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Biotech, R&D, & science in Fairfield

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    1. Sr. Technologist - Snacks 359.15TS

      :: If you meet the qualifications listed below and would like more information contact Tamra at 815-756-1221. Attach resume when responding to this posting :: The Sr. Technologist will be responsible for the coordination and execution of product development efforts for snack initiatives. Qualifications: -BS food science, food process engineering, or chemical engineering with product ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    2. In-House Clinical Trial Master File/Investigator Site File Specialist

      Minimum Requirements:  May have worked at a site and directly managed documents in the ISFCan also have sponsor experience building the ISF3-4 years experience working with ISFsBachelor’s degreeAble to work on-site.Proven strength in collecting/generating metrics for document systemsIncludes expertise in Excel charting, Visual Basic and SQL programminginVentiv Health Clinical LLC, an inVentiv ...

    3. Quality Control Technician

      Kelly Services has provided outstanding employment opportunities to the most talented individuals in the marketplace. Today, we are proud to offer an immediate short term contract opportunity for a Quality Control Laboratory Technician. This position is for a period of 5-10 weeks and is with a top Medical Device manufacturer located in North Haven, CT.SUMMARY OF POSITION: Support the Post ...

    4. Associate Director of PK and Clinical

      The Associate Director, PK & Clinical Research is responsible for leading the set-up, implementation, conduct, analysis and reporting of clinical trials for US and Global (Canada, EMEA & Innovative) projects. Defines the clinical trial strategy and management of BA/BE clinical studies. Responsible for the designing, planning and outsourcing of phase I-IV studies in support of Global ...

    5. Research Associate III- Cell Culture Ardsley NY

      The Research Associate III temp will be responsible for the preparation and maintenance of cell cultures, and production of protein expressed by cell cultures.This position will be responsible for serving as an active member of a multidisciplinary Research & Development team.Essential Duties and Responsibilities include the following. Other duties may be assigned. • Following supervision of R ...

    6. Medical Lab Technologist

      An Associate's degree in Medical Technology is required, Bachelor's degree is preferred or equivalent. MT or MLT (ASCP or equivalent) certification required. Minimum of one year of laboratory experience performing clinical chemistry, hematology, immunoassay, coagulation, and urine analyses. Two to three years of Phlebotomy experience preferredPerform all routine and special clinical chemistry ...

    7. Sr. Manager Clinical Research

      Manager/Sr. Manager, Clinical Research                              Be sure to check out all of our other current openings at www.scientificsearch.comSummary:The Manager/Senior Manager, Clinical Research ensures that clinical studies are conducted and data is generated, documented and reported in compliance with the study protocol, Good Clinical Practice (GCP), Good Laboratory Practice (GLP), ...

    8. Lead clinical research asocciate

      ~~DUTIES – RESPONSIBILITIES:The Lead Clinical Research Associate (LCRA) is responsible for the performance of assigned Field Based Clinical Research Associates (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and federal regulations. The LCRA acts as a primary liaison between Field Based CRAs and the Clinical Trial ...

    9. 98189 – Trial Master File / Investigator Site File Specialist

      Minimum Requirements:  ·        TMF/ISF Resource:·        Trial Master File resource who has strong experience with Investigator Site Files·        May have worked at a site and directly managed documents in the ISF·        Can also have sponsor experience building the ISF·        3-4 years of experience working with ISFs·        Bachelor’s degree·        Able to work on-site.·        Proven ...

    10. Laboratory Technician (Food & Bevg)

      Lab Tech II (Food & Bevg) Contract 4 months, PR $12-14/hr Valhalla, NY Industry: Beverage production Dept: R&D Bev Tech Apps Bev AppsTo execute and properly document product formulation work, support New Product Beverage development and commercialization within the Global Technology Applications Group.-Provide product formulation support by accurately preparing laboratory beverages -Maintain ...

    11. Lead clinical research asocciate

      ~~DUTIES – RESPONSIBILITIES: The Lead Clinical Research Associate (LCRA) is responsible for the performance of assigned Field Based Clinical Research Associates (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and federal regulations. The LCRA acts as a primary liaison between Field Based CRAs and the Clinical Trial ...

    12. Quality Engineer

      Hello,   My name is Donald Vernon and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Quality Engineer for a prominent client of ours.  This position is located in Tarrytown, NY. Details for the position are as follows:   Job Description: Evaluate safety complaint escalations and make decisions on MDR reporting, fully documenting those ...

    13. Biotech Project Manager

       My biotech client is actively seeking a Project Manager to oversee a major partnership with a high-profile client.  The ideal candidate will have a strong scientific background & take on the following tasks: Liaise with internal scientists and external client Manage project team meeting logistics and facilitation, issue resolution and scheduling, agendas and minutes Create and maintain ...

    14. SR. MANAGER, CLINICAL COMPLIANCE -NY ( CONTRACTOR)

        Within the Clinical Compliance team, this position will provide guidance and support to the clinical study teams in facilitating the Clinical Study Quality Check (CSQC), Quality Assurance Audit Responses (sites/vendors/processes), assisting responsible parties to address concerns of Suspected Serious NonCompliance, correction and prevention of potential GCP Compliance issues at ...

    15. REGULATORY DOC ASSOCIATE- NY ( CONTRACT )

        Responsible for formatting and publishing electronic documents for Regulatory submission deliverables such as INDs, IND amendments, BLAs, BLA supplements, MAAs, MAA variations in accordance with applicable Regulatory Agency regulations, guidelines, and/or specifications (eg, FDA, EMA, ICH, etc). Responsibilities: •   Formats and publishes electronic Regulatory submission documents and ...

    16. PREDICTIVE MEDICINE MANAGER - NY-CONTRACT

       This position within Predictive Medicine department (dotted-line reporting to Legal) requires a self-motivated individual with experience in coordinating multiple projects to operationally support acquisition and management of clinical samples for genomics and other exploratory biomarker studies.  Primary objective is to facilitate standardization  and  implementation of Informed Consent ...

    17. COORD CLINICAL COMPLIANCE TRAINING - NY( CONTRACT)

        This position is responsible for the coordination of the CDRA / Fellowship on-boarding program supported from within the Clinical Compliance and Training department. This also includes collating metrics and evaluation data, as well as collaborating cross-funcationally. Responsibilities: • Assist Clinical Compliance Dept to develop training and performance support tools necessary for on ...

    18. Biotech Project Manager

       My biotech client is actively seeking a Project Manager to oversee a major partnership with a high-profile client.  The ideal candidate will take on the following tasks: Liaise with internal scientists and external client Manage project team meeting logistics and facilitation, issue resolution and scheduling, agendas and minutes Create and maintain project plans and budget through ...

    19. Remote based Molecular/Cytogenetic Lab Director

      NEW Remote based Molecular/Cytogenetic Lab Director job opportunity available in CT (ABMG/NYSCoQ required and US Citizenship). If interested, please send me your resume/referral info. See brief additional info below: Job Summary: This position is responsible for analysis and reporting activities for CLIA tests. The Associate Laboratory Director should have in-depth knowledge of molecular ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    20. Biomarker Scientist

      Sigma Bullhorn ID: 7708 Location: New Haven Area, CT Position/Role: Biomarker Scientist Client Industry: Biotechnology/Pharmaceuticals Classification: 1 Year Contract (Extension Likely Into Second Half of 2016 or Conversion to FTP Status)   PLEASE NOTE: Remote Work is NOT allowed. On-Site Only. If you have any questions, I’ll be happy to answer them, but I’ll need to see a copy of your ...

    21. Clinical Lab Scientist

      Responsible for general laboratory and operational support. Including providing logistical support for samples and compounds management, ordering supplies and carrying out general bench work activities Develop, optimize, validate, and perform biomarker assays to support clinical studies Experience with ELISAs, immunoassays, LC/MS/MS, and/or flow cytometry desired Experience with ...

    22. Scientist 3

      PDS Tech is seeking a Scientist 3 for an open position in Tarrytown, NY.In  your role, you will: Provide support to the clinical affairs staff by monitoring data and ensuring clinical study documentation is complete.Report to a manager and work closely with clinical group to place orders with internal and external vendors for clinical studies, including samples.Provide support in preparing ...

    23. Scientist 1

      PDS is seekinga Scientist 1 for an open position in Tarrytown, NY.In your role, you will: Understand the Assay architecture for competitive and sandwich assays.Provide assistance in research, analysis, and experimentation for product and process development of immunoassays.Assist with assay verification/validation following protocols.Prepare computer generated verification/validation ...

    24. Global Document Specialist

      Minimum Requirements: CTMF expert (clinical trial master file) with global and domestic data Proven ability to follow SOPS from home Experience preparing Financial Disclosure and Certification documentation for FDA Submissions Job Description: Global Document Specialist (GDS) Responsibilities Performs quality control of clinical trial master file across US region and ensures ...