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  1. Senior Medical Writer

    Must have: Strong Phase III regulatory writing experience AND PK/PD Phase I writing experience Therapeutic area experience in: oncology and/or endocrinology Duties and Responsibilities   % of Time Provide medical writing support for development programs by hands-on writing of protocols, IBs, and CSRs. Participate in appropriate development teams and internal strategy and operations meetings. 60% Manage/Assist documents through the review process (coordinating ...

  2. Data Analyst - Pricing and Reimbursement Group

    Our client, one of the major pharmaceutical companies located in Princeton, NJ, is seeking a Data Analyst for a 6 month contract assignment. Primary Job Description and Responsibilities: The Pricing & Reimbursement group provides Medicaid, Chargeback, Rebate Processing, and Government Reporting services for the US Pharmaceutical business. The team is working on various projects including a major system upgrade while at the same time maintaining daily activities at the current service level. This ...

  3. PhD Staff Chemist - Conductive Materials, Photovoltaics, Displays

      PhD in either Glass Science, Ceramic Engineering, Inorganic Chemisty or Materials Science 1-2 years experience. The R & D team located in Union, NJ performs research on conductive materials and technologies used in photovoltaics, displays and other electronics applications.   Responsibilities include but are not limited to: -Perform Research and Development activities in the field of glass science.  Candidate will interact with an international technical team.  -Formulate, melt and characterize ...

  4. Compound Pharmaceutical Sales Representative

      If you have experience selling compound pharmaceuticals and desire a generous & predictable income from stable pharmacies then please read on. We have clients that are looking for ethical, career minded reps that have established relationships with physicians who believe in and are currently prescribing compounded pharmaceuticals to their patients. We would prefer reps that have current relationships but will consider former compounding reps with less than a 12 month time gap out of the business. ...

  5. Compound Pharmaceutical Sales Representative

      If you have experience selling compound pharmaceuticals and desire a generous & predictable income from stable pharmacies then please read on. We have clients that are looking for ethical, career minded reps that have established relationships with physicians who believe in and are currently prescribing compounded pharmaceuticals to their patients. We would prefer reps that have current relationships but will consider former compounding reps with less than a 12 month time gap out of the business. ...

  6. Compound Pharmaceutical Sales Representative

      If you have experience selling compound pharmaceuticals and desire a generous & predictable income from stable pharmacies then please read on. We have clients that are looking for ethical, career minded reps that have established relationships with physicians who believe in and are currently prescribing compounded pharmaceuticals to their patients. We would prefer reps that have current relationships but will consider former compounding reps with less than a 12 month time gap out of the business. ...

  7. Genetics and Dairy Reproductives Sr. Marketing Manager

    The Sr. Marketing Manager will lead all Marketing efforts related to our client’s genetics and reproductive brands. The incumbent will lead the development of a rolling operational plan, including marketing objectives and strategies, segmentation brand positioning, pricing, brand life cycle planning, distribution, promotion and competitive action for assigned brand. Qualifications include BS or BA required. MBA or relevant advanced degree preferred. Professional experience: Five to seven years of ...

  8. DESKTOP PUBLISHER

    Our client, a large pharmaceutical company, is currently seeking a DESKTOP PUBLISHER.Responsible for publishing and managing QC for high quality scientific documentation (e.g. study reports) for submission to regulatory authorities in support of marketing applicationsPreparation of high quality scientific documentation and submission documents in accordance with the timelines specified by NIBR and in compliance to internal and external standards Completion of an adequate number of nonclinical or ...

  9. Analytical Biochemistry CRO Administration Manager - Princeton, NJ

    Seeking Ph.D. in biochemistry, toxicology, bioanalytics or similar field and 10 + years of experience managing pharmaceutical development bioanalytics projects using Contract Research Organizations. Must have thorough knowledge of scientific operations, management, technical and administrative functions of the laboratory. Shall: *** Sources, qualifies, hires and directs CRO core activities, including method development, method validation and sample analysis for global regulatory submission. *** ...

  10. HR Employee Services Coordinator-Regular JFT

     HR Employee Services Coordinator The HR Employee Services Coordinator will be responsible for providing excellent customer service support in the area of Human Resource transactions, policies and processes to all employees through multi-channel support (i.e., phone, online, email, etc.) etc. This role is within the Human Resources Employee Services Center and provides support to employees, HR Business Partners, and other Centers of Excellence (CoE) within HR. This role provides a "live voice” to ...

  11. Clinical Research Scientist

     **BA/BS or advanced degree required! 3 years of experience required!** Duties:  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 ...

  12. Desktop Publisher

    Hello,   My name is Bryson Jackson and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Desktop Publisher (s) for a prominent client of ours.  This position is located in East Hanover, NJ. Details for the positions are as follows:   Job Description: LONG TERM CONTRACT!!!! FORTUNE 500 CLIENT!!!! Duties               Responsible for publishing and managing QC for high quality scientific documentation (e.g. study reports) for submission to regulatory ...

  13. Consumer Scientist 162.14KO

    :: If you meet the qualifications listed below and would like more information contact Kristine at 815-756-1221. Attach resume when responding to this posting :: The scientist will be responsible for contributing towards the development of consumer preferred products from concept ideation through to realization. Qualifications: -BS/BA (5 years of experience, MS (3 years of experience), or PhD (1 year of experience) in science/consumer science/sensory science -Experience in consumer research -Strong ...

  14. Quality Manager 164.14KO

    :: If you meet the qualifications listed below and would like more information contact Kristine at 815-756-1221. Attach resume when responding to this posting :: The manager will be responsible for the fulfillment of corporate directives and management requirements to ensure sustainability of site compliance. Qualifications: -MS/PhD -Agribusiness, chemistry, biology, engineering, or feed/food technology qualifications required -Intimate knowledge if quality systems, preferably within DNP or feed ...

  15. 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 ...

  16. 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 ...

  17. 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, ...

  18. 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., ...

  19. Mgr - QAIG Lab Support

    Actavis, Inc. Job Purpose The QA Manager of Laboratory Systems Support is responsible for the general oversight of Actavis Laboratory Systems specific (but not limited) to Deviations & CAPAs (non-lab), Complaints, Laboratory Equipment/Utilities Qualifications, Change Control, Method Validation, and Analytical Documentation. Description of KEY responsibilities: * Manage the QA Laboratory Systems Support department while maintaining a high quality standard in accordance with GMP, SOP, FDA and OSHA ...

  20. Head of Global Quality Management

      As Head of Global Quality Management in the Quality Assurance group, you will report to the Regulatory Affairs Director and coordinate the implementation of the Global Quality Management and Assurance strategy for the Scientific Division and Phase IV studies. You will supervise more than 20 employees worldwide (Europe, North America, and Asia).  Accountability Responsibilities: Implement the quality systems to fulfil regulatory requirements applicable to Company (GLP, GCP, GMP, GDP) Define ...

  21. 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 ...

  22. 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), ...

  23. 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 ...

  24. Senior Medical Writer (home based)

      Regulatory Medical Writer Must have written all of the following: NDA submissions, Protocols, Narratives, Case Report Studies, and Inform Consent forms   Write clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical ...