icon Mechanical jobs in Stamford, CT - 90 jobs

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Inventory Coordinator- Farmingdale NY- onsite We are currently seeking an Inventory Coordinator to join our diverse and dynamic team. As an Inventory Coordinator at ICON, you will play a vital role in managing and optimizing inventory levels to ensure the availability of essential materials and supplies for clinical operations. You will collaborate with various departments to maintain accurate inventory records and support efficient supply chain processes. The Role: * Collect all deliveries from loading bay, log, QC, receipt in, store and distribute as required. * Maintain stock on shelves in a tidy manner, executing stock rotation in appropriate date order. * Record all stock movements and stock issues using Inventory control system. * Ensure accurate data entry. * Operate all Inventory Control systems (e.g., IDBS, ASID, and Excel) and other appropriate systems to facilitate stock processing duties. * Participate in stock cycle-counts. * Liaise with internal customers, suppliers, and the Purchasing and Finance departments on all stock related issues. * Perform any other duties as assigned by management * Follow department SOPs. * Other duties as assigned. To be successful, you will need: * High School or Equivalent (Required) * 1 to 3 years of experience * Must be able to lift up to 50lbs, utilize a pallet jack pushing and pulling pallets over 100Lbs. * Matching boxes to purchase orders * Assisting couriers removing incoming shipments from trucks. Hourly Rate $22.50 hour This is an hourly paid position, disregard the compensation section below. #LI-FL1 What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Salary range: $38,728.00-$48,410.00 Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Are you a current ICON Employee? Please click here to apply

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. Job Description Title: Safety Associate Location: Montvale, NJ Duration: 6+ (Possibility of Extension) PROFESSIONAL QUALIFICATIONS / EXPERIENCE • Experience in an environment of regulatory toxicology and product safety preferred. • Demonstrated experience in preparing product risk assessments, and developing risk mitigation practices, for chemical substances and preparations. • Competent at reviewing toxicology and related chemical safety data. • Working knowledge of mammalian toxicology assays and testing protocols. • Working knowledge of chemical legislation, safety and labelling of chemicals and preparations. • Demonstrated ability to handle competing priorities effectively. • Sound performer in interacting with, and influencing regulatory authorities and political lobbies. • Proven track record in active collaboration with R&D and non-R&D functions as well as third parties. • Pro-active self-direction with a high level of initiative and persistence and a very much hands on approach to results delivery. • The ability to effectively manage projects and relationships with local partners, contractors, and consultants to achieve CLIENT objectives. • Industry experience, preferably in FMCG; commercial understanding of corporate and operational business issues. Qualifications PROFESSIONAL QUALIFICATIONS / EXPERIENCE • Experience in an environment of regulatory toxicology and product safety preferred. • Demonstrated experience in preparing product risk assessments, and developing risk mitigation practices, for chemical substances and preparations. • Competent at reviewing toxicology and related chemical safety data. • Working knowledge of mammalian toxicology assays and testing protocols. • Working knowledge of chemical legislation, safety and labelling of chemicals and preparations. • Demonstrated ability to handle competing priorities effectively. • Sound performer in interacting with, and influencing regulatory authorities and political lobbies. • Proven track record in active collaboration with R&D and non-R&D functions as well as third parties. • Pro-active self-direction with a high level of initiative and persistence and a very much hands on approach to results delivery. • The ability to effectively manage projects and relationships with local partners, contractors, and consultants to achieve CLIENT objectives. • Industry experience, preferably in FMCG; commercial understanding of corporate and operational business issues. Additional Information Kind Regards, Indu Dubey Clinical Recruiter DIRECT # - (732)-844-8725 Email ID: indu @irionline.com

A Few Words About Us - Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Support the SAP/HR (PD) Module for all Enterprise Employees. Support the maintenance of all organizational structure (PD infotype) changes and ensure accuracy and integrity of the data. *Coordinate the updating of the SAP/HR module due to organization restructuring. *Perform mass updates utilizing the Mercury tool. *Perform root cause analysis and problem resolution for the SAP/HR module. *SAP Module Associate is responsible for testing new and enhanced SAP/HR (PA/PD) functionality in support of PSEG Long Island Clients. *Coordinate all activities that impact employee information with other SAP Modules and downstream applications. *Assist with SAP/HR training. *Incumbent must pay attention to detail, be results oriented, have the ability to identify and solve business problems. *Must be customer focused with strong written and verbal communication/presentation skills. *Responsible for reviewing and/or auditing payroll/HR master data. *Broad knowledge and understanding of the HR/SAP module. *High proficiency with MS Excel (including Pivot Tables) and MS Access. *Experience with Org Chart creation software. Qualifications Looking for someone who can hit the ground running. Minimum of a High school diploma 3-5 years of related experience MUST have SAP OM (organizational management) experience as well as Personnel Administration experience. Need to understand how making changes impacts other areas in SAP MS Excel experience - V-lookup would be a plus Will be located in Uniondale, NY. Not looking for individuals who would like to work remotely. Must be customer oriented Additional Information Regards, Nagesh Sr.Technical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I Direct# 732-429-1641 (BOARD) # 732-549-2030 - Ext - 305 LinkedIn: https://www.linkedin.com/in/nageshghanti Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

IRI believes in commitment, integrity and strategic workforce solutions. Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity. Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success. Job Description • Candidate will perform bio-functional assays in support of vaccine development • The incumbent will perform biological assays, including but not limited to neutralization assays & ELISAs • To monitor the immune responses elicited by various vaccine candidate s in support of pre-clinical studies & clinical trials • Incumbent will carry out specific laboratory experiments specific to the monitoring of humoral and/or cellular immune responses to various candidate vaccine antigens. • Analyze immune responses to vaccine candidates using techniques that include (but not limited to) various tissue culture techniques, ELISA, & neutralization assays. • Interpret & summarize experimental data. • Generate, characterize, & qualify reagents used to perform necessary assays & supports maintenance of laboratory supplies. • Satisfactorily completes all cGMP/GLP & safety training in conformance with department requirements. • Where applicable performs job responsibilities in compliance with cGMP/GLP & other regulatory agency requirements. • Present experimental results at group meetings, Maintain Laboratory notebooks in compliance with the client Laboratory Notebook Policy. Qualifications • BS/MS in any science related field with 1-3 years of related experience • ELISA experience preferred • Knowledge of cGMP/GLP • Knowledge of assay development Additional Information Regards Ricky 732-49-1925

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Title: Construction Supervisor Location: 175 E. Old Country Rd, Hicksville, NY Duration: (Part time contract position) Direct client: Immediate interview “ON CALL” contractors - meaning they will be needed from time to time, during peak work. Anywhere from 100 to 300 hours a year. Oversight of all contractor activities on major contracts throughout Long Island. Ensure contractors are following specifications and drawings. Following OSHA guidelines. Will be record keeping, coordinating and evaluating % complete. Will be acting as onsite representative. Occasionally dealing with customers. 95% of work is transmission, substation expansion, new substations, and high voltage. ***NO direct contact. However, the contractors under their supervision will be in close proximity of energized high-voltage equipment and bus inside the substations so they must be aware of safe working distances as outlined by OSHA. ****Candidates must drive their own vehicle - only employees are permitted to drive company vehicles. I will consider mileage reimbursement for significant travel from their home to remote locations. • May be needed 2-3 weeks at a time, possibly a month • Need individuals who can come on with a weeks' notice Job Description: • Direct, coordinate, inspect, monitor and document the performance of outside contractors performing construction and maintenance on LIPA facilities. • Serve as principle on-site interface between contractors and various Client's operating and engineering departments, customers, municipalities and regulatory agencies. • Assure project meets technical specifications and is completed within cost and schedule requirements by enforcing all of the contract's terms and conditions. Responsibilities (include and are not limited to): • Monitor project progress and contractor performance through field inspections covering quantity and quality of work performance • Write procedures which will be submitted for line and equipment clearances on distribution facilities. • Take and return clearances when required for each assigned project. • Assist in direction and evaluation of inspections and testing of materials, equipment and systems. • Maintain accurate records of site conditions, work performed and potential scope changes. • Determine value of work complete and assist Work Coordinator in review and approval of contractor invoices. • Identify and initiate corrective action to resolve issues with engineering/design, materials, procurement, construction, interdisciplinary/interdepartmental coordination, worker productivity, safety and quality items. Decisions must be made and implemented within parameters established with minimum delay. • Participate in constructability reviews with engineering and operating areas to offer cost saving suggestions during the project design phase. • Review and comment on bid strategy, specifications and drawings. Recommend engineering & design changes. • Assist with preparation of project cost estimates, detailed construction and payment schedules. • Assist the Work Coordinator as required in the development and implementation of the regional work plan. • Coordinate engineering, material and permit requirements as required. • Monitor and report on any incidents, potential hazards and/or environmental concerns in order to ensure area work complies with SHE policies/regulatory requirements. • Manage the day to day relationship with customers/business areas in order to understand their requirements and deliver appropriate solutions, in line with Client's policies and programs. • Develop and maintain effective relationships with customers to promote a positive image for both Clients. Promptly resolve customer concerns. • Ensure compliance with all Corporate Safety policies and procedures and OSHA rules and regulations. Required Skills, Knowledge and Experience: • Bachelor's Degree in Engineering, Construction Management or related technical field and minimum three (3) years direct related experience. Candidates without a degree with significant construction experience (minimum eight (8) years) will be considered. Key characteristics & accountabilities for the successful individual are as follows: • Ability to monitor the progress and performance of multiple projects being worked simultaneously. • Detailed working knowledge of electric substations, electric transmission and distribution systems, civil construction and lead/asbestos abatement experience • Knowledge of electric system operations and procedures for submitting for line and equipment clearances on transmission and distribution facilities. • Knowledge of specification and contract enforcement, applicable technical standards, OSHA and other regulatory statutes. • Knowledge of trade agreements, procedures, techniques, work methods and standards used in the construction industry. • Ability to read and interpret specifications and drawings and convey interpretations to contractors. • Ability to investigate and solve construction problems in a timely manner with minimum dependence on others. • Administrative skills for effective monitoring of contractor progress, cost control and contractual interpretation matters. • Possess excellent communication skills to deal effectively with all contacts - professional and craft. Job Dimensions: • Reports to: Projects & Construction/Project Management Work Coordinator • Employees: Responsible for the oversight of 2-35 contractor employees. • Budget: Oversight of contracted capital projects valued at $25,000- $5,000,000 • Claims Negotiations: $1000- $1,000,000 • Number of projects assigned on an concurrent basis: 3-6 • Work assignments cover all client's service territories from Far Rockaway to Eastern Long Island Experience Requirements: • 3 to 5 years' experience with a 4 year degree OR 7 to 10 years of experience with no Degree • Experience in fact finding including knowledge and understanding of where to find and how to present relevant information. • Experience of using project/contract management systems in order to understand and analyze data. Experience is often acquired through on the job training. • Proficient in relevant software e.g. Microsoft Office products (Excel, Word, Project) • Knowledge of client's business operations, company policies and practices. • Operating experience working with SAP Additional Requirements: • Valid Driver's License • Personal Vehicle Additional Information Thanks, Nagesh 732-429-1641

The Associate Director - Medical Writing will be the designated Lead Medical Writer for approximately 3 Neuroscience or General Medicine Programs, responsible for providing needed support and direction to other staff/contractors on these programs. As the lead writer, the incumbent ensures timely completion, accuracy and quality of all clinical and submission documentation across all aspects of the compounds' life cycle management. Due to the complexity of the programs, the incumbent must rapidly acquire complete and advanced knowledge of the compound to ensure alignment and consistency across studies. The qualified candidate will have proven ability to effectively manage the outsourcing of document preparation when necessary and the associated service providers. Responsibilities include but are not limited to: Working on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors Independently prepares and at times may direct, the writing of PCSs, protocols and protocol amendments Independently prepares and at times may direct, all the writing of the CSRs including narratives Works across functional areas to obtain all applicable source materials Leads the preparation of clinical sections of submission documents, such as the briefing books, Global Investigator Brochures, and annual regulatory reports Leads the medical writing activities for marketing application submission documents Liaises with other functional areas and groups in the development of document standards and structure Interacts routinely with clinical research and biostatistics staff to gain comprehensive understanding of the study design, and results across the program Implements document quality controls, standards and best practices Qualifications Job Qualifications BS required/MS preferred Minimum of 8 years medical writing experience in an industry setting, with specific experience with compounds in Neuroscience Must have participated in or lead a major marketing application submission Strong critical thinking and problem solving skills Self-motivated with the ability to influence others Ability to multitask on complex projects Result driven with a mastery of time management and project planning Able to work on site Advanced working knowledge of MS project and MS Word Experienced in the use of a documentum system Additional Information All your information will be kept confidential according to EEO guidelines.

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Client: Direct Client Location: Woodcliff Lake, NJ Job Title: Senior Biostatistician Duration: 12 Months to 36 (Possible Extension) Summary: • Work closely with clinicians, programmers, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review. • Work with the clinical study team on study design, development and/or review of clinical study protocols. • Develop and/or review statistical analysis plans, including Table/listing/figure shells, and final study report for clinical studies; perform post-hoc statistical analyses as needed. • Work with the project statistician and clinical data managers on design/review of case report form, data transfer specification, edit check specification, and participation in user acceptance testing (UAT); generate/review data tables/listings and coordinate data review meetings during the course of the study to ensure data quality. • Oversee CRO programming activities, perform quality assurance checks on internally or externally produced SAS tables, listings, and figures, and ensure the quality of CRO deliverables. • May work with the Health Outcome team on the design/analysis/validation of projects. • May work on submission teams as a statistician and/or a programmer. • Act as lead Statistician on complex trials and across multiple studies. • Act as a lead representative of the of the biostatistics department on project teams. Feel free to forward my email to your friends/colleagues who might be available Qualifications Education & Experience: • Must have a MS in Biostatistics/Statistics with at least 10-12 years of experience or a PhD in Biostatistics/ Statistics with at least 6 years of experience in the pharmaceutical, CRO or biotech industry. • Strong SAS programming skills. - At least 3-5 years. • Oncology experience is highly preferred. • Good technical writing skills. • Good communication skills (verbal and written). • Strong teamwork ability/commitment and individual initiative. • Strong organizational skills with ability to effectively manage multiple projects. • We need is an experienced statistician who can do SAS programming at the same time can clearly interpret statistical concept and results to non-statisticians and key medical opinion leaders Additional Information Warm Regards, Jay Kaushik Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I (Direct) 732-429-1633 | (W) 732-549-2030 x 211 | (F) 732-549-5549 Linkedin: https://www.linkedin.com/in/jay-kaushik-a992a6a9?trk=hp-identity-name Visit to our Website: www.irionline.com Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

IRI believes in commitment, Integrity and strategic workforce solutions. Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity. Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success. Job Description • We are looking for a highly performing, self-motivated, detail oriented Scientist to support antibody drug conjugate (ADC) and targeted immunotherapy drug discovery at Oncology (ORU) in Pearl River, NY • The successful candidate will work in a matrixed team environment as part of the Oncology Rinat Research & Development (ORRD) Histology & Biomarker (OHB) group • The candidate will work as part of a team that uses histology and immunohistochemistry (IHC) methods to study protein/target expression, biomarker development, pharmacodynamics, efficacy and safety effects of molecules/compounds in development • The successful candidate will be responsible for overseeing the smooth functioning of the daily technical processes of the lab. Responsibilities- • Receive (physically and electronically) & QC the incoming pipeline of samples • Trimming, process and embed all blocks that come into the lab • Section and H&E stain samples for several lab initiatives, as independent projects to work on with hiring manager • Perform routine IHC of established panels of markers for several initiatives • Subsequently, work with the hiring manager and lab scientists to interpret the data and report to the relevant teams • Section blocks, coverslip slides and perform other supportive tasks for the program scientists in the lab • Order, receive and organize lab supplies • Maintain lab equipment (call vendors for service etc.) • Act as a liaison for the In Vivo Pharmacology group • Enter experimental data into the lab databases • Work with student workers to organize and inventory blocks Qualifications • The candidate must have worked in the research setting for minimum 3-5 years and prior histology experience is required • Additionally, the successful candidate will have cell biology training and a deep understanding of the scientific method • The candidate will be flexible and be able to adapt to change as the lab is in a dynamic research environment, responding to the needs of the ORRD research unit • We are looking for someone enthusiastic, energetic, able to follow instructions, detail oriented, agile to change, and will be an excellent and honest communicator • The successful candidate will be expected to maintain an electronic laboratory notebook, use email, and meet weekly with the group manager - therefore basic computer skills are required such as Microsoft Outlook and Office (Excel, PowerPoint) • Bachelors or Master's degree in biological sciences Additional Information Thanks Regards Ricky

Sample Management Coordinator - Full Time - Benefits - Farmingdale, New York (NY) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Sample Management Coordinator I to join our diverse and dynamic team. As a Sample Management Coordinator I at ICON, you will be responsible for the proper handling, tracking, and documentation of clinical trial samples. Your work will play a crucial role in ensuring the accurate and timely management of biological samples, contributing to the success of clinical research studies. What You Will Be Doing: * Coordinating the receipt, tracking, and storage of clinical trial samples in compliance with protocols and regulatory requirements. * Maintaining accurate documentation of sample collection, storage conditions, and chain of custody records. * Ensuring proper labeling and inventory of biological samples, and supporting the timely distribution of samples to laboratories for analysis. * Collaborating with clinical teams, laboratory personnel, and logistics providers to ensure timely and efficient sample management. * Assisting with sample-related queries and resolving discrepancies in sample tracking or documentation. * Contributing to process improvement initiatives in sample management and ensuring compliance with quality standards. Your Profile: * Bachelor's degree in life sciences, laboratory science, or a related field. * Experience in sample handling, logistics, or laboratory coordination, preferably within clinical trials or healthcare. * Strong attention to detail and organizational skills, with the ability to manage multiple sample management tasks simultaneously. * Excellent communication and teamwork skills, with the ability to collaborate with cross-functional teams. * Familiarity with sample tracking systems, laboratory protocols, and regulatory guidelines is an advantage. Compensation: Salary: $ 22 hour * This is for the Farmingdale location only . Disregard compensation further below. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Salary range: $38,728.00-$48,410.00 Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Are you a current ICON Employee? Please click here to apply

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Position: Data Analyst/Finance Analyst Location: 333 Earle Ovington Blvd, Uniondale, NY Duration: 3- Months Possible go perm Please note: It will be 50 Hrs work week initially 1- 2 weeks Job Description: • This position will be the primary supporting in the governance and oversight of the identification, development and use of technology in the balanced scorecard and benchmarking process. • The position specifically supports the governance of the Access databases, Excel spreadsheets, Tableau Software and back-up systems associated with the and Line of Business balanced scorecard process inclusive of related initiatives, analytics, benchmarking and diagnostics process. • Supports the implementation of new techniques, technologies and process improvement tools to assure quality adherence and process excellence. Completes assigned quarterly, monthly and weekly reporting requirements and supports the monthly and quarterly quality review process. • Gathers and links data from diverse sources and analyses to identify metrics, drivers, correlations, performance gaps and opportunities for improvement. • Supports the benchmarking efforts, target setting and goal development process inclusive of MICP, PIP, scorecard, Division and District level targets and goals. • Interacts with process owners and management to support and obtain feedback on all elements of the balanced scorecard and benchmarking process. • Maintains and applies working knowledge of Standards for Business Controls and meet management's expectations for effective internal business controls. • Required: BA or BS Degree preferably in Math/Econ, Engineering, Computer Science or Finance or equivalent experience. • Demonstrated organization and high level of analytical and quantitative skills. Experienced in database development or programming. • Must have extensive proven expertise in Excel and Access. Excel and Access skills will be tested as part of the interview process. • Demonstrated ability to develop new approaches with applicable tools to measure success. Demonstrated detail orientation and ability to work independently. Demonstrated ability to work across department boundaries. Desired: Masters/MBA or in progress. Working knowledge of SAP, DWMS, CMMS, OMS Additional Information Warm Regards Nagesh 732-429-1641

Manager, Scientific Affairs- Farmingdale NY - Hybrid ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Manager, Scientific Affairs- Farmingdale NY Hybrid The Manager, Scientific Affairs, acts as a scientific and technical liaison between business development and laboratory operations. The Manager, Scientific Affairs plays a role in establishing and maintaining partnerships with biopharma drug development translational and clinical biomarker teams. As such, this individual will participate in customer facing meetings to provide technical, regulatory and scientific consultation and will ascertain customer needs for assay development, assay validation, and clinical trial testing. The individual will review new clinical trial protocols and RFPs and provide technical input to the ICL/ISL Proposals teams. The individual will play a key role in developing a strategic roadmap for the evaluation and implementation of new testing platforms and capabilities in our global laboratory network. The individual may also provide technical and scientific support for marketing collateral and other activities. Job Description * Recognize, exemplify and adhere to ICON's values which center around our commitment to People Clients and Performance. * *Provide scientific support for client-oriented business development and related contractual activities as a subject matter expert on related technologies and methods for oncology biomarker analysis and clinical diagnostics * Review proposals, protocols and new and updated study specification documents for the tests that are required. Request clarification of requested tests when necessary * Review of new quotes, technical information, etc. for any new tests being tested at ICON Labs or referred to a reference lab. * *Act as a technical writer and editor for marketing collateral related to laboratory services * Evaluate diagnostic and biomarker assay market trends and opportunities across key therapeutic areas for strategic roadmap planning purposes * *Perform competitor analysis; provide updates on services offered by commercial laboratories who operate in the CRO industry * *Act as liaison between internal business development and assay development teams and laboratory operations on a project specific basis * Participate in company presentations to clients * Evaluate potential strategic partners and markets with respect to platforms, chemistries, biomarkers and applications for strategic roadmap planning purposes * Represent ICON at industry and scientific conferences * Maintain knowledge of related industry news and trends * Identify new opportunities to provide central and specialty lab testing services for new and existing biopharma customers * Complete assay development checklists and/or assay requirement checklist for custom assay development and validation opportunities * Other duties as assigned What you need: Advanced degree (MD, PhD, PharmD, or equivalent) in a scientific or healthcare-related field. Minimum of 6 years of experience. Protocol and clinical laboratory experience. #LI-FL1 What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Salary range: $121,576.00-$151,970.00 Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Are you a current ICON Employee? Please click here to apply

· Performs daily activities for 5 bi-weekly and semi-monthly payrolls to ensure accurate and timely compensation to employees for work performed. · Performs a variety of statistical tasks and clerical duties required to prepare payroll data for computer input. Reviews timekeeping records. · Processes exception items requiring special handling. Responds to inquiries from employees regarding deductions, calculations, and changes in compensation. · Prepares, compiles and maintains various statistical and payroll records. May perform analyses and reviews of data, develop reports for supervision review. Essential Functions · Performs payroll activities for bi-weekly and semi-monthly payroll processing. · Reviews timekeeping records for accuracy and completeness. · Process special payroll exceptions as needed. · W-2 processing knowledge desirable · Prepare payroll journal entries for posting to the general ledger. · Maintain master control file. · Knowledge of ADP and Peoplesoft Qualifications Bachelors plus Additional Information All your information will be kept confidential according to EEO guidelines.

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description • One year position for scientist in the cancer in vivo pharmacology group with in vivo experience in small mammals (mouse/rats-preference in immune compromised strains) to support a team of in vivo pharmacologists execute in vivo tumour biology studies both within the vivarium and research lab • The candidate must function as an integral member of the in vivo biology team, responsible for supporting all assigned aspects of in vivo testing in a coordinated manner with other members of the team • The candidate must be dependable and possess excellent time management, communication, and organizational skills. Qualifications • Mouse handling (preferable immune deficient), dependability, teamwork, sterile technique, tissue culture, and lab maintenance. • BS/MS in science related discipline **MUST BE MEDICALLY CLEARED FOR RESPIRATOR USE AND FIT TEST REQUIRED** Will be using a N-95 respirator. **CANDIDATE WILL ALSO HAVE TO BE OFFERED Hepatitis B Vaccine** Additional Information Thanks Warm Regards Ricky Bansal 732-429-1925

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. Job Description Job Summary Contribute to, review and approve imaging core lab documents: Data Transfer Specifications Communication Plans Imaging Core Lab RFPs and proposals Imaging Core Lab forms and study-related documents Review and design tumor assessment Case Report Forms in eCRF Review data derived from imaging aspects of protocols, collaborating with Clinical Operations, Biostatistics and Data Management Review tumor assessment sections of Patient Profiles from site CRF data and provide feedback to Data Management for site queries Act as the Imaging representative on teleconferences with CROs and imaging core labs Assess, analyze and proactively develop corrective action plans when needed Manage ongoing tumor assessment scan reconciliation between eCRF and Imaging Core Lab to ensure that all scans are received in a timely manner Description of Required Skill Set: Scientific background with understanding of clinical development and drug development process together with a broad understanding and experience of clinical operations or data management with clinical trials using medical imaging. Strong verbal, written and interpersonal communication skills, especially relationship management, with ability to give/receive feedback and build consensus Experience with managing the imaging aspects of clinical trials or studies and programs from protocol development to final analysis and submission. Experience in oversight and management of imaging CROs, to ensure successful conduct of the imaging aspects of clinical trials ensuring data integrity and quality. Familiarity with oncology image-based tumor response criteria (e.g. RECIST 1.1, mRECIST for HCC, ir RECIST) Ability to work semi-autonomously with strong organizational, prioritization and analytical skills Qualifications Qualifications Bachelor's degree required in associated scientific discipline, Imaging Technologist experience preferred; Master's degree strongly preferred 3+ years of pharmaceutical experience, with 3 years of experience with clinical trials with imaging aspects desired ONCOLOGY REQUIRED Must haves: Clinical Trial Imaging experience PHARMA or CRO (Pharma) Imaging on clinical trials Oncology Required RECIST experience Familiar with review of patient profiles to review tumor assessment data Additional Information Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus. Thank you. Kind Regards, Harris Kaushik Clinical Recruiter Integrated Resources , Inc. IT Life Sciences Allied Healthcare CRO DIRECT # - (650)-399-0891 Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Kit QC Inspector- Farmingdale, NY on site ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Job Advert Posting At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. Kit QC Inspector- Farmingdale, NY onsite The role: To ensure the quality and correctness of all visit kits distributed to investigator sites. Inspect all visit kits according to SOP prior to packing and transfer to the shipping department. Perform quality control of all visit kits as required by the SOP. Ensure all errors are corrected & logged appropriately. Inform the QC supervisor of any issues or delays. Achieve daily/weekly departmental Quota assigned. Perform additional responsibilities as requested by Management To be successful you will need: 2 to 3 years of QC experience Skills - Detail oriented, excellent organizational skills, Commutations skills and the ability to deal well with stress. Basic computer skills including knowledge in MS Outlook, of MS Word, Excel and typing skills. High School or Equivalent (Required) Hourly Rate range: Up to 23.50 hour Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Visit our careers site to read more about the benefits ICON offers. #LI-FL1 Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Salary range: - Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Are you a current ICON Employee? Please click here to apply

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Title: Clinical Research Scientist Duration: 12 Months (Possibility of Extension) Location Woodcliff lake NJ Job Responsibilities: The incumbent is responsible for, but not limited to the following: Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies Prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, ISE, Investigator Brochure, etc) Performs literature search and data analysis to address research questions In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct (enrollment, GCP practices, handling of safety issues, etc.) Assisting in database cleaning, review of study results, and interpretation of results Adhering to key performance indicators for clinical study development, conduct, and reporting Individual contributor with specialized knowledge Presents concepts, facts, and reports and advises on key trends and issues Troubleshooting routine site inquiries Work is completed under limited supervision Supports the planning, execution and reporting of clinical programs/trials May handle multiple protocols simultaneously Contributes to risk resolution by escalating and monitoring project risks Qualifications Qualifications Minimum of 2-5 years of experience in clinical research in the pharmaceutical industry A thorough understanding of clinical research methodology including study design, protocol writing, and CRF preparation is required, as is a knowledge of GCP and local regulatory requirements Working knowledge of the IND/NDA/CTD/MAA process acquired through direct industrial experience preferred Knowledge of medical, scientific and clinical research techniques in the oncology therapeutic area; Bachelor's Required. Doctoral (PharmD or PhD) or MD degree preferred . Additional Information Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus Thank you for your time and consideration. I look forward to hearing from you! Kind Regards Ruchi Kumari Clinical Recruiter Integrated Resources , Inc. IT Life Sciences Allied Healthcare CRO Certified MBE | GSA - Schedule 66 I GSA - Schedule 621I (DIRECT BOARD) # 732-844-8716 (F) 732-549-5549 LinkedIn: https://www.linkedin.com/in/ruchi-kumari Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Medical Technologists- levels I, II and Senior ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. * Medical Technologist multiple levels I, II, Senior - Farmingdale, NY ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development Job Title: Medical Technologists I, II and Senior Location: Farmingdale, NY- onsite Department: Our lab continues to grow, and we are currently seeking Medical Technologists for Hematology, Molecular and Immunology. Position Overview: We are seeking a talented and motivated Medical Technologist to join our Icon Central Laboratory team in Farmingdale, NY. In this role, you will play a key role in supporting our clinical research efforts by conducting laboratory tests, analyzing data, and ensuring compliance with regulatory requirements. Responsibilities: * Operate equipment carefully and according to procedures; maintain laboratory automation equipment per established operating procedures. * Perform necessary equipment checks, performance testing, preventive maintenance, and quality control on equipment per laboratory guidelines, as assigned. * Assure the accuracy of all tests performed by adhering to the laboratory's Quality Control Standard Operating Procedures. * Maintain complete documentation for assay tracking and results for review/reporting. * Complete the performance of proficiency testing in assigned laboratory sections. * Follow unidirectional flow of specimen handling to avoid contamination. * Good laboratory and organizational skills, including the ability to work independently and efficiently are essential. Qualifications: * NYS license as a Medical Laboratory Scientist required. * Bachelor's degree in Clinical Laboratory Science or similar degree preferred. * ASCP license as a Medical Laboratory Scientist preferred * Strong knowledge of laboratory techniques, instrumentation, and quality control procedures. * Experience working in a clinical laboratory or research setting is desirable. * Excellent communication skills and the ability to work effectively in a team environment. * Attention to detail, critical thinking, and problem-solving abilities. Salary: $33- $59 an hour * This is for the Farmingdale location only for levels I through Senior. Disregard compensation further below. Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Visit our careers site to read more about the benefits ICON offers. Benefits of working in a Clinical Research Lab vs Hospitals * Innovation and Discovery: Opportunities to contribute to cutting-edge research and potential breakthroughs in medical science. * Intellectual Stimulation: Engaging in hypothesis-driven experiments and problem-solving. * Professional Growth: At Icon, there are many ancillary teams associated with the lab, providing opportunities for career growth paths not just within the laboratory * Collaborative Opportunities: Instead of working closely with nurses, physicians, and caregivers you will be working with diverse teams, including program managers, Global Quality Control, Global Validations, Site Services, Specimen Management, Harmonization, Procurement, Quality Assurance, Data Integrity, as well as working with our three other global central laboratories. Similarities include: We utilize the same platforms that include Automated Chemistry with Abbott instrumentation. Our Special Chemistry department employs EIA and RIA instrumentation, as well as equipment from Roche, Siemens, and Optilite. For Automated Hematology, we use Siemens, Novus, and Stago platforms. Differences: Our lab primarily focuses on monitoring the health and safety of subjects within clinical trials, tracking their progress over multiple visits. #LI-FL1 Attachments * What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Salary range: $75,480.00-$94,350.00 Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Are you a current ICON Employee? Please click here to apply

IRI believes in commitment, integrity and strategic workforce solutions. Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity. Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success. Position: Network Engineer Duration: 1 + year - Possibility to go Temp to Perm Location: 999 Stewart Ave, Bethpage, NY DIRECT CLIENT: IMMEDIATE INTERVIEW Job Description: Provide network/LAN design, implementation and consulting for data and converged communications infrastructure based largely on Cisco equipment. Act as a trusted partner in implementing the data network infrastructure to improve business operations and customer satisfaction The Technical Services organization structure in which this position operates requires strong facilitation skills to sustain the teamwork, coordination and communication required among associates from multiple technical domains in order to deliver and maintain high quality services. While performing this role the candidate will be responsible for: • Collecting, consolidating and analyzing business and technical requirements from key constituents. Recommend appropriate technological designs and solutions that align with the business requirements, the company's technical strategy, and provides the most efficient and cost effective solution • Design, implementation, operation, and testing of a large scale enterprise Cisco based solutions • Data center network using virtualized Nexus switches, ASR Routers and ASA Firewalls • LAN/WAN using unified 3900 series routers and enterprise 4500/3800/2600 switching solutions • OSPF, BGP, MPLS, EIGRP, OTV, FCOE, LACP, LAG • Leading technical teams (including staff, vendors, and consultants) to identify and resolve complex, client application and hardware problems impacting availability and performance of the systems • Acting as the primary resource to client and IT staff in all phases of implementation and support process and provide high level support and consultation to business and IT management. • Working with project and development teams to ensure solutions are aligned with support requirements and that the transition and delivery of new systems or upgrades are seamlessly transitioned to production support teams and suppliers After hours callout is required in the performance of the duties and responsibilities of this position. Required Skills, Competencies, Education or Experience: • LAN/WAN routing and switching experience with Nexus equipment • Cisco certifications - Cisco Certified Network Professional (CCNP) Data Center or Route/Switch • Experience with Multicast, MPLS, OSPF and BGP routing protocols • Experience with Cisco Nexus, ASAs, VPN, IPS/IDS • Experience with Cisco 3900, 4500, 3800, 2900 • Experience with FCoE, FC and Cisco MDS 9000 · Strong communications, consultative and interpersonal skills, including oral, written and presentation; teamwork, collaboration, facilitation, and negotiation, with the ability to work effectively with internal client from various business organizations and lines of business, and IT management and staff. Desired Skills, Competencies, Education or Experience: • Cisco certifications - Cisco Certified Internetwork Expert (CCIE), Cisco Certified Design Professional (CCDP), Certified Information Systems Security Professional (CISSP). • Experience with and general understanding of some or all of the following: • NERC / CIP rules and procedures • Wireless communications and Licensed Radio technologies. • Project management. • Excellent analytical and problem solving ability • Understanding of general IT standards, policies, best practices, guidelines, processes. • Familiarity with Cisco UCS technology including UCS Manager, UCS Central and UCS Director • Ability to document and present material to Senior Level Management

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Project Manager II, Laboratory- Farmingdale NY- Blue Bell PA- hybrid The Project Manager, Labs will ensure client satisfaction by acting as the Client's main contact in all matters regarding ICON Laboratory Services (ILS), including the setup and day-to-day management of studies, attend and represent ILS at Client meetings, manage studies in accordance with Good Clinical Practice, provide Clients with regular study updates and communicate study progress to Clients and PM Leadership in a responsible and professional manner. The role * Act as the sponsor's main contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department. * Review newly assigned protocols and Amendments. Coordinate and manage the completion of the Clinical Laboratory Worksheet (CLW) and communicate information as required to other departments within ICON Laboratories (and ICON Clinical CRO if appropriate). * Enter protocol parameter information into PACS//ICOLIMS and other systems for new and/or amended protocols. Prepare and QC clinical study specific materials. * Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Ensure adherence to the protocol specific monitoring plan. Maintain clinical study specific study files and ensure that all appropriate documents are properly maintained. Ensure that all necessary documents are archived at study closure. * Provide Sponsors with study management reports. Provide client with support on ICOLabs system. Inform team leader about study progress. * Proactively monitor study budget. * Set the timelines for and monitor the progress of shipment requests for storage samples and verify data. * Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meeting, Bid Defenses or Initiations. * Develop new tools, train new employees. * Performs additional relevant responsibilities as requested by management. What you need * Bachelor's degree or local equivalent in Science, Business or related Field * Minimum of 2 years of experience working in a clinical laboratory, clinical trials, or customer management/account management role in a life science related organization * Minimum of 2 years of Project Management experience in a service area serving clinical trials, such as IVRS, Clinical Supplies Packaging and Distribution, Medical Imaging, Data Management, or Electronic Data Capture. * Working familiarity with Word, Excel, PowerPoint #LI-FL1 What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Salary range: $68,616.00-$85,770.00 Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Are you a current ICON Employee? Please click here to apply