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Job Description The Clinical Trial Technician position is based within our Clinical Patch Testing department, and works with departmental management and the Principal Investigator in the implementation of clinical trials for patch testing protocols. Job Type: Full Time. Base Hours: 9:00AM - 6:00PM; OR 11:00AM - 8:00PM Monday through Friday MINIMUM QUALIFICATION REQUIREMENTS To perform this job, an individual must be able to perform each essential duty satisfactorily, and meet the educational and experience requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES • Review of protocols, test samples, inclusion/exclusion criteria, recruitment requirements and study schedule., • Implementation of all aspects of patch testing clinical trials, including compliance to Standard Operating Procedures, IRB approved protocols, Human Subject Protection, and regulatory requirements., • Perform CRF transcription and data entry into Excel platform., • Peer review trial data as required for accuracy, data integrity, and protocol compliance EDUCATION and/or EXPERIENCE • Must have High School diploma or GED, • Must have at least one year workforce experience COMMUNICATION SKILLS • Must have strong communication and interpersonal skills. OTHER KNOWLEDGE, SKILLS and ABILITIES • Must have initiative and problem solving / analytical skills and keen attention to detail, • Must be organized, flexible, and able to work independently., • Applicant should possess the ability to organize and maintain all clinical trial information for assigned projects and ensure adherence to established policies and procedures., • Must have the ability to work collaboratively and effectively with other clinical team members and physicians. PHYSICAL REQUIREMENTS On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch; talk, hear, and smell. This position requires the ability to lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials, and use of computer monitor screen frequently. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age or any other characteristic protected by law. Company DescriptionConsumer Product Testing Company is a worldwide leader in the contract laboratory testing of cosmetics, personal care, pharmaceuticals, medical devices and specialty chemicals. Since 1975, our staff has assisted clients with their testing needs from conception to completion. Our technical staff has extensive experience that is used to assist clients through each phase of the testing process. Our Quality Assurance and Regulatory staff monitors compliance to our internal SOPs and applicable regulations. We attribute our growth to our dedication to the needs of our clients. Well known for our superior customer service, we become an integral part of our clients' team, providing timely, reliable, accurate, and reproducible results.Consumer Product Testing Company is a worldwide leader in the contract laboratory testing of cosmetics, personal care, pharmaceuticals, medical devices and specialty chemicals. Since 1975, our staff has assisted clients with their testing needs from conception to completion. Our technical staff has extensive experience that is used to assist clients through each phase of the testing process. Our Quality Assurance and Regulatory staff monitors compliance to our internal SOPs and applicable regulations. We attribute our growth to our dedication to the needs of our clients. Well known for our superior customer service, we become an integral part of our clients' team, providing timely, reliable, accurate, and reproducible results.

Job Description Do you have solid tumor oncology nursing experience? Are you open to being trained in clinical research? Look no further! Our cutting-edge Cancer Center client in Northern NJ seeks experienced Oncology Nurses and is open to training for their clinical research team. Why Choose Us? • America's Best Hospitals: We're proud of our accolades and our commitment to excellence in patient care., • Patient Safety Excellence Award: Your safety matters to us! Perks You'll Love: • Comprehensive Medical, Dental, and Vision coverage, • Flexible Spending Account and Health Savings Account options, • Generous Paid Time Off (PTO), • 401k AND 403b Savings Plans, • Many other discounts and wellness programs Your Role: Making a Difference • Day Shifts, 4-10s: No weekends, no call, no holidays—just impactful work!, • Protocol Management: Ensuring protocols are shipshape! Submitting revisions, informed consents, and adverse events to the IRB., • Collaboration: Work closely with regulatory specialists, principal investigators, and sub-investigators to navigate protocol changes., • Feasibility Assessment: Investigate study protocols, evaluate feasibility, and outshine the competition., • Budget Wizardry: Review study budgets, balance standard care and research costs, and finalize with our budget coordinator., • Patient Recruitment: Spot potential study patients like a pro!, • Appointment Juggling: Coordinate interviews and appointments., • Patient-Centric Care: Customize care for our diverse patient population—age, culture, and all., • Effective Communication: Talk the talk with patients, parents, and caregivers. No jargon—just clear, compassionate communication. The Clinical Research Nurse is responsible for coordinating and overseeing clinical operations of a clinical trial and participates in assessing, planning, implementing, and evaluating patient care in clinical research studies. The Clinical Research Nurse carries out the research and works under the general supervision of the principal investigator responsible for the clinical trials. Your Profile: • NJ RN License: Current and valid (or ready to obtain)., • Oncology Passion: If you're an oncology nursing rockstar, our client will train you in clinical research., • BSN: Required. Ready to ignite your career? Apply now and let's make strides in cancer research together.

Job Description Title: Clinical Research Pharmacist Location: Secaucus, NJ (On-site required) Reports To: Executive Medical Director and Principal Investigator Company Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position Summary: We are seeking a licensed and detail-oriented Clinical Research Pharmacist to oversee all pharmacy-related activities in support of clinical trials conducted at Frontage Clinical Services. This role is essential in ensuring investigational drug products are handled, stored, dispensed, and documented in full compliance with sponsor requirements and regulatory standards. The successful candidate will be based onsite in Secaucus, NJ, and will contribute to developing pharmacy SOPs and manuals, while supporting cross-functional clinical teams throughout the study lifecycle. Responsibilities: • Develop, implement, and maintain procedures for investigational product (IP) inventory control, accountability, and reconciliation., • Ensure proper storage, handling, and labeling of IPs in accordance with protocol and regulatory standards., • Oversee preparation and dispensing of investigational study medications under sterile conditions when applicable., • Implement and enforce pharmacy access control; maintain documentation of authorized personnel., • Coordinate appropriate drug disposal procedures at the conclusion of each study., • Manage and document clinical drug packaging and labeling for specific protocols, as requested by the sponsor or Principal Investigator., • Collaborate with study teams to ensure pharmacy procedures align with sponsor protocols; review sponsor-specific medication handling requirements and escalate discrepancies if needed., • Provide input into protocol development for the clinical supplies section when requested., • Ensure all pharmacy records are audit-ready and compliant with GCP, ICH, and applicable regulations., • Bachelor of Science in Pharmacy (BS Pharm) or Doctor of Pharmacy (PharmD) from an accredited pharmacy school., • Current Registered Pharmacist (RPh) license in the State of New Jersey., • Minimum of 2 years’ experience as a licensed pharmacist; clinical research or investigational product handling experience strongly preferred., • Must be experienced with writing clinical research pharmacy manuals., • Must be able to work on-site in Secaucus, NJ., • Proficient in computer use to support pharmacy functions, including preparing and maintaining clinical documents, spreadsheets, and operational logs., • Strong understanding of GCP, FDA, and ICH guidelines as they relate to investigational product management., • Excellent communication, organization, and documentation skills., • Ability to work independently and collaboratively with cross-functional clinical teams. Salary: $150,000- $180,000 Benefits: • 401k Employer Match -Low PPO -High PPO -High PPO • Vision Insurance, • FSA (Medical, Dependent Care, and Commuter), • Short Term Disability, • Long Term Disability, • Life Insurance, • Generous PTO Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Job Description WHY VITALIEF? Vitalief is a trusted partner working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. We are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our clients’ mission to impact and save lives. Reasons to work for Vitalief: • You can actively contribute to our clients’ mission of advancing scientific discoveries that have the potential to change patients' lives for the better., • Our PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief employees., • We give everyone a seat at the table – we encourage innovation., • Life/work balance that includes 20 PTO (Paid Time Off) days plus 9 paid Holidays annually., • Other benefits include Company paid life insurance and short / long term disability coverage; 401K retirement program; Robust healthcare plans to choose from.Salary Range: Market competitive - based on experience level. Work Location: Work is 5 days per week on-site in Newark, NJ. Possibility of working one day remote per week after acclimated. Responsibilities: • Under supervision of clinical research leadership staff, the medical staff, and in collaboration with research nurse staff, performs protocol-specific tasks including patient screening, ordering tests, collecting specimens and study documentation of patient reported responses, relative to various Oncology trials., • Serves as a liaison (Communicating effectively) between the organization, investigators, members of the research team (i.e., physicians, nurses, hospital, and laboratory staff), and the research sponsors – to ensure that services are coordinated and delivered to patients in a timely manner., • Maintains research record (e.g., patient consent, eligibility, Case Report Forms (CRF), registration confirmation, corresponding source documents, etc.) for all patients enrolled in Oncology trials., • Participates in site preparation for trials including protocol feasibility, preliminary study budget, startup meeting preparation, training staff, and preparation of IRB applications and preparation of regulatory documents, study documents and forms., • Schedules and conducts trial visits by informing patients and coordinating procedures per protocol., • Assesses and triages study patients appropriately for serious/unexpected adverse events (SAE), reports and records adverse events according to all applicable regulation and study protocol., • Assists patients in understanding their diagnosis, treatment options, and the resources available including educating eligible patients about appropriate clinical research studies and technologies.Required Skills:, • Bachelor’s Degree required., • Minimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and reported within reporting deadlines outlined in the protocol., • Oncology clinical research experience is a huge plus., • Strong working knowledge of current Code of Federal Regulation and Good Clinical Practice guidelines., • Compassionate personality and ability to interact with patients in a clear and confident manner., • Ability to work on several trials concurrently – can demonstrate versatility, “can do” attitude, and possess strong organizational, time management and prioritization skills., • Ability to work collaboratively with all team members (i.e., physicians, nurses, hospital, and laboratory staff) to ensure that services are coordinated and delivered to patients in a timely manner., • Needs to be communicative and responsive and know when to escalate and communicate issues to management., • Capable of independent decision-making, and able to thrive in a fast-paced environment working on multiple clinical trials concurrently., • Must have strong Microsoft Office skills. 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. #LI-DNP Powered by JazzHR LihdAEAgf2

Job DescriptionCompany Description • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices., • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners. Job Description Responsibilities: • Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s)., • Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets., • Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements., • Provides input in the design and development of case report forms and clinical databases., • Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs., • Programs for quality checks for clinical study raw data and report the findings to Data Management., • Provides input in the design and development of case report forms and clinical study databases., • MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 5 years., • Experience in providing statistical programming support to early and late phase clinical trials., • Excellent skills in SAS programming and statistical reporting., • Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements., • Familiarity with FDA and ICH regulations and guidelines., • Excellent problem-solving skills., • Good written and verbal communication skills and organizational and documentation skills., • Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc., • Ability to prioritize and multi-task effectively., • Demonstrated positive attitude and the ability to work well with others.Additional Information All your information will be kept confidential according to EEO guidelines.

Job Description Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator in our New Jersey location. The ideal candidate will possess prior medical assistant or clinical trial experience, phlebotomy skills, fully bilingual in Spanish and English, and have a strong desire to work directly with diverse patients. Responsabilities, tasks, skills but not limited to: • Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc., • Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc., • Work with study participants on completion of study related visits, as well as follow-up and reminder phone calls., • Data entry of case report forms, and study visits across all study platforms within a maximum of 24hrs from the time data as collected., • Possess an acute attention to detail for clean data entry, regulatory compliance, site visits, study set-up and maintenance, and protocol adherence, • An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others, • Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies, • The position is responsible and accountable for recruitment directives, meeting financial goals, and the overall study operations. The study coordinator also significantly participates in the clinical trial coordination process., • Promoting the mission of ECRI to function as an Integrated Site Network providing unparalleled service to our clinical trial partners., • Meeting and exceeding priorities as discussed quarterly with direct supervisor., • Managing daily site operations., • Ensuring adherence to ECRI’s Standard Operating, • Ensuring the site’s compliance with all federal, local, and regulatory requirements and company procedures., • Work closely with pharma sponsor clinical research professionals in the processing and preparations for submitting regulatory documents., • Development of case report forms., • Other clinical research activities as assigned., • Bilingual English and Spanish, being able to recruit and consent a patient in both languages, • 4-year degree or equivalent preferably within Biology, Pharmacology, or a health-related field of study., • Ability to successfully adapt to a constantly changing environment., • Minimum of 1-2 years of experience in clinical research trials., • Must have superior interpersonal and communication skills with a strong customer service focus., • Completed the CITI training before start date., • Be friendly and engaging and demonstrate excellent organizational and time management skills., • Be able to conduct independent research activities., • Be extremely motivated and self-starter., • Be able to meet deadlines., • Participate in occasional health fair events, and community outreach activities on weekends., • This position does involve direct contact with patients and includes performing phlebotomy procedures, as needed. Occupational Health and Safety Risks include potential exposure to blood borne and airborne pathogens, thus candidate must ensure to always use universal precautions when handling biological samples, and supplies., • This position may involve occasional travel, including airplane travel, to attend ECRI Leadership Meetings and Investigator’s Meetings., • Taking ownership of their assigned studies and patients, • Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction, • Showing up on time, every time, • Competitive compensation, 401(k) with Company match, • A clear career pathway for advancement within the Company, • Health and Dental insurance Plans, • Generous PTO, • 9 Paid Federal Holidays, • Paid sick days Company DescriptionWho We Are ECRI is a clinical research institute with headquarters in Washington DC and sites in Chicago and New Jersey. ECRI has been recognized by Merck as their Diversity Center of Excellence as well as many other important pharma companies. The main focuses are on: Increasing patient access to research trials within our diverse communities (hispanic, black, asians) Providing physicians with enhanced care options for current patients, and Deliver superior clinical research enrollment metrics to Pharma sponsors All with the goal of Improving Patient Outcomes at the point of care. We want you to join us in doing just that.Who We Are\r\nECRI is a clinical research institute with headquarters in Washington DC and sites in Chicago and New Jersey. ECRI has been recognized by Merck as their Diversity Center of Excellence as well as many other important pharma companies. \r\nThe main focuses are on:\r\nIncreasing patient access to research trials within our diverse communities (hispanic, black, asians)\r\nProviding physicians with enhanced care options for current patients, and\r\nDeliver superior clinical research enrollment metrics to Pharma sponsors\r\nAll with the goal of Improving Patient Outcomes at the point of care.\r\nWe want you to join us in doing just that.

Job Description Overview: Vitalief is a trusted partner working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our team in Livingston, NJ. This position supports a groundbreaking study focused on predictive biometric markers for pre-eclampsia at one of the busiest perinatal clinics on the East Coast. The clinic, staffed by 11 doctors and managing around 6,500 births per year, sees approximately 600 potential patients monthly with a target enrollment of 100-200 participants. WHY VITALIEF? • You can actively contribute to our clients’ mission of advancing scientific discoveries that have the potential to change patients' lives for the better., • Our PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief employees., • We give everyone a seat at the table – we encourage innovation., • Life/work balance that includes 20 PTO (Paid Time Off) days plus 9 paid Holidays annually., • Other benefits include Company paid life insurance and short / long term disability coverage; 401K retirement program; Robust healthcare plans to choose from.Salary Range: up to $50,000 - based on experience level. Work Location & Hours: 100% on site in Livingston, NJ. 40 hours per week, approximately 7:30 AM – 4:00 PM (flexible start time) Responsibilities: • Work under the supervision of two Principal Investigators, collaborate effectively with team members and trial participants; coordinate and execute all aspects of a clinical research study focused on predictive biometric markers for pre-eclampsia., • Facilitate patient screening, consenting, and enrollment from a high-volume clinic., • Manage three key patient touch points: Conduct blood draws and administer a specialized blood pressure tool provided by the study during the first visit; re-administer blood pressure measurements, document clinical changes, and collect study data during the second visit; and repeat procedures as performed during the second visit in the final visit., • Accurately record and manage study data using the trial sponsor’s systems., • Maintain comprehensive research records in adherence to Good Clinical Practice (GCP) guidelines and study protocols., • Assist with the consent process and ensure timely communication with patients and research staff., • Act as a liaison between Principal Investigators, clinical staff, and patients to ensure timely delivery of study services., • Collaborate effectively with team members to facilitate smooth study operations.Required Skills:, • Bachelor’s Degree and Good Clinical Practice (GCP) certification., • Minimum of 1 year experience as a Clinical Research Coordinator., • Experience in patient recruiting/screening/consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and reported within reporting deadlines outlined in the protocol., • Proficient in performing blood draws (phlebotomy) and administering blood pressure measurements accurately., • Proficiency in Microsoft Office and familiarity with electronic health records or clinical trial management systems., • A compassionate, professional demeanor, ensuring a positive first impression and patient experience., • Exceptional communication skills to establish rapport with patients and team members., • Excellent time management and multitasking abilities in a fast-paced environment., • Strong organizational skills with meticulous attention to detail., • Ability to troubleshoot issues independently and escalate when necessary. 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. #LI-DNP Powered by JazzHR jG2992LsRl

Job Description NS Pharma is a highly focused, research-driven biopharmaceutical company working in rare diseases. We're exploring the potential of cutting-edge science as a subsidiary of Nippon Shinyaku Co., Ltd. In Japan. Job Summary: Responsible for the oversight and management of GMP Quality Assurance activities related to NS Pharma’s Quality systems, including the oversight of the supply chain for commercial and investigational products, the quality set up for the new products, the oversight of auditing, developing and executing system audit plans, providing regulatory guidance, coordinating inspection readiness activities, etc. under the direction of the GMP Quality Assurance Director. This is a hybrid position that requires to be in the Paramus office twice a week. Essential Duties and Responsibilities: • Supports ongoing development and operation of the quality function and GxP quality management system., • Supports the internal and external audit conduct to ensure patient safety and data quality., • Develop a new SOP and maintain the current SOPs for GMP., • Manage change control, deviation control, GxP training, validation, product recall and other GMP activities., • Release the products for commercial and clinical trials., • Prepare and review the quality agreement with the vendors/suppliers and licensees., • Prepare the response to the product complaints and product inquiries., • Oversee the vendors/suppliers such as 3PL and packager for GMP activities and serialization system., • Contributes to corporate quality-related goals and objectives., • Provides key process indicators to support management review., • Maintains a thorough knowledge of industry expectations and provides guidance and assistance to ensure NS Pharma sustains effective and efficient GxP systems., • Utilizes thorough knowledge of regulatory expectations to assess and effectively communicates compliance risks., • Performs audits of processes, departments and systems, internally and externally including documents against NS Pharma Standards and applicable regulatory requirements., • Coordinates FDA inspections by providing requested information and preparing NS Pharma and sites for inspections., • Prepares and reviews audit reports based on audit results., • Provides guidance and assistance in the development of corrective action commitments and performs regular follow-up., • Is a mentor to new or less experienced GMP staff., • Gives technical guidance and manages auditors in GxP training and preparation of audit reports., • Strong leader with the ability to identify potential problematic areas or situations and contributes to and/or collaborates on solutions that can be implemented in a timely fashion, managing priorities and with a commitment to quality and customer focus., • Thorough knowledge of applicable regulations from FDA and international agencies for commercial and investigational products., • Manages complex situations and is effective in influencing compliance decision-making., • In depth knowledge of GxP Audit processes., • Strong experience in GxP Quality Systems., • Experience with change control, deviation control, product complaint handling, validation and other GMP activities. Experience in Investigations, Root Cause Analysis, CAPA and Effectiveness check processes, tools, and techniques., • Experience with risk management principles and processes., • Well-developed communication skills (verbal and written), • Possesses a high level of maturity and character., • Possess the ability to speak in front of groups or training seminars., • B.S. or B.S./M.S. in Chemistry, Biology, or related fields. NS Pharma employees embrace our Mission to Help People Lead Healthier Happier Lives. We pride ourselves in offering employees and their families a robust Compensation and Benefits package designed to meet their needs, on and off the job. The annualized target salary range for this role is $135,000 to $150,000; actual salaries will vary and may be above or below this range depending on several factors, including experience, education, training, location, and merit. Other benefits include: • Medical, Dental & Vision Insurance, Basic and Voluntary Life and AD&D Insurance, Short- and Long-Term Disability Insurance, Flexible Spending Account, Health Savings Account, and Employee Assistance Programs, • Discretionary Bonus Programs and Long-term Incentive Plan, • Retirement Savings 401k with company match, • Generous Paid Time Off, Sick Time & Paid Holidays including a paid Year-End Shutdown., • Career Development, Progression and Training, • Flexible Work Arrangement Programs Applications will be accepted until August 8, 2025, or until a candidate is hired. Applicants not hired will remain in our Talent community for future opportunity consideration. Thank you for your interest in NS Pharma. NS Pharma is an EEO employer.

Job Description OB DESCRIPTION: • The GCP Quality Assurance Sr. Auditor will report to the Director the GCP/PVG Quality Assurance. This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Companys compliance directives and supporting quality management systems to ensure compliance and minimize risk in a regulated pharmaceutical environment. The incumbent will conduct and or participate in all GXP QA audit programs which include both internal and external GXP audits. This position will provide day to day support to the GXP QA Director in clinical operations/Non-clinical and Manufacturing to manage CROs, CMOs, investigator sites, and all relevant vendors to support clinical trials., • The Sr. Auditor of Quality Assurance will work with the QA and cross functional teams, communicate with QA consultants and has contact with external auditees, vendors, partners and affiliates. The ideal candidate will have extensive GCP experience., • Plan and conduct scheduled global clinical process and clinical vendor audits across all clinical trials., • Plan and conduct audits of specific clinical processes based on risk., • Perform clinical vendor audits along with various SMEs (IRT, EDC etc.) to comprehensively assess all services provided by a vendor., • Develop audit reports and distribute them to appropriate stakeholders., • Own and manage related clinical vendor non-conformances., • Review, understand, and audit clinical related regulations and guidelines (e.g. FDA regs, GCP, etc.)., • Collaborate with clinical sourcing, supplier quality and clinical partnership to manage clinical vendors., • Support the preparation, coordination, and participation of regulatory agency inspections., • Bachelors degree in a scientific, health care, or related discipline., • Minimum 5+ years of experience in the pharmaceutical industry, • The ideal candidate will have extensive GCP experience., • Proven experience conducting and managing internal and external GXP audits, including clinical development and safety/pharmacovigilance audits., • GCP guidelines and global regulatory requirements (e.g., FDA, EMA, ICH GCP)., • auditing CROs, CMOs, investigator sites, and clinical vendors., • clinical systems such as IRT and EDC from an audit perspective., • Prior experience in a biopharmaceutical company focused on neurology or psychiatry therapies.

Job DescriptionReceptionist/Recruiter Location: Secaucus, NJ Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Duties: Responsible for serving as the receptionist of the Clinical Research Center. In addition to working as the receptionist for the Frontage CRC, maintain an organized office environment in the day-to-day operation of the Frontage Clinical Research Center (CRC). Supervises: None Qualifications: High School Diploma, Associate’s preferred. Medical background is required. Experience: Minimum 3-5 years of experience working as receptionist for a large health care or research organization. Must have experience in analyzing and solving problems, communicate effectively, both verbally and in writing, created, composed and edited written materials, gathered data, compiled information, organized and establish priorities. Experience in taking notes, dictation and transcription. The ideal candidate will possess a minimum of 3-years progressively responsible experience with advanced computer skills in MS Word (type 50 WPM), extensive spreadsheet on Excel proposals, PowerPoint presentations, Internet searching capability and organization of e-Recruitment system. Also must have database management and records maintenance experience. Bilingual (English and Spanish) language skills desirable. Specific Responsibilities: Primary receptionist responsibilities for the Clinical Research Center. Assist and oversee visitors (including research subjects) with sign-in and sign-out procedures of the Clinical Research Center. Interact with study volunteers, sponsors and vendors and other clients. Forward all phone calls to appropriate department and staff. Maintain appointment calendar and make travel and lodging arrangements; compose and produce business correspondence, reports or directs related materials, and reviews and sign, as authorized. Edit documents; respond to inquiries and requests for information requiring knowledge of departmental and Frontage CRC policies and procedures. Prepare/distribute related materials, record minutes, and summarize for typing and distribution. The candidate will be responsible for assisting and actively participate in study subject screening and enrollment process. Strong interpersonal skills, flexibility, and the ability to function in a fast-paced environment as a team player are essential. Familiarity with the basic eligibility requirements and study procedures for specific study protocols and the process of a volunteer participating in a research study (e., ability to explain basic study eligibility requirements and procedures to a lay person). Recruiter for research subjects. Salary and Benefits: Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance. Salary: $18 - $22 per hour Benefits: • 401k Employer Match -Low PPO -High PPO -High PPO • Vision Insurance, • FSA (Medical, Dependent Care, and Commuter), • Short Term Disability, • Long Term Disability, • Life Insurance, • Generous PTO Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability. *

The VP of Global Clinical Operations is responsible for the management, oversight, and direction of the clinical operations function in the execution of all aspects of end-to-end clinical trials with the utmost compliance and quality consistent with Good Clinical Practice (GCP). Manage the Safety Al

Associate Director, Strategic Product Management (Life Sciences Products & Platform). Minimum 10+ years of complex solutioning experience, with broad life-sciences domain experience. Industry knowledge: Deep knowledge of Life Sciences and Clinical Trials ecosystem; ability to communicate across stak

Electro Mechanical,Instrument Maintenance,Adobe Dreamweaver,Document Control Management,E-Commerce.

Risk Management,Negiotiation,Operational management,Smartsheets,Strategic Planning,Team Management,Budgeting,Leadership Experience,Program Development,Supervising Experience,Financial Planning. They will lead all aspects of school operations including safety talent management and development adminis

Risk Management,Negiotiation,Operational management,Smartsheets,Strategic Planning,Team Management,Budgeting,Leadership Experience,Program Development,Supervising Experience,Financial Planning. This role combines strong business management skills with a clear understanding of programmatic goals ensu

Bachelor’s degree in Construction Management, Civil/Architectural Engineering, or related field preferred; equivalent industry experience considered. Demonstrated expertise in scheduling, procurement, budgeting, cost control, financial reporting, and client management. Proficiency with project man

Risk Management,Negiotiation,Operational management,Smartsheets,Strategic Planning,Team Management,Budgeting,Leadership Experience,Program Development,Supervising Experience,Financial Planning.

Works closely with in-house Project Management teams to actively manage client budgets and schedules.

Business Process,Risk Management,Key Stakeholders,Sigma,Financial Systems,Finance,Accounting,PMO,Project Management,ERP,Financial Project,Financial Statements,Ensure Compliance,Financial Management,Special projects.

Experience in project management, ideally within pharma, medical education, or a related field.

Risk Management,Negiotiation,Operational management,Smartsheets,Strategic Planning,Team Management,Budgeting,Leadership Experience,Program Development,Supervising Experience,Financial Planning.

Bachelor’s degree in Law, Operations Management, or related field (preferred). Prior experience in property management or real estate required. Experience with budgeting, financial reports, and project management.

Project Management Methodology,Project / Program Management,Construction Estimating,Construction Experience,PMBOK,Visio,Construction Management,Project Management,Project Management Software,Microsoft Project,Project Management Lifecycle,Contracts.

They must possess strong product management experience, excellent communication skills, and prior experience with data conversions and system transitions. Coordinate with stakeholders, ensuring smooth communication and expectation management. Knowledge of best practices in HR/Finance technology, com

Provide regular progress updates to management and stakeholders. Strong background in pricing jobs and proposal management. Abinitio,Cobol,Environmental Consultancy,Facility Management,Insulation,Asic.

The Sales Project Manager is an extension of the sales team, responsible for the continuous management of projects and revenue growth. Years of Project Management experience is a requirement.

Expertise with digital project management or field service software (e. Bachelor’s degree in Construction Management, Civil Engineering, Architecture, or related field preferred.

Risk Management: Create, monitor, and control risk management plans. Experience in Stakeholder management, requirement management. Change Management: Perform integrated Change Management Control.

Works closely with in-house Project Management teams to actively manage client budgets and schedules.

The SPM will be responsible to lead design teams and Construction Managers in both the pre-construction due diligence, design and scoping process with a focus on quality management, project controls, and user engagement as well as leading their teams through the bidding and construction administrati

Own the end-to-end management of the sales pipeline for vertical markets, ensuring data integrity, visibility, and actionable insights. Identify and implement process improvements across pipeline management, forecasting, reporting, and deal execution.

The SPM will be responsible to lead design teams and Construction Managers in both the pre-construction due diligence, design and scoping process with a focus on quality management, project controls, and user engagement as well as leading their teams through the bidding and construction administrati

Problem-solving, planning, and project management skills. This position is for a professional with deep knowledge and highly developed technical expertise in Project Management, who develops project plans and budgets.

Bachelor’s degree in Construction Management, Civil Engineering, or related field (preferred).

This role oversees critical infrastructure, ensures high service availability, and leads cross-functional communication with clinical and administrative teams. Standardize and continuously improve processes for endpoint management, ticketing workflows, and service delivery. Desktop/End-User Devices:

Join this 85yr+ general contractor that focuses on commercial projects in NYC.This firm has been operating in NYC for the past 85 years! They are a well-respected firm that has a ton of work right now.They focus on commercial and institutional clients/projects (think high-end office space or healthc

Strongly preferred Construction Engineering, Building Management, Construction Management, or equivalent degree. Be responsible for the administration, implementation, and management of projects and accountable for assigned scope of work, schedule and budget. Knowledge of construction management pro

Strong understanding of buyout, cost reporting, and change management.

This role will be primarily focused on managing implementation, coordination, and communication of an analytics driven project.Manages cross functional teams to deliver.

Lead project planning, including scope, schedule, budget, and resource management. Minimum 5 years of project management experience (mid–large scale projects). Excellent communication, organizational, and stakeholder management skills.

Bachelors or Masters degree in engineering, business, project management, or a related field. Excellent communication and stakeholder management skills.

A National General Contractor specializing in commercial projects, from full build outs and renovations to large scale projects is seeking a talented Assistant Project Manager to help assist with new and existing construction.This position is based out of their office in Union County, NJ.Benefits +

Location: 3 days office NJ Duration: 06 Months plus Rate: DOE USC & GC are Preferred.JD: Manage large to medium-scale or low to medium to high complexity projects within programs and standalone projects.Responsible for delivery of project.Lead stakeholders in the refinement of the project charter.De

Join this 85yr+ general contractor that focuses on commercial projects in NYC.This firm has been operating in NYC for the past 85 years! They are a well-respected firm that has a ton of work right now.They focus on commercial and institutional clients/projects (think high-end office space or healthc

Drive profitability through effective P&L management, budgeting, labor control, and food cost management.

Prepare and present regular project status reports to senior management and stakeholders.

SAP Project Manager with S4 and semiconductor experience.Deep understanding of the business process being automated by the SAP system.Good verbal and written communication.

Provide complete design and project management for all clients.

This position is for a professional with deep knowledge and highly developed technical expertise in Project Management, who develops project plans and budgets. Problem-solving, planning, and project management skills.

Senior NetSuite Lead Or Project Manager.Senior NetSuite lead or Project Manager with extensive experience working with NetSuite, Sage and Business Intelligence Tools (PowerBi/ or Domo/Data Lakes) Rochelle Park, NJ (Hybrid 3 Days in a week) Full Time Web Cam Interview We need a senior NetSuite lead o

Manage the scrum process by coordinating with the Scrum Team as well as with the other Scrum Masters and be flexible to participate in-person onsite scrum events (minimum 3 days per week).Be detailed, oriented and organized to keep the squad on track with deliverables at the same time be able to for

Engage in project management, multitasking, and client interaction. Participate in data management, proposal writing, and conferences. Your role will also include reviewing and interpreting data collected by our systems, writing perimeter air monitoring plans and proposals, and engaging in project m

Project Manager Medicaid / Medicare.Location: Penn Plaza East, Newark.Contact: W2 Location 3 Penn Plaza East, Newark- ONSITE DAY ONE - needs to be in office for 5 days in a month.Project managers with 10+ years of solid health care industry experience.

Updates job knowledge by tracking technology and project management advances; participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations.

The role partners with stakeholders across Commercial and the segments and within the client's Digital Technologies group to deliver new Commercial technology solutions.

Identify and implement process improvements across pipeline management, forecasting, reporting, and deal execution. Own the end-to-end management of the sales pipeline for vertical markets, ensuring data integrity, visibility, and actionable insights.

Strong time management, goals setting, and.

Updates job knowledge by tracking technology and project management advances; participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations.

Bachelor's degree in engineering, architecture, management, or related field. Must demonstrate strengths in technical knowledge, methods of operations of building maintenance and systems, leadership and supervisory skills, planning and assessment, human relations, budgeting and change management.

Updates job knowledge by tracking technology and project management advances; participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations.

The role partners with stakeholders across Commercial and the segments and within the client's Digital Technologies group to deliver new Commercial technology solutions.The candidate will lead one large or several small/medium projects globally.This role plays a vital role in the success of business

Updates job knowledge by tracking technology and project management advances; participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations.

Project Manager Medicaid / Medicare implementation experience (2 open roles) Client Client Horizon Location 3 Penn Plaza East, Newark - ONSITE DAY ONE - needs to be in office for 2-3 days in a week Duration- 10+ months extension up to 1 year Visa- any Project managers with 10+ years of solid Healt

Our client is a well-established general contracting and construction management firm based in Northern New Jersey, with over two decades of experience delivering complex public construction projects. Manage all phases of project lifecycle including bidding, scheduling, budgeting, subcontractor mana

Responsible for defining, enforcing and promoting policies and programs to ensure best in class customer experience and hence drive customer satisfaction across our market.

Construction Project Management. Degree in Engineering, Architecture, or Construction Management. Excellent communication skills with various parties including management, subcontractors, consultants, architects, vendors, and clients.

Infrastructure Project Manager.Location: Newark, NJ Type: Contract-to-hire.Ideal background: It would be best to have infrastructure experience.If possible, merger and integration would be a big plus.They should be a technical pm networking, servers, db's all good knowledge areas to have.They have

Establishes work plan and staffing for each phase of the project, works closely with Project Executive and HR team to manage the relationship with staff and craft Form and lead an effective project management team, define and delegate management responsibilities, and set goals Review and control o

Bachelors or masters degree from an accredited college or university, or eight (8) years progressive experience in multi-unit foodservice, hospitality management, plant operations management, environmental services, laundry distribution or other Support Services areas in lieu of degree. Champions de

Proven experience in project management and team leadership. Our teams partner with public- and private-sector clients to create innovative, sustainable and resilient solutions throughout the project lifecycle from advisory, planning, design and engineering to program and construction management.

Assistant Director Of Human Resources Operations.Reporting to the Director of Human Resources Operations, the Assistant Director of HR Operations plays a pivotal role in ensuring the smooth and efficient functioning of the University's human resources processes.This position leads a range of operati

Oracle Fusion Cloud Techno Functional Practitioner.Required: Oracle Fusion Cloud Techno Functional Practitioner with minimum 10 years experience with managing large Oracle Fusion Cloud programs especially in the Banking & Financial Services Domain.Understanding of data flow right from initiation to

Develop proficiency in project documentation, reporting, and technology tools used in restoration management. Participate in structured training and mentorship programs designed to build skills in project management, leadership, and technical expertise. Strong organizational and project management s

Strong understanding of buyout, cost reporting, and change management.

Participate in structured training and mentorship programs designed to build skills in project management, leadership, and technical expertise. Strong organizational and project management skills. Develop proficiency in project documentation, reporting, and technology tools used in restoration manag

Join this 85yr+ general contractor that focuses on commercial projects in NYC.This firm has been operating in NYC for the past 85 years! They are a well-respected firm that has a ton of work right now.They focus on commercial and institutional clients/projects (think high-end office space or healthc

Presents to management and/or customers on project updates, project cycle, and expected results. Expectation that Project Management Professional certification will be obtained within two years of employment in the position.

Excellent communication and stakeholder management skills. They must possess strong product management experience, excellent communication skills, and prior experience with data conversions and system transitions. Coordinate with stakeholders, ensuring smooth communication and expectation management

Proficient in project management/construction management software. Construction Project Management. Degree in Construction Management or related field strongly preferred.

The Sales Project Manager is an extension of the sales team, responsible for the continuous management of projects and revenue growth. Years of Project Management experience is a requirement.

Bachelor's Degree in Construction Management (strongly preferred). Knowledge of project management software.

A National General Contractor specializing in commercial projects, from full build outs and renovations to large scale projects is seeking a talented Assistant Project Manager to help assist with new and existing construction.This position is based out of their office in Union County, NJ.Benefits +

A successful Assistant Project Manager should have: a background in construction or a related field within the property industry; strong organizational and time management skills; effective communication and collaboration abilities; proficiency with project management tools and software; an ability

Lead project planning, including scope, schedule, budget, and resource management. Minimum 5 years of project management experience (mid–large scale projects). Excellent communication, organizational, and stakeholder management skills.

Construction Project Management. Degree in Engineering, Architecture or Construction Management. Excellent communication skills with various parties including management, subcontractors, consultants, architects, vendors, and clients.

Experience in project management, ideally within pharma, medical education, or a related field.

Open and transparent communication with senior leadership as well as local office management.

Bachelor’s degree in Construction Management, Civil Engineering, Architecture, or related field preferred. Expertise with digital project management or field service software (e.

Proven experience in project management within the construction industry.

Prepare and present regular project status reports to senior management and stakeholders.

General knowledge of project management and construction management administration. Strong project management skills (e. Financial analysis skill, including budget management, business modeling, and basic accounting knowledge.

Bachelor’s degree in Construction Management, Civil/Architectural Engineering, or related field preferred; equivalent industry experience considered. Demonstrated expertise in scheduling, procurement, budgeting, cost control, financial reporting, and client management. Proficiency with project man

The ideal candidate must have a Bachelor's degree in Construction Management, Architecture, Mechanical, Electrical Engineering or related field. Formal training in project management is preferred.

Collaboration with project teams, construction sites, and management is essential to ensure successful project execution. Join our team and be a part of shaping the future of facility management and construction excellence. Communicates all project issues to the appropriate level of management in a

Client management and overall satisfaction.

Collaboration with project teams, construction sites, and management is essential to ensure successful project execution. Join our team and be a part of shaping the future of facility management and construction excellence. Communicates all project issues to the appropriate level of management in a

Presents to management and/or customers on project updates, project cycle, and expected results. Expectation that Project Management Professional certification will be obtained within two years of employment in the position.

Required Skills: The ideal candidate must have a Bachelor's degree in Construction Management, Architecture, Mechanical, Electrical Engineering or related field. Formal training in project management is preferred.

Are you the type of person who thrives on organization, follow-through, and keeping all the moving parts in sync? Do you enjoy supporting a team, owning daily operations, and playing a key role in bringing beautiful spaces to life?.We're Kitchen & Bath Tune-Up of Bloomfield, NJ a fast-growing, fami

Our people are Stantec's most valuable resource, and in joining our team you will be able to leverage your career experiences and expertise in project management and business development and contribute to the growth of the structural group and Stantec. Demonstrated skill at project management/busine

Project Management & Leadership. Organizational and time-management skills, with the ability to prioritize tasks. Knowledge of project management software and tools, with the ability to develop and maintain comprehensive project plans and documentation.

Bachelor's Degree in Construction Management, Civil Engineering, or related field.

A strong background in traffic engineering, project management, and prior supervision of professional staff. Substantial technical project experience and project management experience.

Responsible for the interior design, space planning, construction management, maintenance and operations of all company facilities and grounds, leased and owned. Responsible to maintain and utilize a facilities maintenance management and work order system. Senior professional with strong knowledge o

Our teams partner with public- and private-sector clients to create innovative, sustainable and resilient solutions throughout the project lifecycle from advisory, planning, design and engineering to program and construction management. The New York Metro Buildings + Places Team is a multi-discipli

You will be responsible for the day-to-day management of assigned projects, working closely with senior project managers or partners. Oversee the day-to-day management of assigned projects.

Bachelor's degree in civil engineering or construction management. Lead the design management of stations, bridge structures, and roadway elements, ensuring compliance with contract documents, AASHTO, and NJDOT standards. Support the Construction Management Division during construction to ensure tha

The ideal candidate must have a Bachelor's degree in Construction Management, Architecture, Mechanical, Electrical Engineering or related field. Formal training in project management is preferred.

Job is two days on site in Newark, NJ or msg.Looking for strong construction background with 10 plus years experience.Needs two references with submit that will be called by the client.

Work Location: HYBRID - Newark, NJ.Lead and oversee digital transformation initiatives related to Oracle Fusion Cloud within the organization.

Experience with project management tools to support initiative tracking.