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A Truck Driving job is waiting for you. Earn your Class A CDL today!
CRST Expedited - Woodbridge, NJ
Mar 22, 2017
CRST Expedited is hiring Class A CDL truck driver trainees. We will teach you how to keep your CDL Class A truck driving license clean...
CRST Expedited is hiring Class A CDL truck driver trainees. We will teach you how to keep your CDL Class A truck driving license clean with proper training. Apply for a CDL-A student truck driving job today! We offer no-cost CDL-A training and free room & board while you're at our academy and, in return, we'll ask you to drive for us for ten months. It's not the plaza hotel, we wish it could be, but it's clean, safe, and a way to get you trained and earning quickly. Thousands of successful drivers have come through our driving academy and gone on to earn well over $100k per year. That's not a typo.
Food Service Workers - Become a Lyft Driver
Lyft - New York, NY
Mar 24, 2017
Make up to $1500/week driving for Lyft. What is Lyft? Lyft matches drivers with passengers who request rides through our smartphone...
Make up to $1500/week driving for Lyft. What is Lyft? Lyft matches drivers with passengers who request rides through our smartphone app, and passengers pay automatically through the app. Signing up to be a Lyft driver is the perfect opportunity for you to earn extra cash – whether you’re trying to offset costs of your car, cover this month’s bills, or fund your dreams. Why Lyft? Keep Your Tips - Earn Tips from your passengers and keep the whole amount - they're yours Make More Money - With increased Prime Time pricing during peak hours, you make more with Lyft Best Community - The Lyft community is full of awesome, friendly people. How Lyft Driving Works Open the app and turn on driver mode Accept a ride request Pick up your passenger Once the ride ends, the app processes pay from the passenger's saved credit card Lyft provides additional insurance policies, at no cost to the driver. We worked with leading insurance carriers to get our drivers: commercial auto liability insurance up to $1M per occurrence, contingent collision insurance for drivers who carry collision coverage on their personal auto policy, and coverage for bodily injury caused by uninsured/underinsured motorists. If you already carry commercial insurance or personal coverage providing specific coverage for ridesharing, Lyft’s policy will continue to be excess to your insurance coverage. Please note, the above coverage may be modified to comply with local regulations or state laws. Lyft’s policy is not available in New York State at this time. Passenger Ratings Drivers rate passengers after each ride, so you’ve always got a say. We also require passengers to provide valid credit card information for identity verification purposes. Lyft is Everywhere Lyft is available in over 60 cities in the US and launching in new cities every week! What are Lyft’s requirements? You must be at least 21 and own an iPhone or Android phone. As part of our approval process, you’ll undergo a DMV check, plus a national and county background check. This will require a Social Security number, in addition to an in-state driver’s license that is at least a year old. Learn more about our background check standards on our Safety page, and our comprehensive driver requirements in the Help Center. Your car needs to have four external door handles and at least five total seat belts. You must be a covered party on your car’s in-state insurance, and have in-state license plates. We’ll confirm all of this during your 19-point vehicle inspection. Cars have Lyft age requirements too, which can vary by state. See your state-specific requirements.
IT Project Managers - Healthcare Payer Consulting (MN, NJ, or IL)
UnitedHealth Group - Basking Ridge, NJ
Mar 24, 2017
What can YOU do with the right information? At OptumInsight, the possibilities and the impact are limitless. You'll be empowered to ask...
What can YOU do with the right information? At OptumInsight, the possibilities and the impact are limitless. You'll be empowered to ask more questions, develop better solutions and help make the health care system greater than ever. It's always fresh. It's always exciting. As an IT Project Manager, Healthcare Payer Consulting you'll provide people, process and technology consulting services to strengthen and improve health care operations that result in stronger financial returns and a healthier health care system. You'll use your strong strategic and business acumen to work closely with clients to define, develop and document business requirements to ensure needs are captured and critical deliveries are executed. This consulting career gives you the opportunity to travel and share in a mission that inspires. You'll see your ideas come to life and your achievements recognized. You won’t find more interesting challenges. And you won’t find smarter people working together to solve them. Join us and start doing your life's best work.(sm) Travel is required for this role. Our consultants typically travel Monday through Thursday but could leave on Sunday and return on Friday. Consultants work from a home office when not at the client site. Primary Responsibilities:Collaborate with business and technology departments to define deliverables and develop solutions that are reusable across the organization Conduct research studies that may include collecting, analyzing, trending and presenting data and recommendations to management Perform project / program management duties including the creation of status reports, work plans, and presentations to client leadership Identify and document business process re-engineering opportunities including current and future state process flows Identify opportunities for client account growth and perform a leadership role in conjunction with the sales leaders to close add-on business Define, develop and document business requirements to ensure clients' needs are captured and delivered Participate in quality assurance and user acceptance testing by writing test scripts, executing test cases and documenting defects Develop financial models and tools, including cost-benefit analysis, resource utilization models and performance reports Produce job aids, training material and instruction manuals for end-usersRequired Qualifications:5+ years of working in a Management Consulting/Professional Consulting organization 3+ years of a combination of experience from : IT Consulting, Finance/Banking, Pharmaceutical/Life Sciences, Engineering, Strategy, and/or Biotech 5+ years of experience in any of the following areas: Business Analysis, Systems Analysis, Project / Program Management, and/or Business Process Improvement 4+ years of experience with software applications Systems Development Life-Cycle (SDLC), agile methodology, database management systems, and other business-related technologies 4+ years of building/creating project / program deliverables with the ability to manage 3+ complex work streams 4+ years demonstrated experience in a client account growth and relationship expansion 5+ years of client-facing experience Ability to travel up to 80% Candidates must be able to work in one of the main hub locations such as: Minnetonka or Eden Prairie, MN or Basking Ridge, NJ or Chicago, IL Preferred Qualifications:Bachelor's Degree Healthcare experience (with strong preference given to Payer experience) Strong communication (written and oral), interpersonal, team, and conflict resolution skills Experience with project turnaround/remediation Strong communication (written and oral) and interpersonal skills Ability to leverage professional networkCareers with Optum. Here's the idea. We built an entire organization around one giant objective; make health care work better for everyone. So when it comes to how we use the world's large accumulation of health-related information, or guide health and lifestyle choices or manage pharmacy benefits for millions, our first goal is to leap beyond the status quo and uncover new ways to serve. Optum, part of the UnitedHealth Group family of businesses, brings together some of the greatest minds and most advanced ideas on where health care has to go in order to reach its fullest potential. For you, that means working on high performance teams against sophisticated challenges that matter. Optum, incredible ideas in one incredible company and a singular opportunity to do your life's best work.(sm) Diversity creates a healthier atmosphere: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, protected veteran status, disability status, sexual orientation, gender identity or expression, marital status, genetic information, or any other characteristic protected by law. UnitedHealth Group is a drug-free workplace. Candidates are required to pass a drug test before beginning employment. Job Keywords: IT Project Manager, Healthcare Payer Consulting, healthcare, consultant, consulting, strategy, project, program, deliverables, client, account, growth, relationships, Eden Prairie, MN, Chicago, IL, Basking Ridge, NJ, insurance, consulting, IT projects, IT programs, Client facing, Aetna, Cigna, Humana, Express Scripts, Anthem, Blue Cross, Blues
Restaurant Team Member Open Interviews - Holmdel, NJ
Chipotle Mexican Grill - Holmdel, NJ
Mar 18, 2017
Restaurant Team Member Open Interviews - Holmdel, NJ (17007586)Descriptionhttp://flexbooker.com/chipotle/2566EVENT DATE: 03/29/17EVENT...
Restaurant Team Member Open Interviews - Holmdel, NJ (17007586)Descriptionhttp://flexbooker.com/chipotle/2566EVENT DATE: 03/29/17EVENT TIME: 9am – 11am, 3pm – 5pm Schedule your own interview. You’ve been invited to join us at an open interview event in Holmdel, NJ on Wednesday, Mar. 29th. We'll be hiring for multiple open positions. Interviews will be held from 9am – 11am and 3pm – 5pm at our restaurant located at 2131 Rte 35, Holmdel, NJ 07733. To register for an interview, click the ‘Register’ button and select a time slot that works for you.To prepare for your interview, you can learn more about careers at Chipotle here. Our Crew members take pride in preparing and serving Chipotle’s delicious food. By consistently following the proper recipes and procedures, and adhering to Chipotle’s high standards regarding food preparation, sanitation, teamwork and customer service, they help to ensure that the Chipotle customer experience is always the best it can be. Crew members’ responsibilities require them to be on their feet working while clocked in. At Chipotle we don't have multiple job titles for our entry level employees but all of our crew will play the role of dishwasher, cashier, server, host, bartender, cook, prep cook, etc. so be prepared to learn a lot and work hard if you join the team.Primary Location: New Jersey - Holmdel - 2566 - Holmdel-(02566)Work Location:2566 - Holmdel-(02566)2131 Rte 35Holmdel 07733
Become an Uber Driver Partner - Instead of Cashier
Uber - Woodbridge, NJ
Mar 24, 2017
Uber Driving Partners Who we are: Drive with Uber and get paid weekly in fares by helping our community of riders get around town....
Uber Driving Partners Who we are: Drive with Uber and get paid weekly in fares by helping our community of riders get around town. Driving with Uber is a great way to earn cash on your schedule. The more you drive, the more you can earn. It's simple and perfect for those looking for seasonal, work from home, entry level, temporary, or any type of job opportunities. What you need to know: Earn Great Money: The more you drive, the more you can earn. Flexible Schedule: Make your own schedule as a contractor – any time day or night. Getting Started is Easy: Signing up is quick & easy – no experience required! Get Paid Weekly: Get checks deposited into your bank account weekly. Requirements: You're at least 21 years old You have a 4-door vehicle You have a driver’s license and insurance You're friendly and excited to earn money on your schedule! Additional Information: If you have previous employment experience in transportation (such as a delivery driver, driver, professional driver, driving job, truck driver, heavy and tractor-trailer driver, cdl truck driver, class a or class b driver, local truck driver, company truck driver, taxi driver, taxi chauffeur, cab driver, cab chauffeur, taxi cab driver, transit bus driver, bus driver, coach bus driver, bus operator, shuttle driver, bus chauffeur) you might also consider partnering with Uber and earn great money. We also welcome drivers who have worked with other peer-to-peer ridesharing or driving networks like Lyft, Sidecar, Deliv, Postmates, Roadie. Our driver partners come from all backgrounds and industries ranging from traditional driving and transportation industries to other industries.
Sales Associate - $1000.00 Sign-on Bonus!
DISH Network - Roseland, NJ
Mar 15, 2017
How would you like to work for a FORTUNE 250 and Fortune Most Admired company with an abundance of resources available for training,...
How would you like to work for a FORTUNE 250 and Fortune Most Admired company with an abundance of resources available for training, support, marketing, compensation, and advancement? Would you like to take 100% inbound calls, with absolutely no cold-calling?! Pay is an hourly base rate PLUS uncapped commission! The average total compensation is 50k-60k and top performers are earning over $100,000! Why should you start a career as an Inside Sales Associate at DISH?Those new to sales love the experience of selling for a FORTUNE 250 company, with fully PAID TRAINING, and continual developmentSell for the #1 company in Customer Service, Satisfaction, Programming, Value and TechnologyFULL BENEFITS PACKAGE:Medical, Dental and Vision401K with company match + profit sharingPaid time off- vacation, sick, and HolidaysLife and short/long term disability insurance Discounted Employee Stock Purchase programTuition ReimbursementFREE DISH PROGRAMMING (YES, that includes HBO, Showtime, and Cinemax!)High-end Rewards and Recognition program and MORE!*$1000.00 sign-on bonus applicable at 90 days of employment. Details will be discussed throughout interview process.Having these qualities would make you a great fit:Assertive and results-oriented with a NEED TO SUCCEEDA desire to answer INBOUND sales inquiriesMoney motivated; aiming to maximize our UNLIMITED EARNING POTENTIALEnjoy helping customers choose the best package for their needsComfortable interacting with a diverse potential customer baseHigh school diploma or general education degree (GED) preferred; or 3 months of related experience and/or training; or equivalent combination of education and experienceCareer Path Opportunities: We love to promote employees from within and have several career path opportunities to choose from: Customer Retention- after 3 months of employment as an Inside Sales Associate, you’ll be eligible to apply to become a Customer Retention Specialist, one of the next roles on our career ladder. The main responsibility of a Customer Retention Specialist is to educate current customers on why they should stay with DISH. We consider customer retention calls to be the most important call type that our specialists take and we’re looking for experienced sales associates to promote in to this role. Customer Retention Specialists have the ability to earn even more money with our uncapped incentive plan. Inside Sales SupervisorA variety of other roles at DISH within departments such as Training, Operations, Customer Service and CorporateYou will be responsible for new customer growth by sharing your knowledge and enthusiasm about our pricing, service, and technology. Our Sales Representatives typically talk with 25 – 30 potential customers per day, nationwide. By building quick rapport and using your assertiveness and confidence, you’ll educate prospective customers on why they should choose DISH! You should feel comfortable overcoming objections, have a desire to constantly learn, and be willing to accept feedback. We need driven individuals who can adapt as we continue to grow and who are motivated to advance to handle new responsibilities. Check out the video below to learn more about our team!http://careers.dish.com/career-choices/sales/ For more information, please click here. #LI-KC1 Roseland, NJ
Cumberland Therapy/MyTherapyCompany/AlphaVista - Newark, NJ
Mar 21, 2017
Cumberland Therapy is interviewing now for the 17/18 SY Speech-Language Pathologists for our school-based openings in Newark, NJ. We...
Cumberland Therapy is interviewing now for the 17/18 SY Speech-Language Pathologists for our school-based openings in Newark, NJ. We offer local clinical support, comprehensive benefit packages and fantastic teams in the area! Serving grades K-12 8am-3pm schedule NJ SLP License, NJ DOE, and NJ CHR required We are part of The Stepping Stones Group, which includes special education brands such as; MyTherapyCompany, AlphaVista, Cumberland Therapy and Pathways to Speech. We work in some of the largest districts throughout the US, with access to our clinical teams for onsite support and guidance. We can offer you: Mentoring & Support through our Foundations for Success Program Relocation and Housing Assistance Travel Packages for our SLPs and CFs CEU allowance and FREE Webinars! Join our amazing team today!
RN-PACU - Travel Nursing: PACU Travel Nursing Opportunity in Jersey City, NJ.
RNnetwork - Jersey City, NJ
Mar 22, 2017
Come work for RN NetworkWe are seeking an experienced and self-motivated PACU Registered Nurse to join our growing team of nursing...
Come work for RN NetworkWe are seeking an experienced and self-motivated PACU Registered Nurse to join our growing team of nursing professionals! PACU RN’s will assist in recovering the patients from anesthesia. They will also monitor patients while they wake up from surgery until they are released, either by discharge to outpatient or transfer to the floor for their patient stay. PACU RN’s provide effective communication to patient/family, team members, and other healthcare professionals for all PACU patients. Call our friendly recruiters today!Customized benefits package with the pay and insurance coverage you need, beginning day onePaid private housing and utilities, and reimbursement for travelReimbursement for licensing and certificationWhy choose RNnetwork?
Hired - New York, NY
Mar 21, 2017
Are you a Ruby Developer? Are you experienced with managing the interchange of data between the server and the users?Your primary focus...
Senior Scientist, Translational and Diagnostic Informatics
Celgene - Summit, NJ
Mar 22, 2017
DescriptionTranslational Development at CelgeneCelgene Corporation, headquartered in Summit, New Jersey, is an integrated global...
DescriptionTranslational Development at CelgeneCelgene Corporation, headquartered in Summit, New Jersey, is an integrated global biopharmaceutical company engaged in the discovery, development and commercialization of novel therapies for the treatment of cancer and inflammatory diseases. At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients. Investigational compounds are being studied for patients with hematological and solid tumor cancers, including multiple myeloma, myelodysplastic syndromes (MDS), acute myeloid leukemia (AML), chronic lymphocyte leukemia (CLL), non-Hodgkin's lymphoma (NHL), pancreatic cancer and lung cancer. Translational Development is a department within the Research and Development organization that facilitates the transition of drug candidates from drug discovery through early- and late-stage clinical development. Early-stage translational development activities enable rational determination of dose-schedule and responsive patient populations, based on deep understanding of drug mechanism of action. Late-stage translational development activities build upon the early work, additionally exploring mechanisms of resistance, rational drug combinations and product differentiation. The late-stage translational development function is responsible for the development of translational strategies to support the development, and maximize the potential, of Celgene therapies post-clinical proof-of-concept, including registrations and life-cycle management.Summary/ScopeDual reporting to Translational Development and Research Analytics, the candidate will be part of the late stage translational development group based in either Northern New Jersey or San Francisco bay area California. We seek a talented, collaborative computational scientist to lead work on the analysis of high-dimensional tissue, cell and molecular profiling data. The successful applicant is expected to play a key scientific and strategic role leveraging innovative computational analysis strategies and rich patient data to empower data-driven decisions for development programs in Celgene's clinical portfolio. Scientific activities associated with this position range from provision of deep insight into therapeutic mechanisms of action for existing therapies and novel therapies in clinical development, identification and predictive leverage of patient phenotypes associated with therapeutic effect and outcome in key indications, and development of molecular biomarker hypotheses for implementation into clinical trials as potential diagnostic tests. Data will originate from a wide range of cellular and molecular profiling platforms, including transcriptomic, proteomic, genomic, functional and immunophenotypic assays.The role offers the opportunity to directly impact the delivery of transformational therapies in key diseases of unmet medical need, particularly in lymphoid and myeloid diseases. Strong interest in the inter-disciplinary application of computational analysis methods to life sciences data is imperative. ResponsibilitiesWorking in collaboration with computational, biological and clinical scientists across the Celgene Research and Development organization, responsibilities include but are not limited to:•Active participation as a core team member in the Translational Development and Diagnostics Department and RIKU Research Analytics group. •Participate in cross-functional disease teams in the identification of clinically-relevant patient segments by analysis of public and proprietary biomarker and clinical data. •Guide development of molecular patient selection and biomarker hypotheses towards clinical diagnostics. Work closely with Translational Diagnostics scientists to develop molecular assay strategies. •Prioritize across projects and take responsibility for delivery of research output to agreed objectives and timelines. Author scientific reports, with methods, results and conclusions presented in a publishable standard.•Apply novel computational analysis and biological interpretation approaches to leverage internal, public and partner datasets and empower data-driven decisions across therapeutic programs.•Multi-disciplinary collaboration to investigate compound and disease properties, influence decision making across the translational research and clinical development process, and feedback to inform early development of novel therapies.•Data integration across assay platforms and knowledge transfer from pre-clinical experiments to clinical trials. •Contribution to planning and execution of collaborative projects with leading academic and commercial research groups worldwide.#LI-JB1QualificationsBackground experience & complementary knowledge •A Ph.D. in computational biology, bioinformatics, or related field from a recognized higher-education establishment. 2+ years experience in pharma/biotech research environment preferable. •Track record of peer-reviewed publications in top-tier scientific journals•Experience in quality assessment, analysis, interpretation and visualization of terabyte-scale datasets, including high-throughput sequencing data•Expertise in algorithmic implementation, statistical programming and data manipulation, using e.g. R/Bioconductor and contemporary, open-source bioinformatics tools and database structures. Preference given to candidates with a track record of developing portable algorithms that can be shared with peers•Proven expertise in the development and / or implementation of algorithms to distill, analyze and interpret complex datasets, particularly those associated with pharmacogenomics and biomarker discovery•Proven problem-solving skills, collaborative nature and adaptability across disciplines.•Excellent verbal and written communication skills. Fluent verbal and written English language skills prerequisite.Celgene iscommitted to equal opportunity in the terms and conditions of employment forall employees and job applicants without regard to race, color, religion, sex,sexual orientation, age, gender identity or gender expression, national origin,disability or veteran status.Celgene complies with all applicable national,state and local laws governing nondiscrimination in employment as well asemployment eligibility verification requirements of the Immigration andNationality Act. All applicants must have authorization to work for Celgene inthe U.S
Front Desk Agent
Concierge - New York, NY
Mar 24, 2017
Description The Front Desk assumes a pivotal role in every logistical operation relating directly and indirectly to overall guest...
Description The Front Desk assumes a pivotal role in every logistical operation relating directly and indirectly to overall guest satisfaction and the ultimate success of the hotel. Responsible for greeting guests, check-in and check-out, reservations and concierge services. Requirements: Kind and intelligent demeanor. Knowledge of Opera is a plus Comprehensive knowledge of New York Required experience: Hotel Experience: 1 year or related field.
Sr. Associate, Clinical Research
Impax Labs - Middlesex, NJ
Mar 14, 2017
Summary of Duties and Responsibilities Support the Generic Product Development Department and Biopharmaceutics Group in the initiation,...
Summary of Duties and Responsibilities Support the Generic Product Development Department and Biopharmaceutics Group in the initiation, maintenance and closure of Clinical Trials according to Good Clinical Practices (GCP), Good Laboratory Practices (GLP), the Code of Federal Regulations (CFR), and applicable Regulatory Guidance’s by performing the following duties. Key Accountabilities Serve as a central contact for communications/correspondence between the Generic Product Development, Biopharmaceutics Group, and CROs and other vendors. Review the study protocols and if needed help to design data collection from known case report forms (CFRs). Identify and assess the suitability of clinical and bioanalytical facilities for bioequivalence studies. Conducting general GCP and GLP audits. Maintain study schedules, request proposals/contracts from CROs, compare competiveness and work quality of the CROs, maintain study budgets, initiates CDAs with different vendors, process vendor contracts and ensures payments are sent on time to vendors. Monitor trials throughout their duration, which involves visiting the trial sites on a regular basis. Verify that data entered onto the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV). Write visit and audit reports. Analyze and interpret scientific data using Phoenix WinNonlin and other databases. Generate and track drug shipments and ensure timely delivery of final clinical and bioanalytical reports for regulatory submissions. Ensure all unused trial supplies are accounted for and stored properly. Perform duties such as bulk copying and faxing, and filing of correspondence, lab reports, Clinical Monitoring Reports, and other study documents. Assist coordination of study logistics, documents, drug shipments, enrollment and safety 5% Collect regulatory documents required for study initiation. Maintain central study files in a state of audit-readiness. Maintain reference products inventory list and order products when needed. Maintain reference products inventory list and order products when needed. Communicate regularly with Generic Products Development teams: provide information, track study randomization codes, reports, may follow up on problems identified during the study. Perform all responsibilities in accordance with Standard Operating Procedures, established guidelines and work instructions, appropriate industry and Good Clinical Practices, Good Laboratory Practice and Applicable Regulatory Guidance standards. Perform other duties as assigned by management. Work Requirements Education BS/BA degree required, health related field preferred.Experience 8 years of experience with medical terminology, GCP, GLP and Pharmaceutical Industry Regulatory guidelines is required. Special Skills 5+ years of demonstrated proficient with MS Office (Word, Excel, Access, and PowerPoint), email, internet, required. 2+ year of experience using computerized systems i.e., Phoenix WinNonlin, SAS, and other databases required. 2+ years of experience analyzing and interpreting scientific data and skilled use of computerized systems and databases required. Experience 8 years work experience in clinical and bioanalytical science environment required. Core Competencies Requires excellent organizational skills and ability to prioritize a variety of tasks. Requires careful attention to detail to be successful. Advanced understanding of data management processes required. Ability to communicate and work effectively with a diverse team of professionals required. Flexible and able to thrive in a fast-paced environment required. Express information to individuals or groups taking into account the audience and the nature of the information (e.g., explain technical concepts to non-technical audiences) required. Receive, attend to, interpret, understand, and respond to verbal messages and other cues required.
Licensed Real Estate Salesperson - copy
Metropolitan Property Group, Inc. - New York, NY
Mar 22, 2017
Description Take advantage of this exciting opportunity to work with one of Manhattan's top real estate firms! We are currently looking...
Description Take advantage of this exciting opportunity to work with one of Manhattan's top real estate firms! We are currently looking for both NEW and EXPERIENCED agents! We are looking for full-time, highly motivated, energetic individuals with an entrepreneurial spirit. This career is the perfect combination of flexibility and unlimited earning potential! Applicant must be licensed or enrolled in real estate school. You can absolutely begin training while still in school, so you can start getting hands on experience while you finish up your coursework and then hit the ground running! WHY JOIN METROPOLITAN PROPERTY GROUP? Established Firm : MPG has an established brand and is known throughout the industry as well as by consumers as an honest, sophisticated & professional firm. Training : Intensive introductory training that will cover all aspects of a real estate transaction including but not limited to Advertising / Lead Generation, Production Knowledge / Inventory, Qualifying / Closing Clients, Time Management / Relationship Building. We also provide ongoing guidance to help develop and strengthen unique individual business plans and teach our agents how to convert renters into buyers. Benefits No desk fees and competitive commission splits that increase over time Split advertising expenses (listing sites, banners, etc) paid up-front by company Training & development with experienced residential agents Numerous contacts with landlords and clients throughout the city 100% access to the Manhattan open listings market Daily client leads Unlimited advertising on our highly-trafficked website that syndicates directly to Naked Apartments, and 35 other marketplaces! Networking and prospecting using MPG proven systems and models Developing relationships that will work for you year after year Learning how to obtain and maintain exclusive listings of your own If you are interested in learning more about us and this exciting opportunity, please contact our management team, Angie or Ofira at 212-850-0940.
Research Associate-QC Biochemistry
Eli Lilly and Company - Branchburg, NJ
Mar 22, 2017
*Company Overview At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare...
*Company Overview At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. *Responsibilities Perform routine QC responsibilities as assigned by supervisor such as: •Lab Method stewardship and assay development for Capillary Electrophoresis–Sodium Dodecyl Sulfate (CE-SDS), capillary isoelectric focusing (CIEF), imaged capillary CIEF (iCIEF) •Conducting routine and non-routine analyses of test articles as assigned by supervisor by appropriate biochemical methods such as: SDS-PAGE, HPLC, CE-SDS, ELISA, Cell Based Bioassay, etc. •Demonstrate initiative to perform routine QC responsibilities such as sample coordination, lab equipment maintenance, QC document management, QC inventory control and reconciliation of sample requests/documents as needed. •Monitor laboratory equipment for temperature and conformance to specifications. •Apply acceptable cGMP practices during execution of all work tasks. •Work independently with moderate supervisory guidance. Exhibit strong teamwork skills. •Update supervisor of progress on frequent basis. Seek additional guidance as needed. Perform independent assignments such as: •Compile data for documentation of test procedures and preparation of reports. •Conduct document reviews and author standard operating procedures (SOPs). *Travel Percentage 0-10%*Basic Qualifications •Bachelor's Degree in a related science such as a Biology or Biochemistry with minimum 7 yrs experience, or Master's Degree in a related science such as a Biology or Biochemistry with minimum 5 years’ experience •Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position. Additional Skills/Preferences •Good working knowledge of cGMP regulations is required. •Ability to work independently with moderate supervisory guidance. •Excellent teamwork and communication skills. •Attentive to detail. •Good computer skills. Additional Information Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Executive Director, Clinical Research Physician CART
Novartis Oncology - East Hanover, NJ
Mar 19, 2017
Novartis Oncology is a leader in discovering, developing and marketing innovative drugs for patients with cancer and, due to rapid...
Novartis Oncology is a leader in discovering, developing and marketing innovative drugs for patients with cancer and, due to rapid growth, we are seeking a board certified oncologist/hematologist with BMT experience and Clinical Research experience and interest to join our successful and growing US CDMA organizationThe ideal candidate will provide strategic medical and scientific leadership in the CTL019 program, including new therapeutic areas. This position encompasses national studies and research projects. The candidate will also be involved in any US launch activities related to CTL019.The successful candidate will direct US clinical activities including:• Serve as U.S. Executive Medical Director for global clinical development trials and/or U.S. Medical Affairs Trials (including both Novartis Sponsored and Investigator Initiated) in the therapeutic area of CART.• Manage a team of 2-4 MDs and 4 clinical scientists• Design and optimize clinical trial design and ensure clinical trials meet ethical and regulatory standards;o Develop US specific clinical research plan for CTL019 in the areas of malignant hematology (eg. Pediatric ALL and DLBCL) that compliments global plan;o Medical support regarding the execution of launches in the US for CTL019;o Conduct medical review and interpretation of efficacy and safety data from clinical trials.• Responsible for the quality, coordination, medical accuracy, and timeliness of clinical study reports, responses to clinical questions from Health Authorities or IRBs related to sponsored studies within EDSI, and other documents for external or internal audiences related to EDSI sponsored studies.• US representative on CART GPT;• US Medical expert for review and feedback to Global Protocols and Global Development Plans.• Develop strategy for US CTL019 studies including exploratory indications and integrate US plan with overall Global strategy. Oversee the review and approval of IIT concepts. Oversight during the conduct of trials including safety monitoring. Review of interim and final publication, manuscripts, or abstracts.• Supervise and manage individuals on the EDSI team as appropriate. Lead the Clinical Team, including interactions with Safety, HEOR, Marketing, Regulatory, Research, and other functions.• Review and approve abstracts publications & manuscripts for Investigator Initiated Trials to ensure clinical accuracy and appropriate safety review.• Present and discuss data and findings at relevant internal and external meetings.• Ensure adherence to GCP/ICH and company Standard Operating Procedures (SOPs).• Assist in the development and appropriate spending of US CART clinical budget.• Extensive interactions with academic thought leaders to optimize clinical trial strategies.• Extensive interactions with other functional teams including HEOR, Medical Information, Scientific Communication, Commercial, Regulatory and others, to refine compound strategy and projects.• Coach and train internal colleagues as requested.• Medical liaison on CTL019 with US commercialEEO Statement The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.• MD, or equivalent required. Board Certified in either Hematology required, with clinical experience in stem cell transplantation preferred.• At least 7 years of experience in Hematology clinical research in the pharmaceutical industry OR experience in clinical research or medical affairs is preferable or a combination of experience in academic medicine with clinical research and or clinical development experience in collaboration with the pharmaceutical industry.• Scientific medical research experience in Oncology, Hematology and or transplantation (or relevant specialty) with demonstrated record of scientific medical publications.• Experience leading the design, conduct, analysis and reporting of clinical studies is strongly preferred.• Superior leadership, networking, collaboration and communication skills.• Successful interactions with Medical Experts and investigators.• Demonstrated the capability for strategic planning along with operations skill and experience related to clinical research involving both single and multiple centers.• Ability to work across multiple functions is essential.• Effective oral and written communications skills and strong leadership are essential for success in the role.
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