Scientist II- Whitesboro, New York- Full-Time; Onsite ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. The Role: We are looking for a Scientist l to join our winning laboratory team rated by Forbes as one of America's best employers for two years in a row! Must be flexible and available for self-paced training Monday thru Friday and able to work occasional weekends. • Under general supervision, the Scientist in the bioanalytical laboratory will be responsible for developing and performing assays on biological samples from pre-clinical and clinical trials. • The Scientist will validate the quantification of Biomarkers, New Chemical and Biological Entities in tissues, biological fluids or chemical matrices. • Perform assays for routine batch analysis of Biomarkers, NCE and NBE in biological fluids/chemical matrix involving simple to complex analytical techniques. • Perform laboratory work to FDA and international regulatory GLP and GCP standards. What you need: We are seeking candidates with a Bachelors in Biology, Chemistry, or Biotechnology and the ability to work in a fast paced collaborative environment. Familiarization with basic laboratory operations is preferred. Knowledge of binding assay formats and platforms, effective communication skills, attention to detail, and the ability to organize and prioritize work is required. Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
* Various annual leave entitlements
* A range of health insurance offerings to suit you and your family's needs.
* Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
* Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
* Life assurance
* Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Salary range: $56,704.00-$70,880.00
Bonus, Com, Stock, Benefits & Disclaimer verbiage:
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.
Are you a current ICON Employee? Please click here to apply
$56.7k-70.9k yearly 2d ago
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Project Manager I EDS
Icon Plc 4.8
Icon Plc job in New York, NY
Project Manager I EDS - US, Whitesboro NY, Whitesboro Hybrid: Office/Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Project Manager I EDS to join our diverse and dynamic team.
What You Will Be Doing:
* Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.
* As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
* Travel (approximately 1%) domestic and/or international.
* Monitor and evaluate bioanalytical projects progress with respect to milestones, budgets and timelines.
* Manage bioanalytical studies to ensure that bioanalysis is well coordinated with in life study phases, and that samples are appropriately tracked throughout the lifetime of the study and any agreed storage period.
* Work with laboratory management to ensure that appropriate resources are available to complete the study to timeline.
* Obtain all client specific documents required for the analysis; i.e., study protocol, randomization lists, COA, demographics, etc. Review protocol and amendments to assure adherence to specifications and regulatory requirements.
* Prepare analysis plans suitable to the client's needs, as specified by contract, and obtain client approval of these.
* Work with laboratory operations to ensure compliance to study and validation plans.
* Provide Sponsors with regular updates, forecasting and communicating study progress. Timely reporting of any significant deviations.
* Ensure that project delivery, reporting specifics, and timelines as agreed are met. Inform laboratory operations, DM and QC/QA of deadlines.
* Maintain records of work conducted in a timely and consistent manner, sufficient to allow real-time tracking of deliverables, including tracking of revenue and resources associated with assigned studies.
* Identify changes to scope of work as defined by contract and ensure that change orders are processed prior to work being executed.
* Review and approve all data in accordance with direction documents and ensure results are documented accurately, completely and compliant with GxP regulations and SOPs. Initiate investigations and event deviations as necessary.
* Proactively identify possible/potential implications of unusual results, work with laboratory staff to investigate and report findings.
* Prepare reports of the work conducted, address all QA findings and provide QA draft report in line with the terms and conditions stated in the signed contract.
* Ensure that all documentation is appropriately archived on completion of the study.
* Review and approve laboratory notebooks and other analytical data as required.
* Maintain awareness of and adherence to all current SOPs.
* Work in compliance with GLP/GCP.
* Any other duties related to maintaining the provision of the Laboratory Analytical Services.
Your Profile:
* A suggested minimum of 3 years' experience in a laboratory or project management role, at discretion of hiring manager.
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
* Various annual leave entitlements
* A range of health insurance offerings to suit you and your family's needs.
* Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
* Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
* Life assurance
* Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Salary range: $68,616.00-$85,770.00
Bonus, Com, Stock, Benefits & Disclaimer verbiage:
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.
Are you a current ICON Employee? Please click here to apply
$68.6k-85.8k yearly 7d ago
Automation Expert - Selenium Java
Integrated Resources 4.5
New York, NY job
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.
• Primary Skill: Selenium with Java
• Top 3-5 skills & min. year experience required for each:
• •At least 5 years' experience in Test Automation Strategy and planning creation and implementation
• Good Knowledge knowledge in keyword , custom Selenium framework or data driven framework
• At least 2 year experience in hands-on scripting automation experience using Selenium with Java as programming Language
• Good knowledge on Java Programming with 2 years of programming experience
• Provide a job description of the role, responsibilities and qualifications required for this position: Automate Web automation to run on multiple browsers and develop / design the automation framework. Work with development to understand the design and raise any automation road blocks.
• Provide a list of optional skills: Manual Testing
Qualifications
• Overall Exp: 5 to 8 years
If you are not interested in looking at new opportunities at this time I fully understand. I would in that case be appreciative of any referrals you could provide from your network of friends and colleagues in the industry. We do offer a referral bonus that I'd be happy to extend to you if they turn out to be a great fit for my client.
Thank you for your time and for consideration. I look forward to hearing from you.
Additional Information
Kind Regards
Sachin Gaikwad
Technical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
Direct Line : 732-429-1920 Ext 301
Board: 732-549-2030
LinkedIn: www.linkedin.com/in/gaikwadsachin
Gold Seal JCAHO Certified ™ for Health Care Staffing
“INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)
$100k-169k yearly est. 60d+ ago
ETL Architect
Integrated Resources 4.5
New York, NY job
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
$102k-130k yearly est. 60d+ ago
Recruiter Level 3
Integrated Resources 4.5
Jersey City, NJ job
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.
This position is with my direct client
Request: Recruiter Level 3
City: Newark
State/Province: New Jersey
Duration: Duration: 6 Months (Temp to perm)
• Minimum of 5-10 years corporate recruiting experience required
• Experience recruiting for Marketing/Underwriting positions
• Temp-perm opportunity
• Bachelor's Degree required
Job Description:
This position serves as a strategic recruiting partner to the business units, and is responsible for attracting, identifying, interviewing, selecting and converting top talent for highly specialized and Director level positions. Provides mentorship and guidance to other recruitment staff.
- Initiate & maintain consultative, strategic partnerships with Directors and Hiring Managers to understand their talent acquisition needs to fulfill business objectives.
- Analyze position requirements and develop recruiting plans using innovative strategies to attract high caliber talent.
- Screen resumes, conduct phone interviews and evaluate candidates' job qualifications. Present hiring managers with selection qualified candidates. Develop and implement behavioral based interview techniques to assess candidates' competencies and make hiring recommendations.
- Manage candidates' expectations throughout the entire recruitment process; provide information regarding compensation, benefits, company history, career paths and policies, and promote a positive image
- Determine appropriate salaries; negotiate and close offers with selected candidates, and initiate on-boarding process. Follow up and maintain communication with key candidates not selected.
- Ensure that recruitment strategies support the enterprise diversity initiative and drive performance metrics (quality of hire, time-to-fill, cost of hire, customer satisfaction, etc). Maintain accurate records for OFCCP and EEO compliance, and complete various reports on recruiting metrics.
- Serve as subject matter expert and consultant to business areas. Provide education on labor market trends, interviewing techniques, recruitment processes, etc.
- Apply industry knowledge and best practices to make continuous improvements to the recruiting processes and standard operating procedures.
- Oversee work of clerical staff.
Education/Experience:
- 6+ years of full-cycle recruiting experience. Combination of search firm and corporate experience preferred.
- Experience conducting high-level searches
- Bachelor's degree or 2 year degree plus relevant work experience required
Knowledge:
- Knowledge of sourcing methodologies, including searching/posting on job-boards.
- Demonstrated knowledge of candidate attraction, behavioral-based interviewing, selection and closing techniques.
- Familiarity with candidate contact databases
- Proficiency with Microsoft Office Suite.
Skills and Abilities:
- Superior written, oral and interpersonal communication skills.
- Excellent listening skills.
- Strong customer service orientation.
- Ability to be creative and resourceful.
- Ability to handle multiple priorities in a fast-paced environment.
- Ability to interface at all levels throughout the organization.
Travel (If Applicable):
- May require travel to other NJ office locations
Qualifications
Bachelors
Additional Information
Regards
Harshad
732-429-1922
$60k-84k yearly est. 60d+ ago
Project Coordinator
Integrated Resources 4.5
Jersey City, NJ job
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
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
$45k-64k yearly est. 60d+ ago
Survey Technician
Integrated Resources 4.5
Newark, NJ job
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
Prepare site and subdivision plans using MicroStation CAD software.
Development and maintenance of various corporate spatial datasets.
Prepare reports, graphic and tabular, using Micro station CAD software tools for analysis.
Qualifications
Minimum 5 years direct experience performing land surveying calculations.
Preparing boundaries and site plans using MicroStation CAD and COGO programs.
Writing metes and bounds descriptions.
Additional Information
Regards,
Monil Patel
Technical Recruiter
Integrated Resources, Inc
(732) 844-8747 Ext.338
monil @irionline.com
$55k-74k yearly est. 60d+ ago
Drug Safety Coordinator
Integrated Resources 4.5
Florham Park, NJ job
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
$53k-81k yearly est. 60d+ ago
Performance Measurement Lead
Integrated Resources 4.5
Newark, NJ job
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
- Soft Skills: detailed oriented, tactical mindset, polished, can communicate effectively with director level and above
- Main Functions: Prepare scorecard decks for all organizations at PSEG, support with bench marking, develop business improvement strategies
- Must have some knowledge of the utility business
- Must have knowledge of Excel, Access, Tableau
- Responsible for some data entry
- 3 to 5 years in analytics
Qualifications
Required:
• BA or BS Degree or equivalent experience.
• Demonstrated organization and high level of analytical and quantitative skills. Must have extensive proven proficiency with MS Office Products, Excel, Access, Word and PowerPoint.
• Demonstrated ability to develop new approaches with applicable tools to measure success. Demonstrated detail orientation and ability to work independently. Demonstrated ability to work across department boundaries.
• Must foster an inclusive work environment and respects all aspects of diversity.
• Must demonstrate and value differences in others' strengths, perspectives, approaches, and personal choices.
• Must have a driver's license
Additional Information
Regards,
Nagesh
Sr.Technical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
Direct# 732-429-1641
(BOARD) # 732-549-2030 - Ext - 305
LinkedIn: https://www.linkedin.com/in/nageshghanti
Gold Seal JCAHO Certified ™ for Health Care Staffing
“INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)
$96k-125k yearly est. 60d+ ago
Associate Director, Medical Writing - Neuroscience
Integrated Resources 4.5
Woodcliff Lake, NJ job
The Associate Director - Medical Writing will be the designated Lead Medical Writer for approximately 3 Neuroscience or General Medicine Programs, responsible for providing needed support and direction to other staff/contractors on these programs. As the lead writer, the incumbent ensures timely completion, accuracy and quality of all clinical and submission documentation across all aspects of the compounds' life cycle management. Due to the complexity of the programs, the incumbent must rapidly acquire complete and advanced knowledge of the compound to ensure alignment and consistency across studies. The qualified candidate will have proven ability to effectively manage the outsourcing of document preparation when necessary and the associated service providers.
Responsibilities include but are not limited to:
Working on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors
Independently prepares and at times may direct, the writing of PCSs, protocols and protocol amendments
Independently prepares and at times may direct, all the writing of the CSRs including narratives
Works across functional areas to obtain all applicable source materials
Leads the preparation of clinical sections of submission documents, such as the briefing books, Global Investigator Brochures, and annual regulatory reports
Leads the medical writing activities for marketing application submission documents
Liaises with other functional areas and groups in the development of document standards and structure
Interacts routinely with clinical research and biostatistics staff to gain comprehensive understanding of the study design, and results across the program
Implements document quality controls, standards and best practices
Qualifications
Job Qualifications
BS required/MS preferred
Minimum of 8 years medical writing experience in an industry setting, with specific experience with compounds in Neuroscience
Must have participated in or lead a major marketing application submission
Strong critical thinking and problem solving skills
Self-motivated with the ability to influence others
Ability to multitask on complex projects
Result driven with a mastery of time management and project planning
Able to work on site
Advanced working knowledge of MS project and MS Word
Experienced in the use of a documentum system
Additional Information
All your information will be kept confidential according to EEO guidelines.
$125k-235k yearly est. 60d+ ago
Controls/Substation Designer
Integrated Resources 4.5
Newark, NJ job
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: Controls/Substation Designer
Duration: 2 years, possible extension to 4 years
Location: 80 Park Pl. Newark, NJ
Direct Client: Immediate interview
Description: At least 3 years' experience working completely independent on controls/protection design for electric utilities' 26kV up to 500kV switching stations and substations projects for new stations or modifications of existing stations starting form one line control, tripping table, schematics up to point to point wirings, rack arrangements, etc.
Working knowledge of Micro station &AutoCAD.
These requirements are a must and if the candidate does not have exactly this experience he cannot be considered for this position.
Responsible for providing project design of the controls discipline for electrical utility controls projects for high and middle voltages Switching stations and Substations (13, 26, 138, 230 & 500kV).
Provide technical expertise to the Divisions and construction.
Check field conditions on the assigned projects.
Proficient in working on the following Controls drawing documentation based on the scope of work:
One line diagrams, relay protection and control schematics, instrumentation and alarm schematics, SCADA controls, racks and panels front views, wiring diagrams, equipment layouts and cable schedules, bill of material.
Working with vendor and manufacturer documents.
Working with Electrical, Civil designers and engineers, System protection, construction supervisors and field personnel.
Position required emergency response to fail equipment restoration.
The candidate must possess the following:
BS in electrical engineering, experience in electrical utility project controls design engineering with at least 3 years' experience of working on moderate to large projects.
Shall work with minimum of supervision and be a good team player.
Take personal accountability of actions and results.
Focus on a project completion on time.
Computer skills: MS Office (Word, Excel), Micro station, AutoCAD.
Additional Information
Thank You
Nagesh
732-429-1641
$77k-107k yearly est. 60d+ ago
Business Operations Associate
Integrated Resources 4.5
Florham Park, NJ job
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
• Procurement and Budget Tracking.
• Prepare and process all purchase orders, invoices, and other payments (within 72 hours of receipts) and reconcile departmental expenses when problems arise (initiate request for resolutions with 72 hours of identification).
• Maintain tracking system for all payments that flow though the U.S.
• Obtain actual and prepare spending reports (after the close of each accounting periods as requested by manager for global group).
• Work within Finance on monthly expenses and departmental budget forecasting & tracking. Contract Management
• Maintain FCPA compliance with agreement's and initiate follow-up actions as needed.
• Coordinate the compilation, distribution and storage of all departmental legal agreements and related U.S.-routed documents utilizing Ariba contracts and update all (global) post-agreement records via tracking documents and POMS.
• Coordinate the entry of all CDAS agreements into Ariba contracts, POMS, and our master agreement list. Supply information for agreement audits as needed. Information Systems and Reporting
• Enter unsolicited opportunities into POMS.
• Management of the partnering inbox from our website to assign “New Submissions” reminding opportunity owners that submissions (15 days and older) need to be progressed into Initial Review. Upload and maintain new content within departmental SharePoint site.
• Maintain monthly and High Priority BD Report (Business Development). Operations and Administrative Performing various administrative functions under minimal supervision for CDAS - US/Florham Park based colleagues. Calendar management through Outlook; Arranging various meetings; corresponding with other team members within the group; assisting with all aspects of meeting planning and special events including offsite full team meetings, reserving conference rooms; assisting with meeting materials i.e. agendas, presentations, pre-read materials; binders and other necessary documentation - in a timely manner.
• Making travel arrangements including air, hotel and ground transportation; developing travel itineraries. Expense Reports: Prepare and maintain expense reports in a timely basis through expense reporting system; must have ability to take the initiative in solving problems independently.
• Legal documents: Independently sort and distribute incoming materials and distribute key documents to appropriate team members for signature and filing.
• Back-Up Support: Provide support directly to Senior Vice President in Executive Assistant's absence.
KEY CRITERIA: Finance Background. Data Systems Management. Experience with Contract Management & Compliance. Managing Global Budgets. Ability to track capital and expense projects.
SKILLS: SharePoint, Microsoft Word, Excel, PowerPoint, Outlook, SAP. Experience with numerous computer system programs.
Qualifications
Bachelor's Degree
Additional Information
Contact - Kashish Vermani 732-429-1912
$62k-94k yearly est. 3d ago
Microbiologist
Integrated Resources 4.5
Newark, NJ job
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
$57k-79k yearly est. 60d+ ago
Laboratory Assistant
Icon Plc 4.8
Icon Plc job in New York, NY
Laboratory Assistant- Whitesboro, New York- Onsite, FULL-TIME ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Laboratory Assistant to join our diverse and dynamic team. As a Laboratory Assistant at ICON, you will provide essential support to laboratory operations by assisting with the preparation, organization, and maintenance of laboratory samples and equipment. Your role will be crucial in ensuring a smooth workflow and contributing to the accuracy and integrity of laboratory results.
What You Will Be Doing:
* Assisting with the preparation of laboratory samples and reagents according to established protocols and procedures.
* Maintaining laboratory equipment and supplies, ensuring cleanliness and proper functioning at all times.
* Documenting and tracking sample information, including labeling, storage, and retrieval of samples as needed.
* Supporting laboratory staff in conducting tests and analyses by providing timely assistance and preparation of materials.
* Participating in maintaining a safe and compliant laboratory environment, following all safety protocols and guidelines.
Your Profile:
* High school diploma or equivalent; associate degree in a relevant field preferred.
* 0-2 years of experience in a laboratory or related environment, with a strong willingness to learn and develop new skills.
* Strong attention to detail and organizational skills, with the ability to handle multiple tasks efficiently.
* Good communication and teamwork abilities, with a proactive approach to supporting laboratory operations.
* Basic familiarity with laboratory equipment and techniques is a plus.
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
* Various annual leave entitlements
* A range of health insurance offerings to suit you and your family's needs.
* Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
* Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
* Life assurance
* Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Salary range: $35,208.00-$44,010.00
Bonus, Com, Stock, Benefits & Disclaimer verbiage:
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.
Are you a current ICON Employee? Please click here to apply
$35.2k-44k yearly 8d ago
Senior Bio statistician
Integrated Resources 4.5
Woodcliff Lake, NJ job
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
Client: Direct Client
Location: Woodcliff Lake, NJ
Job Title: Senior Biostatistician
Duration: 12 Months to 36 (Possible Extension)
Summary:
• Work closely with clinicians, programmers, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review.
• Work with the clinical study team on study design, development and/or review of clinical study protocols.
• Develop and/or review statistical analysis plans, including Table/listing/figure shells, and final study report for clinical studies; perform post-hoc statistical analyses as needed.
• Work with the project statistician and clinical data managers on design/review of case report form, data transfer specification, edit check specification, and participation in user acceptance testing (UAT); generate/review data tables/listings and coordinate data review meetings during the course of the study to ensure data quality.
• Oversee CRO programming activities, perform quality assurance checks on internally or externally produced SAS tables, listings, and figures, and ensure the quality of CRO deliverables.
• May work with the Health Outcome team on the design/analysis/validation of projects.
• May work on submission teams as a statistician and/or a programmer.
• Act as lead Statistician on complex trials and across multiple studies.
• Act as a lead representative of the of the biostatistics department on project teams.
Feel free to forward my email to your friends/colleagues who might be available
Qualifications
Education & Experience:
• Must have a MS in Biostatistics/Statistics with at least 10-12 years of experience or a PhD in Biostatistics/ Statistics with at least 6 years of experience in the pharmaceutical, CRO or biotech industry.
• Strong SAS programming skills. - At least 3-5 years.
• Oncology experience is highly preferred.
• Good technical writing skills.
• Good communication skills (verbal and written).
• Strong teamwork ability/commitment and individual initiative.
• Strong organizational skills with ability to effectively manage multiple projects.
• We need is an experienced statistician who can do SAS programming at the same time can clearly interpret statistical concept and results to non-statisticians and key medical opinion leaders
Additional Information
Warm Regards,
Jay Kaushik
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
(Direct) 732-429-1633 | (W) 732-549-2030 x 211 | (F) 732-549-5549
Linkedin: https://www.linkedin.com/in/jay-kaushik-a992a6a9?trk=hp-identity-name
Visit to our Website: www.irionline.com
Gold Seal JCAHO Certified ™ for Health Care Staffing
“INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)
$85k-127k yearly est. 60d+ ago
Sr. Regulatory Affairs Specialist
Integrated Resources 4.5
Edison, NJ job
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.
This is a Direct Hire role with the client
Job Description
**WORK LOCATION IS DAYTON,NJ**
JOB SUMMARY
This will person will be a Regulatory liaison between product development and the regulatory agencies. This position will be responsible for regulatory submissions for new ANDAs and any changes being made to existing products. The position will also assist in labeling for new products, changes to labeling for existing prescription and OTC products. This position will also interact with other departments and cross functional teams both in US and India.
REPORTING RELATIONSHIPS
Depending on the experience of the candidate, one labeling associate may report to this position.
DUTIES & ESSENTIAL JOB FUNCTIONS
• Regulatory support of new and existing products including the preparation of ANDAs, supplements, Annual Reports, and responses to FDA deficiency letters/information requests.
• Independently manage preparation (in paper or electronic formats (eCTD and SPL)), submission and monitoring progress of FDA review of ANDA's
• Communication with functional groups for coordination and preparation of data for submission to FDA
• Manage all Regulatory, Federal and State License requirements
• Review change controls for regulatory requirements and according to appropriate regulations and guidance's.
• Familiar with Regulatory regulations (e.g. FDA guidance, ICH, 21 CFR etc)
• Review labels as per FDA guidance
• Regulatory support in drug listing.
• Perform other duties as assigned
**WORK LOCATION IS DAYTON,NJ**
Qualifications
**WORK LOCATION IS DAYTON,NJ**
QUALIFICATIONS
• BS or MS degree in a scientific discipline, preferably Chemistry, Biology or Pharmacy
• 1 - 2 years' experience in pharmaceutical regulatory affairs (mandatory)
• Attention to detail
• Excellent oral and written communication skills
• Knowledge of US drug regulatory requirements (mandatory)
REQUIRED
BS or MS in Sciences or Pharmacy
PREFERRED
Experience with eCTD filings
Regulatory Affairs Certification (RAC)
**WORK LOCATION IS DAYTON, NJ**
Additional Information
$71k-102k yearly est. 60d+ ago
Clinical Research Scientist
Integrated Resources 4.5
Woodcliff Lake, NJ job
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
Title: Clinical Research
Scientist
Duration: 12 Months (Possibility of Extension)
Location Woodcliff lake NJ
Job Responsibilities:
The incumbent is responsible for, but not limited to the following:
Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies
Prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, ISE, Investigator Brochure, etc)
Performs literature search and data analysis to address research questions
In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct (enrollment, GCP practices, handling of safety issues, etc.)
Assisting in database cleaning, review of study results, and interpretation of results
Adhering to key performance indicators for clinical study development, conduct, and reporting
Individual contributor with specialized knowledge
Presents concepts, facts, and reports and advises on key trends and issues
Troubleshooting routine site inquiries
Work is completed under limited supervision
Supports the planning, execution and reporting of clinical programs/trials
May handle multiple protocols simultaneously
Contributes to risk resolution by escalating and monitoring project risks
Qualifications
Qualifications
Minimum of
2-5 years of experience in clinical research in the pharmaceutical industry
A thorough understanding of clinical research methodology including study design, protocol writing, and CRF preparation is required, as is a knowledge of GCP and local regulatory requirements
Working knowledge of the IND/NDA/CTD/MAA process acquired through direct industrial experience preferred
Knowledge of medical, scientific and clinical research techniques in the oncology therapeutic area;
Bachelor's Required. Doctoral (PharmD or PhD) or MD degree preferred
.
Additional Information
Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus
Thank you for your time and consideration. I look forward to hearing from you!
Kind Regards
Ruchi Kumari
Clinical Recruiter
Integrated Resources
, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE
|
GSA - Schedule 66
I
GSA - Schedule 621I
(DIRECT BOARD) #
732-844-8716
(F) 732-549-5549
LinkedIn:
https://www.linkedin.com/in/ruchi-kumari
Gold Seal JCAHO Certified ™
for Health Care Staffing
“INC
5
0
0
0
's
FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)
$77k-115k yearly est. 3d ago
QC Chemist- Protein Experience
Integrated Resources 4.5
Edison, NJ job
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.
Our client is a public and rapidly growing diagnostics company that is looking to expand their Quality team in Memphis TN. They are willing to assist with relocation. This position will have 4 direct reports. Relocation assistance is provided! Excellent benefits, competitive salary, and stock options.
Job Description
Protein Chemistry Background required
NO Ph.d please. Must have previous supervisory role.
Duties and Responsibilities.
Perform QC chemistry testing for research and clinical batches.
Perform stability testing for research and clinical batches.
Execute method validation activities in support of the departmental strategic plan
Support Quality Assurance programs / initiatives as necessary
Perform and/or coordinate raw materials testing
Pull and perform testing in a timely manner
Report results in a timely manner (e.g., database; logbook)
Performing work in accordance with Good Manufacturing Practices and Quality System
Other items as deemed necessary by management
Qualifications
Graduate Degree and a Protein Chemistry background is required
Additional InformationAll your information will be kept confidential according to EEO guidelines.
$61k-79k yearly est. 60d+ ago
Quality Systems Director
Integrated Resources 4.5
Edison, NJ job
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 Director of Quality Systems is responsible for the Quality System as they relate to Investigations, Training and Auditing of suppliers and third party manufacturers. The Director must have sufficient experience in manufacturing pharmaceutical products and understand industry standards to appropriately evaluate practices and procedures and be very familiar with various types of manufacturing technologies including oral solid dose, oral liquid, topical and sterile pharmaceutical products. The experience should include specific technologies such as wet granulation, fluid bed coating, high speed compression, encapsulation, tablet coating, and sterilization techniques such as steam, dry heat, filtration, Ethylene Oxide and Gamma Irradiation. The qualified candidate has appropriate experience in dealing with Governmental officials within the FDA at the District and Center levels. Additional areas of responsibility include evaluating staffing needs, establishing requirements as per GMP and European standards, budget, training, prioritizing and scheduling of team activities and reporting quality progress on a weekly basis to site management. This position must assure all GMP systems are of the highest quality and meet all applicable standards.
ESSENTIAL JOB RESULTS
· Responsible for implementing and maintaining a compliant Quality System per FDA and ISO requirements
· Oversee these quality systems within Novel: manufacturing, GMP documentation, quality records management, Validation, change control, calibration, labeling & packaging, product assessment and disposition, warehouse and distribution.
· Provides assurance that SOPs and practices within the manufacturing, testing, holding and distribution areas are adhered to and are appropriately maintained
· Responsible for assuring compliance of products manufactured in Novel's plant in Somerset.
· Assure GMP requirements are met and appropriate documentation is maintained
· Promote organization's growth and adherence to industry standards
· Ensures all company procedures, policies and systems are in accordance to industry regulations.
· Direct the development and implementation of departmental goals and objectives.
· Reporting on the performance of the quality system to corporate representatives and internal management.
· Coordinates, prepares, participates & responds to FDA, Foreign regulatory agencies and third party inspections.
REQUIRMENTS
Education
Minimum Bachelor Degree in a scientific or technical field; graduate degree desired.
Experience:
· 9+ years' experience in a Quality and/or Regulatory management position in pharmaceutical manufacturing, preferably with some experience in aseptic processing.
· Working knowledge of FDA and applicable non-US regulations pertaining to pharmaceutical drug manufacturing
· Excellent managerial skills; includes project management, problem-solving, written and verbal communications, and organizational abilities
· Excellent teamwork, leadership, influencing, and coordinative skills; must be able to work with diverse teams to achieve results
· The ability to train employees, develop junior managers, and raise process improvement skills and overall quality standards across multiple functions
Qualifications
Additional InformationAll your information will be kept confidential according to EEO guidelines.
$120k-169k yearly est. 60d+ ago
Network Security Analyst
Integrated Resources 4.5
Newark, NJ job
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