Integration International jobs - 232 jobs

Integration International Inc. (I3), we are an IT Solutions and Consulting Services company with a track record of executing global infrastructure projects. We are privately-owned and part of a group of companies having registered offices in China, Belgium, UK, Canada, India and our HQ is in New Jersey. We function as a global services arm for all our group cos and are technology independent. Our seamless blend of Applications, Infrastructure and Professional Services enables clients to maximize returns on their IT investments. Through collaborative and strategic partnership model, we deliver intangible value to clients using innovative ideas, best practices and diverse technology expertise. Job Description Job title: Sales Representative Job location: Parsippany, NJ Duration: Full-time Responsibilities: · Market and sell our suite of services by prospecting and acquiring new clients to increase our client base. · Schedule appointments with prospective clients utilizing multiple communication channels (phone, email). · Develop relationships with potential and current referral sources, gaining referrals to prospective clients. · Strive to consistently gain technical, competitive and sales skills knowledge. Qualifications Qualifications: High School Diploma (BA/BS preferred) in business or related fields 2-4 years relevant sales experience (payroll related sales experience preferred) Possess a strong work ethic, initiative, positive attitude and high energy Aptitude towards organizing projects, multi-tasking Excellent attention to detail Excellent communication skills, both verbal and written Additional Information Rachel Shah Resource Deployment Executive Integration International Inc. ************

Integration International Inc. is an IT Solutions and Professional Services Company globally HQ in Parsippany, NJ. We offer Application Services, Infrastructure Services and Staff Augmentation Services to Fortune 1000 companies across North America. Our direct Clients are leading names in Banking, Finance, Manufacturing, Publishing, Life Sciences, Technology and Services industry verticals. Please visit us at ************** for more info. Job Title: Call Center Bilingual Customer Service Rep Location: Mercerville, NJ 08619 Duration: 6+ Months (Possibility of extension) JOB DESCRIPTION : Provides information to customers regarding department/agency programs and services and the requirements of licensure, certification, and other authorizations Answers questions, explains rules, regulations, policies and procedures, clarifies forms, provides instruction and direction in the completion of applications, and resolves issues and problems Requests information from customers to determine their needs, or purpose of visit Verifies the completeness and accuracy of information on forms and applications Conducts information searches in electronic or manual file systems Ability to read, writes, speak, understand, or communicate in English and Spanish sufficiently to perform the duties of this position. Required 3 years of customer service experience on the resume. Must be recent. HS or higher Bilingual English/Spanish Required Additional Information Thanks & Regards, Sophia Chawhan Resource Deployment Executive Integration International Inc. Direct#-************ .

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Responsible for implementing regulatory strategy and managing operational activities for assigned regions. Provides input into global regulatory strategy, including identification of gaps or risks in global strategic plan for assigned regions. Partners with regions to align on regulatory strategy in order to fulfill business objectives Represents DRA on or leads sub-teams as required. Determines requirements and sets objectives for Health Authority (HA) interactions with regulatory lead Facilitates preparation and finalization of briefing books and contributes to preparation of summary documents. Develops and implements plans for timely response to HA requests and coordinates responses. Drives coordination, planning, and submission of dossiers in assigned regions worldwide. Review of global dossier summary documents. Reviews, approves and submits Clinical Trial Applications (CTAs) and Investigational New Drugs (INDs). Responsible for finalization and on time submission of annual reports and renewals across assigned regions. Responsible for appropriate entering and quality of product specific attributes in compliance database. Ensures regulatory compliance for project and keeps records of all major HA interactions in the validated document management system. Ensures quality and compliance with global regulatory requirements (regions responsible) and adherence to regulatory internal policies and processes. Skills: Prior 2-4 years of regulatory experience required, ideally in US or EU Strong knowledge of regulatory submission and approval processes, ideally in US or EU Strong interpersonal, communication, negotiation and problem solving skills. Prior history with post-marketing/brand optimization strategies and commercial awareness preferred. Proven ability to analyze and interpret efficacy and safety data. Regulatory operational expertise Qualifications Science based BS or MS with requisite experience and demonstrated capability. Additional Information Richha Saini Senior Clinical/Scientific Recruiter 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides te chnical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Job Description • BA/BS in a quantitative sciences field (mathematics, statistics, operations research, econometrics, engineering, or similar) • Experience in developing and applying quantitative or analytical modeling techniques to business problems in the pharma, Client, or financial services industries • Advanced Excel & PowerPoint skills • Demonstrable experience in implementing and embedding new processes & ways of working • Solid understanding of database structure, design and reporting principles Preferred Requirements • Advanced degree in quantitative sciences field &/or MBA • Experience in portfolio management in a pharma / Client environment • Experience in resource management and/or capacity planning in a pharma / Client environment • Proven success in design and implementation of technology-enabled business solutions • Proven track record as key business partner with IT, delivering challenging projects to time and budget • Strong project management, influencing, communication, technical skills and innovative / flexible thinking • Highly developed interpersonal, influencing, negotiating, communication and relationship-building skills across all levels of an organization • Independent and fast learner, able to prioritize and manage multiple tasks • Commitment to excellence and continuous improvement - evidence of challenging the status quo and developing new approaches to existing ways of working • Demonstrated leadership in the external portfolio management community; leading, inspiring and motivating a globally matrixed team Qualifications Key responsibilities We are looking for a highly numerate, structured thinker with great interpersonal skills to join our global portfolio management team to help embed and maintain a newly-implemented resource planning capability within our global R&D organization. In order to achieve this you will need to: • Take ownership of key resource planning systems and processes • Build and maintain interactive relationships with key stakeholders across the R&D organization • Maintain related communications and support material • Provide timely support to queries from colleagues relating to resource planning process • Ensure the availability of timely and accurate information regarding allocation of resource for key decision-making forums • Build awareness of resource planning capability embed across all relevant teams & functions • Contribute to ad hoc analyses regarding allocation of resource and resulting internal expenditure • Partner with IT and 3rd party suppliers regarding maintenance and potential improvement of resource planning system; taking into account dependencies on other key R&D systems • Input into regular KPI reporting processes • Support discussions regarding evolution of portfolio management capability and related systems • Partner with Finance to ensure mandatory reporting requirements are fulfilled; and to support development of project costing approach Additional Information For more information, Please contact Shobha Mishra ************ Shobha.MishraATartechinfo.com

Purpose/Objective of the job Support Medical Safety Assessment Physicians (MSAP with cross-functional Medical Surveillance Teams (MSTs) and assigned subteams, such as Safety Data Review (SDR) Teams. Appropriately elevate program or portfolio issues impacting key MST programs, priorities, resources, milestones. Contribute to regulatory documents and assist with projects. Key Responsibilities and Major Duties 1. Participate in cross-functional Medical Surveillance Teams (MSTs) and assigned subteams, such as Safety Data Review (SDR) Teams, and participate in related PV and product-development subteam(s). Appropriately elevate issues impacting key MST activities, milestones, documents to the MST Chair. 2. Periodic review of pertinent safety-related literature, analysis of pre-determined core signal data. Provides advice and summaries, evaluations and conclusions of safety data reviewed. 3. Collaborate within and across BMS functions with appropriate disciplines to identify and ensure management of internal and external documentation and support when required. 4. Apply knowledge of product goals, strategy, drug development stage milestones, partnership agreement, HA commitments, and individual functional area responsibilities. Mentor individuals and teams on these applied learnings. 5. Coordinate and integrate scientific, medical, and regulatory input from a variety of scientific sources and functional groups, as needed to support responses to ad hoc queries and HA commitments. Contributing to and authoring regulatory documents. Qualifications Manager is looking for someone with data analysis, literature review, PBRER writing, aggregate report writing. Additional Information Interested candidates may contact at "Praveen.arora(@)artechinfo.com or ************"

Artech Information System , a global staffing and IT consulting company. We are constantly on the lookout for professionals to fulfill the staffing needs of our clients and we currently have a job opening that may interest you. Job Title: Safety Specialist/Sr. Triage Associate Job ID: 21435-1 Location: Pennington, New Jersey- 08534 Duration: 6+ month with potential for extension Ideal candidate will be a Nurse with PV experience Job Description: Sr. Triage Associate/ Safety Specialist Department Title and Description Case Creation/Triage Purpose/Objective of the job Lead subject matter expert in prioritizing cases and entering critical data in order to meet regulatory reporting responsibilities. Key Responsibilities and Major Duties • Accountable for incoming reports and information contained therein to determine the seriousness of the report, determine contractual responsibilities in order to assign a regulatory due date. • Accountable for identification of all related clinical study cases for Semi-annual report of Suspected Unexpected Serious Adverse Reaction (SUSAR) • Accountable for identification of potential signal detection cases and communicates this to the Medical Review Safety Physician (MRSP). • Organizes work load in order to prioritize the most urgent deliverables (i.e. reports) ultimately to execute accurate reportable timelines • Utilizes knowledge of specific work practices, Safety Data Exchange Agreement (SDEA), Standard Operating Procedures (SOP), and regulations in order to process cases in a timely manner and lead the team to execute the process appropriately. • Seeks to understand and adhere to SDEA in processing cases involving products under co-marketing arrangements in order to handle all cases in a timely manner. Serves as a resource to identify CLIENT products and designated co-marketers. • Incorporates medical and fundamental complex understanding of the human anatomy and its functions in order to process adverse event reports in an accurate and consistent manner. • Oversees that all follow up cases go into the appropriate case based on ICSR and also liaises with MRSP if needed. • Develop and execute training for alignment in processing. • Accountable for multiple tasks, prioritizes tasks according to designated criteria and remains flexible as processes and priorities change. • Exercises a high degree of adaptability in dealing with an ambiguous and complex work environment, which includes demands not only from respective teams, but also from regulatory agencies, co-marketing partners and the GPV&E Medical staff. • Serves as a trainer, mentor, and guide for colleagues within GPV&E through providing perspective on the broad organizational impact on their daily work. • Coordinates the daily responsibilities and workload of the team by deploying resources and delegating appropriately and equitably in order to meet short term and long term goals defined for adverse event processing. Triage Associate and Senior Case Processor work directly with Sr. Triage Associate to get core daily work responsibilities completed. Sr. Triage Associate directs the team to prioritize cases and special projects and delegates when needed. List of minimum requirements • Degree/Certification/Licensure Bachelors degree, Master degree Preferred, scientific/medical background (B.S./B.A, M.S.) in Life Science, Nursing, Regulatory Affairs, Chemistry or Pharmacy Experience - Responsibility and minimum number of years • Minimum of 8 years pharmaceutical experience with a strong preference of 5 or more years in pharmacovigilance, drug development, clinical development, quality and/or regulatory. Competencies - knowledge, skills, abilities, other Mastery of health / life sciences gained through either formal education or on job experiences. • Mastery of AE processing both internally and externally, as well as the ability to understand the future impact. • Mastery of the intricacies of AWARE (the CLIENT drug safety database). • Knowledge of CLIENT drug development and commercialization process and the impact of AE Processing on that process. • Knowledge of general safety reporting requirements, regulations, guidelines and procedures. • Experience working with a wide range of technically and culturally diverse people and influencing them to accomplish a common goal. • Experience utilizing problem solving techniques to ensure that AE reports are available for processing at the earliest possible time. • Experience supervising a team. • Experience communicating to a diverse audience, at multiple levels through various formats (i.e. presentations, meetings, proposals, face-to-face meeting). • First hand experience working directly with customers, technical experts and professional staff. Software that must be used independently and without assistance (e.g., Microsoft Suite) Additional Information All your information will be kept confidential according to EEO guidelines.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description POSITION:DESKTOP SUPPORT LOCATION: WHITEHOUSE,NJ Duration:1+years · Deskside Support Tech. · Must be experienced in DESKSIDE support, Remote / CTS Support, SCCM, Windows, Incident, IMAC, VDI, SW/Break/fix, IMAC. · Ability to solve tickets remotely, work with SCCD. Reply Asap. Additional Information For more information, Please contact Shubham ************

Artech Information Systems is the #12 Largest IT Staffing Company in the U.S. and an employer of choice for over 7,000 consultants. We recruit world-class talent for IT, engineering, and other professional jobs at 70+ Fortune and Global 500 companies coast-to-coast across the U.S., India, and China. We are one of the fastest-growing companies in the US and we welcome you to search the thousands of jobs in our cutting-edge GEM system for employment opportunities that fit your qualifications. At the forefront of the staffing industry, Artech is a minority and women-owned business enterprise (MWBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured long-term partnerships with Fortune 500 and government clients seeking world-class professional resources. Job Description 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, Client, 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 • Minimum of 5-7 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) degree preferred Qualifications BS/MS Additional Information For more information, Please contact Best Regards, Akriti Gupta ************** Morristown, NJ 07960

Artech Information System , a global staffing and IT consulting company. We are constantly on the lookout for professionals to fulfill the staffing needs of our clients and we currently have a job opening that may interest you. Job Description Job Title: Coordinator Job ID: 21335-1 Location: Pennington, NJ-08534 Duration: 6+ months with potential for extension Description: · Uses administrative and organizational skills to support a team function or management. · Essentially organizes and controls data and records for project execution or records submission and retention. · Conduct limited research Performs additional general office duties as assigned Create and manage supervisor Travel and Expense Reports · Create Track purchase orders Arrange meetings and teleconferences for dept. · Basic calendar management for supervisors · Prepare ad hoc reports for management' Skills: · An understanding of U.S., EU and ICH safety reporting regulations and guidelines is desirable · Skills in document management and electronic document publishing skills is desirable · Must have strong computer skills (Microsoft Office Suite and Adobe Acrobat) · Must have great organizational skills and effective communication · Experience Working in a Team Environment · Capable of working independently on multiple projects in timely manner focusing on customer deliverables · Must be detail oriented with strong organizational skills and work efficiently to achieve results in a timely fashion Knowledge of Safety Database is required. Additional Information All your information will be kept confidential according to EEO guidelines.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Development of processes and identify and qualify new business opportunities. This role links closely with R&D to leverage technical possibilities and understand technical trade-offs vis a vis market potential. Works closely with market research group to Client new consumer/ patient insights. As initiatives advance toward market launch, this role will also support the development of the winning consumer & ECP big idea, and lead concept, claims, key benefit and RTB visuals, as well as any relevant sights & sounds cues. It is crucial the candidate has global experience as well as innovation, new product development, and/or new product launch experience. This individual must be proficient in market landscape assessment, analyzing diverse market segments and providing recommendations on new market opportunities. This position also supports Client&L in the scouting and due diligence processes with market assessment, conception and financial calculations. 1. Responsible for safety issue management from end of Phase I (POC) through Life Cycle Management. 2. Accountable for overall signal detection, monitoring, evaluation, interpretation and appropriate management of safety information, based on information from all relevant line functions, post marketing data, and other sources. 3. Accountable for developing and updating, at milestones, the safety profiling and risk management plan from end of Phase I (POC) through Life Cycle Management, as relevant. Accountable to ensure adequate risk management plans are in place. 4. Leads Safety Management Team. 5. Serves as safety representative as core member of Global Program Teams. Manages Drug Safety Monitoring Board activities for assigned projects/products, as required. 6. Accountable for responses to inquiries from regulatory authorities or health care professionals on safety issues. Accountable for safety data for health authority review boards. Accountable for responses to legal queries and CPO requests involving safety issues. Ensures safety information communicated to EU Qualified Person in a timely fashion. Coordinates product-specific activities. 7. Accountable for integrated safety input into all safety relevant parts of regulatory and company documents (i.e. IB, CDS, SCS, RMP, SPP, CO, PIP, GDPS, CDP, etc.) required during active development, submission phase and during marketing phase. 8. Review of medical safety input into study protocols (including MRC and OPCE) MAP, RAP and ICF. 9. Review/approve product-specific safety deliverables: IN letter, PGD, data searches, literature review, expert statements. 10. Coordinates involvement of external experts (e.g. authors of "white papers," members of trial-specific data safety monitoring boards, ad-hoc support for HA meetings, etc. 11. Accountable for presentations on project/product safety issues to internal Client Boards, or expert panels and other meetings. 12. Collaborates productively and manages in a cross-functional matrix team environment (e.g., SMT). 13. Assist in training of new hires (e.g. new BSLs) and mentor/coach direct reports (PVL/PVE) as required. 14. Provides support as needed for licensing activities, regulatory authority inspections and for project/product recall activities. 15. Serves as and performs activities of Pharmacovigilance Leader such as ad-hoc medical case review as needed. Skills: Three years medical experience postdoctoral o At least five years in industry or health authority or CRO (of which two years in a global position), including a minimum of three years in drug safety o Experience in preparing clinical safety assessments, risk/benefit evaluations and regulatory reports o Experience in leading cross-functional, multi-cultural teams o Experience in preparing RMPs, PSURs, submission dossiers (SCS) Qualifications MD Required Additional Information Thanks Richha Saini Technical Recruiter Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ "2014 Service Excellence Award Winner from J&J"

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description 1. The incumbent will have responsibility to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements, the Client Pharma Corporate Quality Manual and Policies, and site procedures and business requirements. 2. Coordinates and performs batch record issuance for internally manufactured products Reviews and approves manufacturing and QC related documents for raw material disposition. 3. Reviews and approves manufacturing and QC related documents for manufactured media Performs administrative functions for filing and maintenance of records between QA operations and Document Control Center Support cGMP and associated OJT training to QA and other departments to improve right the first time (RTFT), high quality performance. 4. Control costs within department to meet budget. Complete job-related training in electronic database system along with GMP, safety, and Ethics & Compliance course requirements. 5. Perform or support any other tasks necessary to maintain the product quality and site cGMP compliance, as needed. Skills:0-3 years GMP manufacturing and/or QA related experience 6. Education: BS/BA in Biological Sciences or equivalent relevant career experience Additional Information Regards, Anuj Mehta ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Include tracking of activities provided by external contract laboratoreis both clinical and pre clinical. Ensures all necessary documentation is inmplace (ie statements of work/assay development requirements etc). Additional responsibilities include reviewing/distributing all external research reports. Additional Information Regards, Anuj Mehta ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Position:Deskside technicians or data entry specialist Location: Mahwah NJ Duration:1year · The technicians responsibilities will consists of data entry and also to monitor the Dispatch call in number to assist dispatched technicians in the field with installations, moves, incidents etc.. · Training will be provided the first 2 weeks during regular business hours. Additional Information For more information, Please contact Shubham ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Service Availability Manager Infrastructure Services-Availability Management required Additional Information For more information, please contact Shubham ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description At least 5 years of pharmaceutical experience at Ph.D. level (or 8 years at MS level ) in biostatistics, statistics and epidemiology Excellent communication skills (verbal and written) Good team player Advanced level in SAS but not looking for a SAS programmer. Looking for a senior level statistician who is advanced in SAS programming. Additional Skills Extensive experiences in phase III trials, in particular, CV trials, for example familiar with statistical analysis plan, clinical study report, database, analysis data sets and statistical programming specification. Experiences in worldwide submission, in particular, PMDA in Japan providing statistical analysis for ad hoc requests Strong statistical training, in particular, survival analysis Leadership (establish priorities and objectives, implement actions and plans and always look for solutions independently) Proactive communication with project team members. Preferably some oncology experience Additional Information Best Regards, Anuj Mehta ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description The Pharmacovigilance Scientist (PVS) will serve as a core member of the safety team and is responsible for performing proactive pharmacovigilance activities on a product, or group of products in a therapeutic area or franchise, in partnership with the Global Safety Officer (GSO) to evaluate safety data and signals for both marketed products and products in clinical development. This includes performing signal detection and safety management committee activities, authoring safety evaluations, contributing and reviewing of aggregate safety reports, assisting with ad hoc regulatory responses, facilitating signal management process for assigned products (i.e., signal tracking, data analysis, leading review meetings, presenting, etc.) in collaboration with the GSO and Pharmacoepidemiology. Additionally, the PVS will support the GSO with other safety related activities associated with new drug applications / regulatory filings, benefit risk assessment and safety risk management and support activities related to risk minimization including dRMP/RMP and REMS. The PVS will provide coordination and oversight to outsourced activities (i.e., signal detection reports, clinical overviews). Good knowledge of pharmacovigilance practices Good knowledge of US and EU pharmacovigilance regulatory requirements Excellent written and verbal communication skills Ability to present and critically discuss safety data in both internal and external discussions Ability to evaluate, interpret and synthesize scientific data (analytical thinking) Team player with ability to function in a cross-functional environment Self-motivated, able to prioritize and plan effectively, and independently, with minimal supervision Fluent in English (verbal and written) Good moderator skills Ability to navigate in databases and pull information correctly Good organizational skills and attention to detail Education: Minimum Bachelors of Science or Health Care Professional (RN, BSN, Nurse Practitioner or Physician Assistant, RPh); or preferred advanced health care discipline degree (MDPharmD, PhD, Masters of Science, etc.) or equivalent qualification. Required Experience: Basic knowledge of common data processing software (i.e., Excel, PowerPoint, Word) and database systems Additional Information Best Regards, Anuj Mehta ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description This role is key for medical supervision and medical management of clinical trials proposed or to be performed by the Clinical Science & Operations Platform (CSO) of Sanofi R&D. The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical activities (clinical part of CTD for registration, feasibility) performed by the CSO. The CSD will provide appropriate medical input and support for all these clinical activities. He/she will provide medical training and medical information to study team(s), Clinical Study Units (CSUs) and investigators. He/she will be deeply involved in the feasibility process. He/she will be accountable for medical review and will collaborate and interact with Pharmacovigilance to review safety data. He/she will interact with Medical Advisors in CRUs or Disease Units), a specialization in a medical area would be requested or at least appreciated. SCOPE: All clinical studies related to projects in clinical development (excluding Clinical & Exploratory Pharmacology studies) and medical investigations (e.g. Registry, survey) for projects in development or for marketed drugs. KEY INDIVIDUAL ACCOUNTABILITIES: • Medical reference and medical expertise for operational strategy within the CSO for study registries he/she is allocated to • Medical consultant for projects to be proposed to the CSO • Medical contact for interaction with physicians responsible for the project or the study at the customer level. • Support with his/her medical knowledge and background a study or a project from • business negotiation with customers to final product delivery (e.g. study completion or • project report or publication) • Conduct the feasibility for study/project with the feasibility manager and other team members (especially Medical Advisors in CSUs) • Prepare and/or organize and/or participate to Investigator's Meetings, Steering Committees, Data Monitoring Committee meetings (only "open” part of the DMC meetings). • Prepare and/or approve any documents related to the study and requiring a medical expertise (extended synopsis, protocol, medical training material for study monitoring team and for investigators) • Provide medical training to study team, CSUs (Medical Advisors, monitoring) and investigators • Develop interaction with Medical Advisors in CSUs for the best knowledge of the study, compound protocol. • Participate to Investigators meetings • Provide medical answers to questions from Health Authorities, IRB/Ethics Committees, investigators, experts • Participate to clinical trial team (and cluster if any) meetings • Accountable for the medical review of data done by the clinical trial team, the case by case review of safety events reported to GPE and coding of events and drugs • Provide appropriate medical input for patient recruitment and retention strategy • Support the CSUs and affiliates to develop network of KOLs and experts and to select National Coordinators or members of Study Committees • Prepare and provide key medical information to investigators and/experts in respect with communication policies (e.g. study results, DMC advice) KEY SHARED ACCOUNTABILITIES: • Feasibility results with feasibility managers • Project/Study deliverables with the Clinical Study Team • Operational strategy with Project Leader (s) • Get support from the Unit Management Office to get appropriate medical staff in CSUs and to determine appropriate study budget according to medical considerations • Collaborate to Adjudication Committee Review including prior patients' data review as needed • Ensure high quality execution from a medical perspective with support of all functions & • Quality & Continuous Improvement group • Ensure appropriate documentation and investigations of safety cases with Global • Pharmacovigilance and Epidemiology (GPE). • Ensure high quality of coding with coding officers Qualifications Basic Qualifications: • Licensed United States Medical Doctor or an International medical graduate who has certification by the Educational Commission for Foreign Medical Graduates (ECFMG). • 2-3 or more years of Phase 2/3 Clinical Research / Drug Development experience in the pharmaceutical industry. Preferred Qualifications: • Knowledge in ICH, GCP and local regulations • Fluent in English (writing and speaking) • Additional Clinical Research and/or Drug Development experience in other therapeutic areas, especially Cardiovascular and Metabolism. Additional Information For more information, Please contact RAKSHAK SINGHAL ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description This role ensures that all components are adequately supplied and kitted to adhere to the production schedule along with handling media related activities within the ISO 8 area. Major Accountabilities ISO 8 Activities: Ensure accurate SAP inventories are maintained for all components. Proper status segregation and storage of media lots. Support the maintenance of an audit ready state of the ISO 8 Area Timely response to all module requests. Batch Records are properly kitted and staged based on production schedule. All gowning materials in the ISO 8 area are maintained to adequate levels. ISO 8 area has ample supply of non-inventory items Logbooks entries are clear and complete. Kanban system is utilized to ensure FIFO Equipment cleaning is performed as required Ensure Batch records are reviewed and corrected in a timely manner. Skills: 1-3 years of related experience in cGMP/FDA regulated industry. Warehouse experience preferred. SAP knowledge preferred. Other Qualifications: Strong interpersonal, written and communication skills along with problem solving and follow-up skills are required. Must be well organized, flexible and work with minimal supervision. Ability to lift up to 50 lbs. Alternate shifts, weekends and overtime will be required Requires handling of chemicals such as corrosives, solvents & bio-hazardous materials Qualifications High School Degree or GED equivalent. Additional Information For more information, Please contact: Akriti Gupta ************** Morristown, NJ 07960

Integration International Inc. is an IT Solutions and Professional Services Company globally HQ in Parsippany, NJ. We offer Application Services, Infrastructure Services and Staff Augmentation Services to Fortune 1000 companies across North America. Our direct Clients are leading names in Banking, Finance, Manufacturing, Publishing, Life Sciences, Technology and Services industry verticals. Please visit us at ************** for more info. Hi, Kindly ignore if this Email is not relevant for you OR have received again. How are you? Hope all is well…. I came across your profile on LinkedIn.com. We have a Wireless Site Survey Assignment in New York, NY; where we need a Wireless Engineer on very urgent basis. Kindly find below mentioned Job description useful and let me know your views upon it as soon as possible. I was trying to reach you to discuss about Managed Deployment Projects & Break-Fix services with our direct client based across New York, USA. We are Urgently looking for Wireless Network Engineers AND Senior Network Engineers having skills/certifications CCIE/CCNP/CCNA AND Wireless Certifications OR having equivalent skill, knowledge, experience as certification is preferred; and who has performed wireless site survey using tool like "Air-Magnet Wi-Fi Analyzer". I was wondering if you would be interested for this assignment. Let me introduce you to our company: Integration International Inc. is an IT Solutions and Professional Services Company globally HQ in Parsippany, NJ. We offer Application Services, Infrastructure Services and Staff Augmentation Services to Fortune 1000 companies across North America. Our direct Clients are leading names in Banking, Finance, Manufacturing, Publishing, Life Sciences, Technology and Services industry verticals. Please visit us at ************** for more info. Hours and Date of operation: Week of 13th June 2016 Required Resources: • 1 CCIE OR Senior Equivalent Engineer & 1 CCNP OR Junior Equivalent Engineer. • 4 - 6+ years of experiences in networking. • Communication skills: English Assignment Details (Wireless) Information Need to Capture in Wireless survey • Physical locations of access points • Recommended access point power and channel settings • Antenna type, location, and orientation specifications • Power, mounting, and cabling specifications • Any known or measured sources of interference • Document gaps between requirements and the existing RF design and make recommendations for improvement to address coverage, interference, and contention issues • Real-time data rate of associated client • Packet loss • Retransmission • Actual client behavior • More Accurate AP placement location • Link Speed. Deliverables required From Engineer for Wireless Assignment: • Custom RF design. • WLAN GAP Analysis and Audit • Spectrum Analysis report • Audit Existing Wireless Infrastructure: • Capture HD quality pictures complete site Below are the Roles & Responsibility: • An individual who can perform the Wireless Site Survey for Data and Voice across all the buildings and floors. Provide recommendation on Access-point placement map, Signal-to-noise ratio map, any potential interference map. • Experience working on Wireless Tools like Cisco Prime, Air Magnet, worked on RF Design. • Review requirements for the wireless LAN RF design, including required signal strength, signal to noise ratio (SNR) design levels, data rates, throughput, availability and capacity. • Perform onsite verification. • Inspect, measure and document the physical plan and wireless network • Identify facility structures and communication devices that might interfere with radio signals or placement of wireless transmitters and access points. • Scan for significant wireless LAN networks or major sources of non-802.11 interference • Test propagation characteristics, coverage area, and signal quality Tools Required for the Wireless Assignment: • Wi-Fi Analyzer Software/Hardware, Laptop, Console Cable Kindly reply to this email with below requested information. 1. Do you hold any wireless certification, if yes please specify? 2. Have you performed wireless survey in past? 3. Experience on performing Active Survey? 4. Do you have software/hardware to perform wireless survey? (Air Magnet/ Ekahau) If yes, please confirm the name? 5. Do you have RF Spectrum Analyzer 2.4GHz & 5GHz? 6. Do you have WAPAP 3702 I/E and 2602I/E with power adapter and 3 - 5 meter Cat 5/6 cable? 7. Do you have Tripod Stand for Wireless Access Points (if available at client site, will let you know; but tell me if you have it) 8. Do you have Camera to capture pictures to use those pics as reference while creating the survey report 9. Do you have Internet Dongle 10. Any experience working on Analyzer and providing report? 11. Do reply with copy of updated resume. Please share your most updated resume having wireless experience on it. As per feedback from SA, they want to see any prior wireless experience, tools (SW/HW) utilized for wireless activity need to reflect on the resume. Also share your wireless survey report sample preformed earlier. 12. Expected hourly pay rate in USD currency all inclusive? 13. Please specify your best time to have a Telephonic Discussion with our Solution Architect along with your Cellphone Number? Pay Rate: Please confirm your hourly pay rate in USD currency all inclusive. Pay Term: It will be monthly invoicing. Your first invoice will be paid on 15th day once the month is completed. And 2nd invoice onwards it will be Net 45 days' Pay Transfer to your PayPal account. Pay Process: PayPal Also, As per Latest Client Update, we need below mentioned information to be filled by the Engineer for the Respective Assignment. Kindly provide us with the estimated hours you need for the Each phase of This Assignment. Site Sq. Footage Onsite Survey (Hours) Documentation (hours) Customer Meetings (Hours) Final Report Submission (Hours) Remediation + Optimization + Revision in Report (Hours) Not to Exceed Total Hours 2700 sq. ft. Kindly confirm above mentioned points, Would look forward for your quick response. Qualifications CCIE Wireless OR CCNP Wireless OR CCNA Wireless Additional Information All your information will be kept confidential according to EEO guidelines.