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  1. Clinical Research Scientist - 105034

    Clinical Research Scientist – 6 month contract, East Hanover, NJ The team is looking for highly motivated and pleasant individuals with previous experience a clinical trial site in a global pharma company or those with experience in conducting a global study. We have a strong preference for those with a strong scientific or clinical background (i.e., oncology nurse, pharmacists, etc) and those with prior data management experience. This experience will be of help in the entry and review of patient ...

  2. Desktop Pubishler - 105033

    Desktop Publisher – 6 month contract Responsible for publishing and managing QC for high quality scientific documentation (e.g. study reports) for submission to regulatory authorities in support of marketing applications. Preparation of high quality scientific documentation and submission documents in accordance with the timelines specified by Novartis Institutes for BioMedical Research (NIBR) and in compliance to internal and external standards. Key Performance Indicators (KPIs):  Completion ...

  3. Biostatistician III - 105029

    Biostatistician III – 6 month contract Designing clinical studies. Writing and reviewing statistical sections and other relevant parts of study synopses and protocols. Support study start up activities. Develop RAP, program TLFs, preparation for database lock, dry run and CSR activities. Review CRF, DB spec, VAP. Support analyses as required for decision making at project level. Support analyses and activities during submission and response to HA questions. Coordinate study tasks with other ...

  4. Clinical Research Manager II -  105023

    Clinical Research Manager II – 6 month contract Support US efforts in the planning, execution and reporting of US Clinical Data and Medical Affairs (CDMA) clinical trials in Oncology: Implementation of clinical trials in the United States (safety, data consistency, trial timelines, budget, resources, eligibility and enrollment), within a cross functional team and with oversight from the Associate Director.  Interfacing with the hematology therapeutic area global and US clinical team members, ...

  5. Clinical Research Scientist

    The Fountain Group has an IMMEDIATE opening for a Clinical Research Scientist in east Hanover, NJ. Qualified candidates should submit an updated resume along with contact information to be considered.   Overview The team is looking for highly motivated and pleasant individual with previous experience at a clinical trial site in a global pharma company or those with experience in conducting a global study. We have a strong preference for those with a strong scientific or clinical background (i.e., ...

  6. Biostatistician

      Hello,   My name is Donald and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Biostatistician III for a prominent client of ours. This position is located in East Hanover, NJ. Details for the positions are as follows:   Job Description: Designing clinical studies. Writing and reviewing statistical sections and other relevant parts of study synopses and protocols. Support study start up activities. Develop RAP, program TLFs, preparation for ...

  7. Process Engineer

    POSITION TITLE: Process Engineer   SPECIFICATION NUMBER:  68804CRI   LOCATION: Morristown, New Jersey   COMPENSATION:    Hourly Consultant - 9 months contract  - then possibility to cross over to a permanent position paying up to $90,000 +  16% Bonus   COMPANY:    Our client is a leader in the Medical Device industry.   POSITION SUMMARY   This is an opportunity to play a key-role in an aggressive, growth-oriented Company that provides an entrepreneurial work environment in an emerging ...

  8. Managed Care Contract Analyst III

    We have a Contract opportunity with a prominent client for a Managed Care Contract Analyst III in East Hanover, NJ.   Duties:              Accurately enter contracts and maintain membership for various market segments into Model N and SAP, to ensure accurate data availability to allow for flexible and meaningful management reporting, chargeback processing and rebate adjudication. Conduct peer review sessions. Possess knowledge in managed care, specialty pharmacy, and Medicare market segments ...

  9. Researcher

    QPharma is growing.   We currently have an opening for a Researcher, to work in our corporate headquarters located in Morristown, NJ. Duties and Responsibilities: The Researcher’s duties will involve researching all 50 state laws and rules and regulations around prescriptive authority for controlled substances. The Researcher would need to be well informed of the current regulations as they exist within the 50 states, and continually track any updates/changes to the laws.  The information to be ...

  10. Registered Pharmacist ( Per Diem)

    Registered Pharmacists ( Per Diem) QPharma is expanding its pharmacy operations and services.  We are looking for  NJ licensed and Registered Pharmacists to work per diem in support of our closed door specialty/mail order facility.  Our facility  has a high volume prescription intake, and the Pharmacists will also provide trouble shooting of insurance related issues, and QA of prescriptions to get dispensed. Required Must be a Registered Pharmacist and licensed in the state of NJ Be able to ...

  11. Senior Account Executives

    QPharma, Inc., is growing!  We have openings for Senior Account Executives within our Commercial Services division.  In this role, the Senior Account Executive will report to the Client Services Manager and provide leadership to other team members. The Senior Account Executive will be a strategic, smart communicator who develops, builds and maintains strong relationships with clients. Duties and Responsibilities: Responsible for overall client satisfaction as it relates to the services provided. ...

  12. Clinical Manager III, Oncology - 105024

    Expert Clinical Manager III – 5 month contract Responsible for all operational aspects of 1 or more Office of Generic Drugs (OGD) clinical trial(s) under the leadership of Clinical Trial Head (CTH).  Support all scientific aspects of clinical trial(s) as assigned.  Responsible for program level activities as assigned. Ensure all operational trial deliverables are met according to timelines, budget, operational procedures and quality standards. Provide input and contribute to the development of ...

  13. Nonwovens Scientist – NONWOVEN, Consumer Research - Ramsey, NJ

    STI-ECD-561-(A) Nonwovens Scientist – NONWOVEN, Consumer Research - Ramsey, NJ Location: Ramsey, NJ Domain: Textile Job Type: Direct                           Job Description: Nonwovens Scientist will assist the Manager in the development and implementation of unique and advantaged technologies to support the product roadmap.   Job Responsibilities: The Staff Scientist will be exposed to technical intellectual property on a frequent basis. Expected to initiate/establish Confidentiality ...

  14. Clinical Research Manager II- 94440

    Minimum Requirements: Prior experience with Implementation of clinical trials in the United States safety, data consistency, trial timelines, budget, resources, eligibility and enrollment.   Education: Bachelor Degree required   Job Description: Support US efforts in the planning, execution and reporting of USCDMA clinical trials in Oncology. Implementation of clinical trials in the United States (safety, data consistency, trial timelines, budget, resources, eligibility and enrollment), ...

  15. SENIOR DEVELOPMENT ENGINEER: ROOFING SYSTEMS

    You are a pro at materials selection and product development for membrane roofing and waterproofing systems; that’s why we need you to help keep us at the top of outgame! You will work with the R&D team as well as cross-functional groups to develop new products from inception through commercialization. Help us to identify new product, process and raw materials developmental opportunities for waterproofing, components and accessories. Use design of materials to plan and perform testing and ...

  16. Clinical Research Manager II

    We have a Contract opportunity with a prominent client for a Clinical Research Manager II in East Hanover, NJ.   Duties               Support US efforts in the planning, execution and reporting of USCDMA clinical trials in Oncology. Implementation of clinical trials in the United States (safety, data consistency, trial timelines, budget, resources, eligibility and enrollment), within a cross functional team and with oversight from the Associate Director. Interfacing with the hematology ...

  17. Sr Manager Field Sales Operations - Pharmaceutical

    NEW Position- Sr Manager Field Operations Experience: 3 - 5 years of pharmaceutical sales operations Compensation: $120,000.00 - $145,000.00 Job Description: The Senior Manager of Field Operations is responsible for the development, analysis, and implementation of sales force strategy and tactics to include resource optimization, field force size and structure, targeting, alignments, personnel placement and call planning. JOB DUTIES AND RESPONSIBILITIES Serve as key liaison between field ...

  18. Pharmacovigilance Submission Specialist -Contract

    Our institution is currently seeking a US Pharmacovigilance Submission Specialist Consultant. The Submissions Specialist, US Pharmacovigilance (PV) role is accountable for the final step in the single case handling process for Pharmaceuticals products. The Submissions Specialist determines whether or not any marketed or clinical development case should be submitted to the FDA. This process involves analyzing case information for report ability based on US labeling, causality, drug code and regulatory ...

  19. Regional Clinical Research Associate III - 104998

    6 MONTH CONTRACT CANDIDATES WILL WORK FROM HOME AND CAN LIVE IN NJ, NY, MA This position is unique as it will be part of our Oncology Flexible Workforce and assignments will be made based on current needs and proactive planning that includes both short-term and long-term projects.  The candidate must be willing to travel regionally and to other areas for various assignments in the Eastern or Central U.S. as they arise. Depending on the project, there may also be some travel throughout the U.S., as ...

  20. Product Manager

    Position: Product Manager Company:  Manufacturer of Scientific Products for use in laboratory environments End Users: Laboratories in College/University, Biotech, Research, Pharmaceutical and Government accounts Requirements: BS degree in Marketing or one of the Sciences (Chemistry, Biology, etc.) 2-5 years past experience in a Marketing role - prefer Product Manager Base salary: up to $75,000 based on experience Full Benefits package  

  21. SAS Programmer

    Candidates MUST be able to complete a 6mo-1 year assignment. Extension past this time is possible but not guaranteed. No OT, No Travel required. All work to be performed onsite in Madison, NJ DESCRIPTION: Performs all SAS programming required for clinical trial analysis and reporting; Ensures that activities and processes performed are conducted according to sponsor requirements; Works closely with the Biostatistics and Data Management departments on various clinical projects; Leads programming ...

  22. SAS Programming Contractor

    This position will work with statisticians and other programmers for the ad hoc analysis for the product Nexium by following PCH programming process and Pfizer SOPs as well as the regulatory guidelines. The candidate should have strong SAS programming skills in clinical trials in the environment of the pharmaceutical industry. The candidate should have MS in math, or statistics or computer science.   Additional project based assignment linked to PWR9489, please do not submit candidates from PWR9489 ...

  23. Program Manager

    Strong planning, tracking, and follow-up skills - Proficient in Excell (including ability to understand programming) Job Description: Summary: The Clinical Program Manager will work cross functionally to develop, track and maintain timelines, resource needs and Key Performance Indicators/Key Quality Indicators across clinical development, coordinate clinical program reviews and support the team in ensuring adherence to clinical program plan. Job Responsibilities: • Enter and maintain resources ...

  24. Medical Writer

    OB SUMMARY The Medical Writer will apply analytical skills, functional literacy and expertise in document preparation including Clinical Study Reports, clinical overviews, integrated analyses of safety and efficacy, regulatory briefing books, key sections of the Investigator s Brochure. May also, in collaboration with the Project Team, assess document requirements, complexity, and potential issues with a submission, and develop strategies to deal with these, and lead a team of internal and external ...