Schlesinger Group jobs in Woodbridge, NJ - 395 jobs

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 Company provides contract development and customer support services to key health care customers, including hospital systems and group purchasing organizations, leading health plans, pharmacy benefit managers, and government health care institutions. The company also provides contract management, logistics and supply chain functions for the major franchises. The Commercial Payments team is responsible for the compliant, accurate, and timely calculation and processing of payments for multiple operating companies within the Pharmaceutical, Medical Device, and Consumer sectors. This individual will be responsible for reviewing and synthesizing large quantities of contractual material capturing the pertinent terms & conditions of the Commercial Payments team's payment obligations. Once the payment terms have been identified developing a means to track these terms will be required. Qualifications A minimum of a Bachelor's Degree is required. · A minimum of 5 years of knowledge/experience with various contract management systems and/or health care contracting policy is required. · Capable of reviewing, synthesizing large quantities of written contractual material is required. · Excellent communication is required. · Self-motivated, detail oriented, hands-on professional with initiative is required. · Understanding of and experience with systems and databases is required. · Proficiency in Microsoft Word, Outlook, Excel and PowerPoint is required. · Qualified candidates must be willing and able to work in Piscataway, NJ. Additional Information Warm Regards Parinita Bhintade HR Executive Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I (DIRECT BOARD) # 732-844-8731 (F) 732-549-5549 Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Hi , Hope you are doing well, I am sending you below job open with one of my direct client, if you are available in market, Send me your most updated copy of your resume in word document ASAP Job Title: Project Coordinator Duration: 8+ Months Location: New Brunswick, NJ Job Description and Responsibilities : • Candidate will be responsible for supporting the Global Talent Acquisition University Relations Manager in delivering comprehensive campus planning and logistics support through the University Relations department. • As part of the global support strategy, She/he will assist with the execution of company's International Recruitment Development Program, (IRDP), university relations strategy in order to recruit and hire the best talent for company. • Focus will be on enhancing company-wide university relations capabilities and strategies so as to promote company as the premier company of choice among external stakeholders as well as internal capabilities with stakeholders. • Provide support of IRDP's university relations strategy that may include advising with regards to recruiting sources; either administer or support key university relations programs; creation, review and reporting of university relations metrics and their effectiveness; and overall partner with regional university managers, Op Cos and any other relevant key stakeholders to execute IRDP university relations strategy. • Engage with key stakeholders to understand their individual transactional recruiting processes. Look for ways to automate those processes in a harmonized consistent way through the use of technology solutions. • Support the piloting of innovative, best-in-class university relations and talent identification tools with stakeholders, that will enable university Talent Acquisition to increase our ability to attract and recruit top talent and brand company as an employer of choice through on campus events, virtual events and regional global events • Collaborate with external suppliers to enhance service offerings that effect the overall productivity of recruiting teams through use of new technology tools (i.e., RECSOLU, InterviewStream, MBA Focus, MBA Exchange, ADP, Hogan, etc.) and university-specific IT systems to build better infrastructure capabilities. • Participate and contribute in meetings with key vendors to include The Right Thing, Inc. and RECSOLU in order to drive understanding of Talent Acquisition priorities and drive support of campus recruiting strategies. • Look for ways to streamline costs and hone efficiencies around campus recruiting practices, such as materials ordered, in support of recruiting activities. • Revisit current SOP's for ways to enhance or replace with alternatives, such as Virtual Event and InterviewStream technology upgrades, challenge vendors to provide premium services while economizing costs to the business. • Provide support for the International Recruitment Development Program (IRDP) stakeholders, participating in department meetings and lending support for key initiatives and increased support during the peak recruiting season. Requirements: • A 4 year accredited bachelor degree is required • Proficiency in Microsoft Office products including Word, PowerPoint, Excel • A minimum of 5 years work experience in a recruiting environment required • A strong knowledge of recruiting systems such as Taleo or similar applicant tracking system • Strong verbal and written communication skills are required to influence, inform and guide others • Possess excellent presentation skills and be comfortable participating and sometimes leading discussions with all levels of management • Strong analytical skills to translate data to insight and intelligence and action are required • Strong collaboration skills fostering credibility with clients and ability to partner, influence and support change with minimal direction as all levels • Open to 10% travel, sometimes internationally as required Additional Information Experience: 1-2 years relevant experience Bachelor's Degree preferred

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 Bench Scientific experience who can work independently. GMP Bioassays Has Elisa experience. Spectrometry and QPCR experience are a plus Qualifications Initiates, directs and executes all pre-clinical scientific research and/or development strategies in research and/or development. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems. Plans and executes laboratory research. Maintains broad knowledge of state-of-the-art principles and theories. May act as spokesperson on corporate research and development and advise top management. May participate in development of patent applications. Interfaces with various departments and serves as internal consultant. Additional InformationAll 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 The Clinical Research Associate for Clinical Operation will provide site monitoring and management oversight across multiple clinical research trials in support of development of Pharmaceutical's drug pipeline. This position will report to Associate Director of Clinical Operations and be responsible for operational support for clinical studies and related activities in accordance with company standard operating procedures, good clinical practice, and applicable regulatory requirements. JOB RESPONSIBILITIES: Support project management oversight of Clinical Development activities for multiple domestic and international trials, including: Track study timelines; Review and track study budgets; Provide periodic updates on Clinical Development Gradually develop responsibilities for management of contract research organization (CROs) activities for clinical and data management Provide monitoring support, in some cases functioning as the primary site monitor. Assist in writing and review of protocols, amendments, and informed consent forms. Manage development of study-specific guidelines (Case Report Forms, Monitoring Plans, and Pharmacy Manuals, etc.) Collaborate with Quality Assurance Department in development of Clinical Development standard operating procedures (SOP). Perform investigative site training Review CRO, vendor, and internal SOPs to ensure consistency and proper delegation of responsibilities among study teams. Assist in development of vendor relationships with CROs, drug depots, country-specific laboratories, and other vendors, as needed. Provide internal support for site recruitment activities. Oversee Trial Master File maintenance and reconciliation. Provide support to Regulatory Department in regulatory activities including submissions, and review of regulatory documents. Ensure compliance with FDA regulations and ICH Good Clinical Practice guidelines, as well as country-specific guidelines. Ensure compliance with study-specific procedures. Ensure compliance with study-specific procedures. KEY CONSIDERATIONS: Collaborate in a cross-functional environment in a small biotechnology company to assist in the initiation and coordination of global clinical initiatives and strategies. A strong background as a clinical research associate (CRA), specifically site monitoring or, alternatively; a nursing background would be noteworthy, particularly if the candidate has worked as a nurse at a research site. A therapeutic background to complement our pipeline, i.e. Cardiovascular, Hematology, Oncology, Pulmonology. Well-versed in Good Clinical Practices, medical terminology, and standard study procedures. Experience with electronic data capture systems. Good quality background and experience with healthcare or pharmaceutical development is required. Must be driven to deliver quality results on time and in a highly ethical and professional manner; Candidate must be willing to travel internationally (up to 25-50%, potential more depending on enrollment). Great organizational and communication skills. Proficient in use of Microsoft Office applications. Qualifications Thorough knowledge of Good Clinical Practice, clinical trial design, regulatory processes, and global clinical development process. 3-5 years of investigative site monitoring or study coordinator/study nurse experience. Hands-on experience in data cleaning and analysis required. Proven ability to work independently, to lead a multidisciplinary trial team. Proven experience in developing effective relationships with key investigators. Ability to maintain effective working relationships with coworkers, managers, as well as investigative site personnel. EDUCATION: Undergraduate Degree Additional Information Kind Regards Kavita Kumari Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I Direct Line : 732-549-5302 Ext 208 www.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 • Seeking dynamic, focused and creative individuals to join our growing team • Looking for experienced pharmaceutical professionals to help us build for the future. • Will be responsible for several portions of the adverse event case processing workflow including but not limited to receipt, evaluation, registration, partial data entry, documentation, and reporting of adverse event information from Clinical trial and post-marketing adverse event cases in accordance with company SOPs and US and worldwide regulations. Duties & Responsibilities- • Entry of AE information into the safety database, executing database queries and reports • Performing active follow-up via verbal or written contact with healthcare professionals (MDs, RNs, etc.) and consumers • Coding verbatim AE terms, medical history, laboratory data, and drugs using MedDRA and WHO-Drug dictionaries • Reconciliation of safety information received from external organizations, exchanged with corporate partners, and obtained from clinical trials • Train other department staff regarding handling of safety information as needed • Assist in compiling regulatory reports (e.g., PADER). • Perform other duties as required. Qualifications • Bachelor's degree. (In healthcare related field or with nursing background is ideal). • Strong interpersonal skills. • Strong process management and communication skills. • Working knowledge of drug safety reporting procedures and both US and international regulatory requirements. • Ability able to work both independently and under supervision to accomplish objectives within deadlines. • Minimum of 2 years' experience in drug safety. • Experience with safety database systems; Argus and MedDRA coding experience is ideal. Additional Information With Regards Ricky Bansal 732-429-1925

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 Our client is searching for a Systems Administrator. The individual will manage and tune in-house computer software systems and network connections to ensure high levels of availability and security of the supported business applications. This individual also participates in the planning and implementation of policies and procedures to ensure system provisioning and maintenance that is consistent with company goals, industry best practices, and regulatory requirements. RESPONSIBILITIES • Troubleshoot network systems and responds to issues and or problems. Provides documentation and management reporting. Provides tactical and strategic input on overall network planning and related projects. • Reviews, analyzes and evaluates business systems and user needs. • Installs new software releases, system upgrades, evaluates and installs patches and resolves software and OS related problems. Performs system backups and recovery. Maintains data files and monitors system configuration to ensure data integrity. • Provide user support as required. • Investigate network and security issues and provide recommendations for improvement. • Participate in Business Continuation/Disaster Recovery infrastructure planning, building, and testing. • Ensure the integrity and security of enterprise data • Manage end user accounts, permissions, access rights, and storage allocations in accordance with best-practices regarding privacy, security, and regulatory compliance. • Perform and test routine system backups and restores. • Anticipate, mitigate, identify, troubleshoot, and resolve hardware and software problems. • Support application development teams. • Analyze system, server, and application, and network, performance. • Recommend, schedule, and perform software and hardware improvements, upgrades, patches, reconfigurations, and/or purchases. • Conduct research on emerging products, services, protocols, and standards in support of systems software procurement and development efforts. • Develop, document, and maintain policies, procedures and associated training plans for system administration and appropriate use. • Build and deploy physical and virtual servers Qualifications EDUCATION This position requires a Bachelor's Degree in Computer Science, Information Technology, or related field and/or 10 years of relevant experience. Health Care or other relevant industry experience is preferred. SKILLS Required skills in order to perform the functions as a Windows System Administrator are as follows: • Experience with Windows server (2003, 2008, and 2012) platforms • Experience with Windows Security Configuration and Analysis • Experience with security tools/appliances (Firewalls, IPS) • Experience with Local Area Network technologies (Switches, Hubs, Routers, VPN, etc) • Working knowledge how to provide support for MS Active Directory including Windows domain group policies and administration • Experience with VMware • Experience with backup and recovery tools/software Additional Information Kind Regards surbhi khurana Technical Recruiter Direct Line : 732-429-1647 Board: 732-549-2030 - Ext 225 Website: www.irionline.com Integrated Resources, Inc.

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 1+ year of visibility inspection REQUIRED 1+ years of endotoxin testing and validations 1+ years of biologics background required Proficient in the performance of all Microbiology laboratory tests and assays Performs technical review of batch filling records to ensure quality of aseptic processes. Reads and interprets microbiological cultures and other related tests including but not limited to environmental monitoring, sterility tests, growth promotion, microbial limits tests and antimicrobial effectiveness tests Additional Information Regards, Indu Clinical Recruiter 732-844-8725 indu @irionline.com

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 This is a loan closing position responsible for coordinating document flow and loan closings for a growing portfolio of secured solar loans with a stable Fortune 500 utility company located in New Jersey. The successful candidate must be familiar with closing residential and commercial loans and must work well in a fast-paced environment. Key Duties · Communicate with loan customers as to closing procedures and answer customer generated questions and interact regularly with state agencies, legal department, and solar contractors. · Coordinate document flow and gather due diligence from closing attorney, borrowers and solar contractors · Review documentation received, solar technical data and site inspection reports for accuracy · Schedule loan closings with borrower · Calculate final loan amount based upon solar technical data and loan commitment amount. · Prepare funding information sheets detailing wiring information and disbursal of loan proceeds · Coordinate with Accounts Payable to process loan disbursals · Organize closing documentation, files and records Essential Qualifications: · Bachelor's degree or equivalent experience. · Minimum of 3 years of loan processing and/or loan closing experience · Knowledge of, or ability to learn quickly, the technical aspect of solar system production · Experience with records and file management · Strong computer skills; in-depth knowledge of MS Office (Word, Excel) and SharePoint Desired: · Basic knowledge of NJ SREC market · Previous experience working in the solar industry with familiarity with technical aspects of solar system generation Manager Must have · Documentation reading · Loan closing residential/commercial · SharePoint, power point, Excel preferred · Solar or utility exp preferred Qualifications Essential Qualifications: · Bachelor's degree or equivalent experience. · Minimum of 3 years of loan processing and/or loan closing experience · Solar or utility exp preferred Additional Information Kind Regards, Pramod Kumar Technical Recruiter Integrated Resources, Inc. DIRECT # - 732-844-8730

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: ETL Architect Location: NYC Duration: 6 months Job Description: This opportunity is for individuals who have Hands-on experience in data warehouse design and development. The Role demands more than a typical ETL lead role as it interacts outwardly on projects with architects, PM's, OPS, data modelers, developers, admins, DBA's and testers. This is a hands-on delivery-focused role, and the individual will be responsible for technical delivery of data warehouse and data integration projects Must have skills • 7-10 years Hands on experience with Informatica ETL in designing and developing ETL processes based on multiple sources using ETL tools • Experience in Architecting end to end ETL solutions • Hands on UNIX experience. Scripting (e.g. shell, perl, alerts, cron, automation) • Expert at all aspects of relational database design • Experience working with engineering team with respect to database-related performance tuning, writing of complex SQL, indexing, etc. Good to Have: • Experience with IDQ, MDM, other ETL tools • Experience with dashboard and report development • Experience with financial services firms will be preferred Additional Information Kind Regards Sachin Gaikwad Technical Recruiter Integrated Resources, Inc. Direct Line : 732-429-1920

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 Job Responsibilities • Analyze laboratory samples (raw material, in-process, finished product, stability, etc.) • legibly document the data and report the results associated with each analysis • Participate in laboratory investigations when required • Service laboratory equipment (calibrations, preventative maintenances, etc.) • Laboratory responsibilities can be assigned as deemed necessary • actively participates in the development of lower level Chemists (train, mentor & guide) • Comply with all applicable OSHA Safety and Health Programs • Adhere to all applicable cGXP regulations • Follow protocols, guidelines, procedures and methods as written • Obey all corporate systems and policies • Initiate and takes the lead role in Out-of-Specifications and Analytical Deviations of Quality Control Laboratory Investigations. • Ensure that products are being tested strictly under cGMP conditions and disposition is taken on time as per the committed Production Plan of every month (C to A, > 95%) and or procedural requirements • Troubleshoot laboratory equipment and methods • Helping to the Group Leaders in various aspects as and when needed. • Order and maintain all the Laboratory Chemicals and other needs of the Laboratory. • Hands on experience in handling analytical instruments like HPLC, GC, IR, UV, AAS, DSC, TGA, Malvern particle size • Knowledge on trouble shooting the Analytical Equipment • Performance of laboratory analyses correctly at the first time • Maintenance of the Analytical Equipment, the Analytical Columns and all other necessary things. Qualifications EDUCATION & EXPERIENCE: • 2- 4 years analytical experience in Pharmaceutical companies within the Quality Control / Quality Assurance environment • BS/MS in Chemistry, Pharmacy, Biochemistry or related field. • Experience in Generic Pharma. And Solid oral Dosage tablets / capsule highly desirable. Additional Information For more information contact me at 732-429-1921

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 Summary: Responsible for setting up clinical trials in the iDARTs application, an internally developed tool for medical review of clinical trial data based on TIBCO's Spotfire. At the trial level, perform the following activities: • Analysis, design and data mapping of new trials for iDarts At the Therapeutic Area level: • Contribute to the further improvement of our template library • Function as daily liaison between Clinical team members and the iDarts development and implementation team Responsibilities : • Analysis and design of iDarts for new studies • Design visualizations in line with study protocol specifications and translate them to specifications • Data mapping of iDarts for new studies • Map iDarts data visualizations to the clinical trial database. SDTM knowledge is a big asset. • User Acceptance Testing of iDarts • Test new study set-up in iDarts before release in to production • Team responsibilities for iDarts implementation • Help ensure that all new studies are set-up in iDarts on time. • Provide feedback where needed if questions arise during iDarts set-up • Function as liaison between Clinical team members and the iDarts development and implementation team • Identify additional needs for medical review, currently not supported by iDarts • Provide input to the iDarts IT group • Follow-up on needed improvements and changes needed EDUCATION & EXPERIENCE REQUIREMENTS: • BS/BA degree or professional experience equivalent • Good knowledge of TIBCO Spitfire • Minimum of 3 to 5 years of pharmaceutical or health care experience, including data analysis. • Good understanding of Clinical trials (including database structures & design) Additional Information Regards, Sweta Verma IT Recruiter Integrated Resources, Inc. “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (7th Year in a Row) Direct:- 732 549 5907 Tel: (732) 549 2030 x 210 Fax: (732) 549 5549 sweta(at)irionline.com https://www.linkedin.com/nhome/?trk=nav_responsive_tab_home

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 Working in the lab to develop liquid, semi solid or solid dosage form prototypes under the supervision of senior technical staff. Duties Include: Formulator with previous industrial experience developing generics. Ability to perform extensive Literature Search on assigned Projects. Familiar with adapting QbD (Quality by Design) elements in generic product development. Experience working with projects from bench-top stage to large scale manufacture of submission batches. Should have a sound knowledge of pharmaceutics, pharmacokinetics and process scale-up Qualifications MS or PhD in Pharmaceutics or related field. Additional Information Thanks Warm Regards, Sabanaaz Shaikh Integrated Resources, Inc

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: Network Security Analyst 6 months CTH • 3+ years of designing, implementing and supporting CISCO ISE is required Responsibilities: Work with vendor to ensure the quality design, implementation, installation/configuration, and provide technical admin support for Cisco ISE Authentication Authorization, Posture Assessment, and AnyConnect end point Malware Prevention solutions. • Upgrade Cisco ISE infrastructure including hardware, software, and AnyConnect • Perform Cisco ISE Authentication and Authorization • Enforce security Posture compliance for wired and wireless endpoints and enhance infrastructure security using the Cisco ISE • Deploy Cisco ISE Profiling and client provisioning services • Integrate Endpoint Malware Protection Services (AMP) with AnyConnect and Cisco ISE • Provide Reports, Monitoring, Troubleshooting, and Security Work with vendor on problem resolution Create policies and reports to meet the business requirements Participate in Planning, Design, and Tests Perform security audits, scan and monitor servers Investigate and report on security alerts and perform security incident reporting Requirements: Expert-level knowledge and experience with design, implementation and support of Cisco ISE 3-5 year of experience working with Network Security applications Complex routing and switching solutions (Cisco is a must, Nexus strongly preferred, other manufacturers are a plus) Advance knowledge of networking, TCP/IP, FTP, SCP, firewalls, ACLs, Authentication protocols, Authorization, VPN, PKI, RSA, and Encryption Knowledge of Directory Services including Active Directory, LDAP, and TDS Knowledge of F5 load balancers Knowledge of IT security principles, HIPAA, SOX and PCI regulations Knowledge of IDS/IPS, Malware Prevention (Sourcefire & Fireye desired, Palo Alto a plus) Business Analysis skills and ability to translate business requirements into technical requirements Excellent oral/written communication and organizational skills Security certification a plus such as CISSP, CEH or CISA Qualifications Bachelor's Degree in Computer Science, Programming, or IT required Additional Information Contact- 732-549-2030 ext 242 Harshad

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 aretas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description • The Clinical Research Associate for Clinical Operation will provide site monitoring and management oversight across multiple clinical research trials in support of development of Client's drug pipeline. • This position will report to Associate Director of Clinical Operations and be responsible for operational support for clinical studies and related activities in accordance with company standard operating procedures, good clinical practice, and applicable regulatory requirements. Requirements- • Support project management oversight of Clinical Development activities for multiple domestic and international trials, including: • Track study timelines • Review and track study budgets • Provide periodic updates on Clinical Development • Gradually develop responsibilities for management of contract research organization (CROs) activities for clinical and data management • Provide monitoring support, in some cases functioning as the primary site monitor. • Assist in writing and review of protocols, amendments, and informed consent forms. Manage development of study-specific guidelines (Case Report Forms, Monitoring Plans, and Pharmacy Manuals, etc.) • Collaborate with Quality Assurance Department in development of Clinical Development standard operating procedures (SOP). • Perform investigative site training • Review CRO, vendor, and internal SOPs to ensure consistency and proper delegation of responsibilities among study teams. • Assist in development of vendor relationships with CROs, drug depots, country-specific laboratories, and other vendors, as needed. • Provide internal support for site recruitment activities. • Oversee Trial Master File maintenance and reconciliation. • Provide support to Regulatory Department in regulatory activities including submissions, and review of regulatory documents. • Ensure compliance with FDA regulations and ICH Good Clinical Practice guidelines, as well as country-specific guidelines. • Ensure compliance with study-specific procedures. Key Considerations- • Collaborate in a cross-functional environment in a small biotechnology company to assist in the initiation and coordination of global clinical initiatives and strategies. • A strong background as a clinical research associate (CRA), specifically site monitoring or, alternatively; a nursing background would be noteworthy, particularly if the candidate has worked as a nurse at a research site. • A therapeutic background to complement our pipeline, i.e. Cardiovascular, Hematology, Oncology, Pulmonology. • Well-versed in Good Clinical Practices, medical terminology, and standard study procedures. • Experience with electronic data capture systems. • Good quality background and experience with healthcare or pharmaceutical development is required. • Must be driven to deliver quality results on time and in a highly ethical and professional manner; • Candidate must be willing to travel internationally (up to 25-50%, potential more depending on enrollment). • Great organizational and communication skills. • Proficient in use of Microsoft Office applications. Qualifications • Thorough knowledge of Good Clinical Practice, clinical trial design, regulatory processes, and global clinical development process. • 3-5 years of investigative site monitoring or study coordinator/study nurse experience. • Hands-on experience in data cleaning and analysis required. • Proven ability to work independently, to lead a multidisciplinary trial team. • Proven experience in developing effective relationships with key investigators. • Ability to maintain effective working relationships with co-workers, managers, as well as investigative site personnel. • Undergraduate Degree Field of study: Health/Life Sciences, Medical Technology, Biochemistry, or Microbiology. Additional Information Warm Regards Ricky Bansal 732-429-1925

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 • Seeking dynamic, focused and creative individuals to join our growing team • Looking for experienced pharmaceutical professionals to help us build for the future. • Will be responsible for several portions of the adverse event case processing workflow including but not limited to receipt, evaluation, registration, partial data entry, documentation, and reporting of adverse event information from Clinical trial and post-marketing adverse event cases in accordance with company SOPs and US and worldwide regulations. Duties & Responsibilities- • Entry of AE information into the safety database, executing database queries and reports • Performing active follow-up via verbal or written contact with healthcare professionals (MDs, RNs, etc.) and consumers • Coding verbatim AE terms, medical history, laboratory data, and drugs using MedDRA and WHO-Drug dictionaries • Reconciliation of safety information received from external organizations, exchanged with corporate partners, and obtained from clinical trials • Train other department staff regarding handling of safety information as needed • Assist in compiling regulatory reports (e.g., PADER). • Perform other duties as required. Qualifications • Bachelor's degree. (In healthcare related field or with nursing background is ideal). • Strong interpersonal skills. • Strong process management and communication skills. • Working knowledge of drug safety reporting procedures and both US and international regulatory requirements. • Ability able to work both independently and under supervision to accomplish objectives within deadlines. • Minimum of 2 years' experience in drug safety. • Experience with safety database systems; Argus and MedDRA coding experience is ideal. Additional Information With Regards Ricky Bansal 732-429-1925

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 Position: SSIS developer Location: Jersey City, NJ (must be onsite 5 days/wk, no travel reimbursement or remote work) Duration: 3+ Months Required skills: 1. 10 or more years' experience in database and data integration 2. SSIS data integration in SQL Server *AND* Oracle DB environments 3. C# development 4. SSIS Custom Component development Optional skills: 1. Experienced in the full System Development Life Cycle (Dev, Test, Prod) 2. Proficient in SQL, Oracle PL SQL 3. Good in Batch scripting and Power shell scripting 4. Excellent communication skills 5. Proven ability to work in a dynamic team environment Qualifications 10 or more years' experience in database and data integration Additional Information Thanks Warm Regards Harshad Integrated Resources, Inc IT REHAB CLINICAL NURSING Inc. 5000 - 2007-2014 (8th Years) Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70 (732) 429 1922 Edison NJ 08817

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 Looking for a Project Coordinator I for the Raw Material Center/Packaging Material Center. This individual will work with cross functional teams on Supplier Related Changes and governance of materials and suppliers. The Project Coordinator will be responsible for managing both Chemical and Packaging Supplier Change Controls ensuring timely closure. This position is located in Skillman, NJ. • Strong analytical and organizational skills • Strong relationship building and negotiation skills • Ability to effectively communicate and work in matrixed environment • Ability to identify and report trends/emerging issues in a timely manner • Ability to translate findings into recommended actions • Technical background a plus; some understanding/ limited experience relating to chemicals and packaging components preferred • Ability to collaborate in team environment and work independently when required • Ability to multitask • Project Management/Coordination experience strongly preferred Project Coordinator I Deliverables: • Leading the coordination of project activities to ensure timely project closure • Delivering projects of varying complexity in timely manner • Completing all relevant trainings for the assigned tasks timely • Owning, driving, and being accountable for assigned processes with regularly updated reports • Writing and deploying procedures associated with the assigned business processes • Establishing and/or maintaining business performance metrics for the key assigned business areas • Conducting daily business activities in accordance with the foundation of J&J Credo Project Coordinator I Qualifications: • A minimum of a Bachelor's degree is required. A focused degree in Science, Engineering, Business, or a related field is preferred. • One year or more of experience coordinating projects required Additional Information Regards, Sweta Verma IT Recruiter Integrated Resources, Inc. Inc. 5000 - 2007-2014 (8th Year) Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70 (Direct) 732 549 5907 | (W) 732 -549 - 2030 x 210| (F) (732) 549 5549

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 Acquisition & Deployment • Design and deploy company LANs, WANs, and wireless networks, including servers, routers, hubs, switches, UPSs, and other hardware. • Conduct research on network products, services, protocols, and standards to remain abreast of developments in the networking industry. • Oversee new and existing equipment, hardware, and software upgrades. • Interact and negotiate with vendors, outsourcers, and contractors to secure network products and services. Operational Management • Configure networks to ensure their smooth and reliable operation for fulfilling business objectives and processes. • Monitor network performance and troubleshoot problem areas as needed. • Oversee installation, configuration, maintenance, and troubleshooting of end user workstation hardware, software, and peripheral devices. • Ensure network connectivity of all servers, workstations, telephony equipment, fax machines, and other network appliances. • Assist in managing servers, including database, e-mail, print, and backup servers and their associated operating systems and software. • Practice network asset management, including maintenance of network component inventory and related documentation and technical specifications information. • Monitor and test network performance and provide network performance statistics and reports. • Participate in managing all network security solutions. • Perform server and security audits, and system backups and recovery. • Manage and/or provide guidance to junior members of the team. • Knowledge & Experience • Proven experience and success with LAN, WAN, WLAN, and WWAN design and implementation. • Proven experience with network capacity planning, network security principles, and general network management best practices. • Strong, hands-on technical knowledge of network and PC operating systems, including Windows, Linux, Sun/Solaris. • Excellent knowledge of telephony systems, including IP based systems design and deployment. • Working technical knowledge of current network hardware, protocols, and Internet standards, including Cisco 6500, Cisco ASA, Cisco IPS, routers and switches. • Excellent hardware troubleshooting experience. • Extensive support experience with Qradar, Fireeye, Fluke, Veronis, Mcafee/EPO, Mailgate, Websense, Sophos, or similar tools. • Experience with unified communication and mobile worker support • Competence scripting and automating support functions • Competence with diagnostic/testing tools and procedures for voice and data circuits. • Good understanding of the organization's goals and objectives. • Knowledge of applicable data privacy practices and laws. EDUCATION/EXPERIENCE/PERSONAL REQUIREMENTS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The core competencies listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Formal Education & Certification • University degree in computer science or electrical engineering and/or 10-15 years equivalent work experience. • Certifications in Cisco Networking (CCEI, CCNP, or CCNA) preferred. 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

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 • The Analytical R&D Chemist will support the Formulations Group in developing and validating analytical methods for raw materials and finished products, reverse engineering of formulation components and analysis of stability samples. • The position will be primarily laboratory based and requires a strong background in chromatography and preferably in semi-solid dosage forms • The candidate will have a proven track record developing and validating GMP-compliant HPLC & GC methods to assess drug substance and product stability, have experience diagnosing and troubleshooting HPLC instrumentation • The scientist will routinely interact with other laboratory personnel, and will interact with vendors, customers, and business partners as necessary • Prepares technical documents, including method development/validation protocols and reports, analytical test procedures, technical reports, change controls to support FDA submissions • Executes method development and validation protocols for finished products • Reverse engineer formulation components using sample preparation and analytical procedures. • Evaluates the chemical and physical attributes of finished products such as pH, viscosity, water content, assay and content uniformity • Maintain the analytical lab including calibration, performance maintenance and log books • Ability to analyze, interpret and troubleshoot data • Follow Company's SOPs and ensure cGMP compliance • Assists in the investigation of OOS/QR and OOT data and assist in writing investigative documents • Responsible for maintaining laboratory housekeeping, cleanliness of laboratory equipment and workbenches, and other general lab responsibilities as assigned by supervisor • Might require to work on extended hours on an as-needed basis Qualifications • B.S./M.S. in chemistry, pharmacy or related discipline with 2+ years related experience • Previous experience in a cGMP laboratory setting • Ability to handle multiple projects, efficiently and timely manner • Knowledge of the generic industry, including ANDA submission • Experience with topical and ophthalmic products is preferred • Ability to work in a dynamic working environment Additional Information Thanks Warm Regards Ricky Bansal 732-429-1925