health economics and outcomes research, health policy, or similar. At least 2 years" hands-on experience in observational data studies. Professional programming skills with SAS. SQL and R programming experience are plus. Excellent interpersonal communication and study management skills. Ability to take detailed HE&OR study results and communicate them in a clear, non-technical manner to internal cross-functional teams, using language that resonates with the teams, while maintaining the integrity of key findings. Ability to work effectively in a constantly changing, diverse, and matrix environment. Ability to proactively identify new opportunities and solutions Strong working knowledge of the Microsoft Office Suite (Word, PowerPoint, Excel) Qualifications: Positive attitude/interested: Good candidates care about the result and how the result be used. They are willing to spend more time to explore more in addition to what is requested. They are able to readily take ownership of responsibilities Good problem-solving/critical thinking skills: Good candidates are able to understand problems clearly. They ask the right questions, break problems down into hypotheses and propose solutions in a coherent manner. Solid programming and analytical skills: Good candidates demonstrate competence in the application of statistical techniques and professional in programming which includes good programming habit and self-QC process. Good communication skills: Good candidates are able to take detailed study results and communicate them in a clear, non-technical manner to internal cross-functional teams, using language that resonates with the teams, while maintaining the integrity of key findings. Great at time and task management: Good candidates are able to estimate the amount of time needed to complete a task, communicate this to client clearly and deliver it on time. Quick learning capability/Self-motivated: Good candidates have the ability to learn new technologies on their own. Good team player Technical requirements: Minimum MS in statistics, biostatistics, epidemiology, computer science, or other quantitative analysis fields. Demonstrated competence in the application of statistical techniques, such as hypothesis testing, regression analysis, machine learning, etc.. Professional programming skills with SAS and SQL. R and/or Python programming experience is plus. Strong working knowledge of the Microsoft Office Suite (Word, PowerPoint, Excel). KMK Consulting, Inc. is a fast growing company with passionate, energetic, and dedicated people working in a dynamic and friendly environment. KMK Consulting, Inc. specializes in providing commercial operations support for the healthcare industry. We are hiring talented individuals who are interested in achieving individual and clients" success. KMK Consulting, Inc. offers: Great career opportunities and fast-paced development Competitive salary, vacation, self-directed 401(k) plan, life and health insurance benefits Centrally located office in a metropolitan atmosphere with convenient access to major transportation, highways and attractive amenities

Job Responsibilities: Assisting senior quantitative researchers to carry out quantitative strategy design, research and development of global futures, stocks and options market. Statistically analyzing large scale tick by tick financial data to extract alpha patterns. Qualifications: Advanced degrees from top universities, majoring in science and engineering, preferably Statistics, Mathematics, Computer Science, EE, and Physics. Have formal trainings of independent academic research. Programming skills: proficient in at least one of following programming languages - C/C++, Python/R. Mathematical basics: having a good understanding of data science, being critical in learning knowledge, understanding at least one of statistical modeling, machine learning, econometrics or optimization. Being fast, critical and reasonable in thinking. Good communicator, being rigorous, patient, and having a strong sense of teamwork. Highly motivated, and able to work in a fast-paced environment.

Vitalief partners with Sites, Sponsors, and CROs to streamline research operations, reduce costs, and accelerate breakthroughs that improve patient care. We bring deep clinical research expertise together with practical, results-driven consulting to help organizations operate more efficiently and achieve sustainable growth. THE ROLE We are seeking a highly motivated and detail-oriented PhD-level Graduate Research Assistant to support our client's dynamic neuroscience research laboratory. The successful candidate will contribute to a growing body of work focused on addiction, brain function, and behavioral neuroscience, playing a central role in manuscript development, grant preparation, data analysis, and general research operations. This position offers an exceptional opportunity for a doctoral candidate with a passion for translational research to gain hands-on experience in the scientific, analytical, and administrative aspects of academic research. COMPENSATION & WORK ENVIRONMENT Location: Onsite role in a collaborative and supportive research environment in Newark, NJ. Work Hours: Part-time, 20 hours/week (Flexible scheduling to accommodate academic commitments) Duration: 12-month contract Compensation: Competitive hourly rate commensurate with experience and academic standing. KEY RESPONSIBILITIES: Manuscript Development: Draft, edit, and prepare scientific manuscripts for publication in peer-reviewed journals, including literature reviews, data interpretation, and figure preparation. Grant Support: Assist in developing and editing grant proposals, supporting background research, and preparing preliminary data and figures. Data Analysis: Perform data cleaning, statistical analyses, and data visualization using appropriate software tools (e.g., SPSS, R, Python, MATLAB, or GraphPad Prism). Research Coordination: Support day-to-day lab activities, including documentation, database management, and coordination of research timelines. Literature Review: Conduct and synthesize current literature relevant to addiction and neuroscience to support ongoing studies and future grant submissions. Collaboration: Work closely with the Principal Investigator (PI), postdoctoral fellows, and other team members to advance the lab's research objectives. QUALIFICATIONS: Currently enrolled in a PhD program in Neuroscience, Psychology, Biomedical Sciences, or a related field. Prior research experience in neuroscience, addiction science, behavioral research, or related disciplines. Experience with academic/scientific writing and publication processes. Familiarity with grant writing (NIH or foundation-level preferred) is a strong plus. Background in statistical or computational data analysis methods. Excellent written and verbal communication skills; collaborative and comfortable working in a team-oriented lab environment. Self-directed and intellectually curious, professional, reliable, and responsive to feedback. Strong analytical and critical thinking abilities; high attention to detail and ability to manage multiple priorities. Proficiency in relevant software for data analysis, literature management (e.g., EndNote, Zotero), and document preparation. PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs. IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.

Job Title - Research Associate Co-op, Analytical Sciences Work Location - Cranbury NJ WuXi Biologics is a is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop, and manufacture biologics from concept to commercial manufacturing. WuXi Biologics' achievements are a direct result of the efforts made by our employees. We have built an extraordinary team motivated by our PROUD culture of Passion, Reward, Opportunity, Unity, and Determination. WuXi Biologics offers exciting job opportunities and careers around the globe. We currently employ over 12,000 people and provide services to more than 600 customers worldwide, including all the top 20 biopharmaceutical companies Job Summary We are looking for an enthusiastic co-op to join our Analytical Sciences team. This is a great opportunity for students interested in pharmaceutical or biotech R&D to gain practical lab experience and build a solid foundation in analytical method development and testing. Responsibilities * Assist in the execution of analytical tests, including but not limited to HPLC, CE, UV, and mass spectrometry. * Assist with sample preparation, buffer preparation, and instrument operation. * Perform data processing and documentation in compliance with laboratory standards. * Maintain accurate lab records and assist in generating technical reports. * Participate in equipment calibration, maintenance, and inventory management. * Work closely with scientists on assigned research or development tasks. Qualifications * Bachelor's or Master's student in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field. * Basic knowledge of chromatography, electrophoresis, and other analytical techniques. * Hands-on experience on lab work. * Experience with Empower or other data acquisition software. * Understanding of biologics development and regulatory expectations. * Basic knowledge of chromatography, electrophoresis, and other analytical techniques. * Strong organizational skills and attention to detail. * Effective communication and teamwork abilities. * Willingness to learn and good time management. * Proficient in Microsoft Office (Word, Excel, PowerPoint). The pay range for this position is $20-$30hr (based on education level) The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

Job Description: The Temporary Microbiology LaboratoryTechnician is responsible for performing general microbiological laboratoryduties as outlined below: Prepare microbiological media including QC sterilitychecks and media growth promotion testing Prepare specimens and materials, including cleaning theworkspace Perform microbiological testing of water in accordancewith standard procedures, using aseptic technique. Maintain accurate, up-to-date and concise laboratoryrecords General housekeeping/upkeep/cleaning of laboratory Monitor, clean, and perform calibration checks forlaboratory equipment and machinery Dish washing of laboratory glassware Autoclave waste Stock laboratory supplies and maintain laboratoryinventory Back up for Lab Analyst with respect to generalmicrobiological duties Work in a team environment under minimal supervision Participate in laboratory investigations Additional responsibilities as needed Skills/Experience/Education Bachelor\'s degree or equivalent in Microbiology/Biologyor working towards said degree, with Microbiology related coursework Minimum of 6-12 months experience in a Microbiologylaboratory, preferred Knowledge of GMP and aseptic techniques preferred Strong interpersonal skills Works well in a team environment Ability to work with minimal supervision Strong multi-tasking skills Precise, accurate and detail oriented

Siri InfoSolutions, Inc. is a private equity consortium firm providing IT staffing services to Fortune 500 clients across the US. We believe that it's an exceptional company - a company of people proud of the work they do and the solutions they provide. By understanding what drives our specialty industries, becoming involved in our communities on a professional and personal basis, following a disciplined process of identifying quality candidates, partnering with employers to understand their core business and their employment requirements, and delivering exceptional service, we achieve great results for all concerned. Professional Services: - Contract Staffing - Direct placements - Bench Sales - Application Development - Enterprise Resource Planning - Data Warehousing - Customer Relationship Management Siriinfo provides services to a wide spectrum of customers across verticals such as Banking, Financial Services, Healthcare, Human Resources, Telecom, Insurance, Hospitality, Retail & Distribution and Manufacturing. Serving multinational customers. Siri InfoSolutions reinforces its belief that the quality of our services can only be measured by the skills, performance and dedication of our employees. We will place only the very best candidates for our clients - candidates who are not only willing, but who possess the necessary skills to do the job effectively. Website ************************* Title : Lab Technician Location - Raritan, NJ Duration : 6+ Months Job Description: • Handling of various mammalian cell lines or bacteria, maintaining their growth, and expanding them as required for specific in vitro experiments to evaluate various wound healing products. • Perform routine microbiological techniques (bacterial growth, streaking, spreading, plating and colony count etc.) • Perform routing histology such as embedding, sectioning staining (immunohistochemistry, HE or immunocytochemistry) of animal and human tissue, and performing lightfluorescence microscopy • Perform various assays like ELIZA or PCR Maintain lab equipment calibration and ordering of lab consumables and keeping the lab compliant with EHS regulations • Perform statistical analysis of in-vitro studies and prepare scientific presentations. • If needed, collaborate with internal associates to develop, and validate in-vitro and ex-vivo assays for wound healing. Preferred: • Minimum 1-2 years of hands-on laboratory work experience especially in cell (mammalian) culture and microbial culture • Pre-clinical experience • Performing studies independently or in a team, developing test methods and SOPs Good documentation practices, including writing test protocols, generating final reports, and documenting meeting minutes. • Experience with multidisciplinary projects that require interfacing with different scientific disciplines (microbiology, material science, chemistry) • Availability to work on weekends for cellmicrobial culture maintenance. Additional Information All your information will be kept confidential according to EEO guidelines.

Job Description We are on the prowl for a Lab Technician to join our Mount Olive, New Jersey team at Symbiotic Research, a Tentamus North America company! If you are deeply passionate about science and enthusiastic about broadening your expertise, we invite you to apply today and become a vital part of our mission. How you will contribute as a vital part of our team: The Laboratory Technician will contribute to a world class laboratory by performing various laboratory duties under the direction of scientific staff which may include: Performing sample extraction, workup and pipetting. Adhere to all laboratory safety practices and follow applicable GLP regulations and government guidelines to conduct studies. Document all work performed following GDP principles. Communicate clearly with laboratory staff and scientists. Rely on SOPs and/or methods to perform the functions of the job. Prepare routine solutions; upkeep with laboratory cleanliness, organize all lab supplies to be easily accessible for all and provide laboratory maintenance. Maintain and calibrate the laboratory instruments as assigned. Support laboratory staff as needed. Position & Schedule Full-Time, 40 hours per week, Monday - Friday 8:30AM - 5:00PM or 9:00AM - 5:30PM with a 30-minute lunch break. Qualifications Our ideal candidate will be authorized to work in the United States indefinitely without restriction or sponsorship; have a BS in Biology preferred or related science field or experience working in a scientific laboratory setting; and an ability to work both independently and within a team. Other items include: Has knowledge of the use, maintenance, and/or calibration of most GLP equipment. Knowledge of laboratory operations. Must be able to work in a flexible environment, perform a variety of tasks and prioritize work. Ability to work under minimum supervision. Ability to implement scientific procedures and processes involved with residue, environmental fate and metabolism studies. Exhibit excellent oral and strong written communication skills. Self-sufficient in planning and executing daily responsibilities and the ability to tend to experimental details and attention to detail. Good computer skills and being adept with standard software (e.g. Windows, Excel, Word). Must be able to read, understand, and follow SOPs, policies and regulations, and provide general laboratory support. Required to frequently stand, walk, and sit. The employee must occasionally lift and/or move up to 40 pounds. What's in it for you? $16 per hour and a comprehensive and low-cost benefit plans (medical, dental, vision, disability, life insurance, HSA) Ample PTO and a matching 401k About Tentamus: Labs for Life . We are a global network of full-service accredited analytical laboratories providing crucial quality and safety analysis for clients locally, nationally, and beyond using proven methods of chemistry and microbiology. Many of the products you use and consume daily rely on Tentamus labs. With 20 labs in North America and growing (100 globally), we celebrate having talented diverse scientific and service-oriented professionals. Learn More: Tentamus Website | Symbiotic Research Website Job Posted by ApplicantPro

The Optical Networking and Sensing department invites applications for summer 2026 internships. We are seeking individuals with strong problem-solving skills and technical abilities, to work with us on applying cutting-edge AI and machine learning technologies to solve real-world problems in optical networking and intelligent sensing and make a practical impact on our future products and solutions for safety & security, smart city, infrastructure health monitoring, underwater surveillance, power & energy industry etc. Past projects include network digital twin, earthquake localization, transfer learning in EDFA gain models, adaptation and distillation of multi-modal foundation models, LLM application development, GPU computing, etc.

Job Description Vitalief partners with Sites, Sponsors, and CROs to streamline research operations, reduce costs, and accelerate breakthroughs that improve patient care. We bring deep clinical research expertise together with practical, results-driven consulting to help organizations operate more efficiently and achieve sustainable growth. THE ROLE We are seeking a highly motivated and detail-oriented Master's graduate to join our client's dynamic neuroscience research laboratory as a Graduate Research Assistant. The successful candidate will contribute to a growing body of work focused on addiction, brain function, and behavioral neuroscience, playing a central role in manuscript development, grant preparation, data analysis, and general research operations. This position offers an exceptional opportunity for a student with a passion for translational research to gain hands-on experience in the scientific, analytical, and administrative aspects of academic research. COMPENSATION & WORK ENVIRONMENT Location: Onsite role in a collaborative and supportive research environment in Newark, NJ. Work Hours: Part-time, 20 to 30 hours/week (Flexible scheduling to accommodate academic commitments) Duration: 12-month contract Compensation: Competitive hourly rate commensurate with experience and academic standing. KEY RESPONSIBILITIES: Manuscript Development: Draft, edit, and prepare scientific manuscripts for publication in peer-reviewed journals, including literature reviews, data interpretation, and figure preparation. Grant Support: Assist in developing and editing grant proposals, supporting background research, and preparing preliminary data and figures. Data Analysis: Perform data cleaning, statistical analyses, and data visualization using appropriate software tools (e.g., SPSS, R, Python, MATLAB, or GraphPad Prism). Research Coordination: Support day-to-day lab activities, including documentation, database management, and coordination of research timelines. Literature Review: Conduct and synthesize current literature relevant to addiction and neuroscience to support ongoing studies and future grant submissions. Collaboration: Work closely with the Principal Investigator (PI), postdoctoral fellows, and other team members to advance the lab's research objectives. QUALIFICATIONS: Master's degree in Neuroscience, Psychology, Biomedical Sciences, or a related field. Prior research experience in neuroscience, addiction science, behavioral research, or related disciplines. Experience with academic/scientific writing and publication processes. Familiarity with grant writing (NIH or foundation-level preferred) is a strong plus. Background in statistical or computational data analysis methods, including experience with SAS or SPSS, and some experience with AI models development. Excellent written and verbal communication skills; collaborative and comfortable working in a team-oriented lab environment. Self-directed and intellectually curious, professional, reliable, and responsive to feedback. Strong analytical and critical thinking abilities; high attention to detail and ability to manage multiple priorities. Proficiency in relevant software for data analysis, literature management (e.g., EndNote, Zotero), and document preparation. PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs. IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. Powered by JazzHR GiCn07JkZC