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medical interpreter in San Francisco Bay Area

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  1. Stock Plan Administrator at Fluidigm

    We make biotech tools that enable our customers and ourselves to seek truth in applied life sciences. The right job isn’t about location or benefits or...

  2. Clinical Genomics Scientist, AncestryHealth at Ancestry

    In Computational Biology, Genetics, Statistics, Computer Science (or a related field). Ancestry is an Equal Opportunity Employer that makes employment decisions...

  3. Modeler (Structural Engineering, Mathematical Modeling) at Risk Management Solutions (RMS)

    The Model Development group is looking for a Modeler to help it build industry leading stochastic catastrophe models for the quantification and management of

  4. Senior Data Engineer, Bidding at Marin Software

    Statistical Programming (Matlab, R, Python). We enjoy intense mathematics and computer science challenges and approach these problems with creativity and...

  5. Lead Catastrophe Modeler (Mathematical Modeling, Catastrophe Modeling, GIS) at Risk Management Solutions (RMS)

    C#, Java, R, Python. In an engineering or science related field including but not limited to:. Civil, structural or earthquake engineering, statistics and...

    Ads
    1. Associate Director, Medical Communications Full time 2015-1329

      Description:Key member of the global medical affairs team, providing leadership and management of the publication management team and assist with providing oversight to the staff to ensure high quality managed medical communication programs with the appropriate utilization of resources.Has administrative and functional oversight of the responsibilities of employees in medical communications ...

    1. Marketing Manager at Nevro

      3-8 years of post-MBA experience in medical device or biotech marketing, or 12+ years of medical device or biotech marketing....

    1. Senior Contract Study Clinician (Non-Oncology)

      Our client Pfizer is seeking a candidate to fulfill the duties outlined below. This is a fulltime (40 hr per/wk) 1 year contract with the possibility of extension.The Non-MD/Study Clinician integrates scientific drug development knowledge to ensure excellence in development and translation of clinical research plans into efficiently delivered studies.• The Non-MD/Study Clinician is ...

    1. Principal Scientist II at Planet Pharma

      Comfortable writing code in R (including familiarity with Bioconductor packages), or other scripting languages such as Python....

    1. Contract Study Clinician

      Our client Pfizer is seeking a candidate to fulfill the duties outlined below.  This is a full-time(40 hr per/wk) 1 year contract position. Need to see work experience as a clinician or clinical scientist. Looking for at least 10 years in the industry. Located in SSF with ability to travel (minimal domestic travel) and work at the office 40 hours per week. Training, Education, and Experience ...

    1. Principal Scientist II, Bioinformatics, Sequencing at Roche

      Possess an advanced degree in computer science, bioinformatics, computational biology or related quantitative discipline (Ph.D....

    1. Study Clinician

      The Non-MD/Study Clinician integrates scientific drug development knowledge to ensure excellence in development and translation of clinical research plans into efficiently delivered studies. • The Non-MD/Study Clinician is responsible for working collaboratively with the clinical leader, physician and members of the development team to establish the Clinical Development Plans for one or more ...

    1. Administrative Assistant and Receptionist at Heron Therapeutics

      Responsible for performing a set of highly diverse administrative duties in support of a busy and growing Biotech company....

    1. Medical Information Scientist

      Education: Doctor of Pharmacy (Pharm.D.)Pharmacy Residency training a plus (e.g., Clinical, Drug Information, Managed Care)Skills: 1-3 years clinical pharmacy or equivalent experience1-3 years drug information and/or medical writing experiencePrevious relevant industry work experience, managed care experience strongly preferredMust demonstrate a high level of proficiency with Microsoft Word, ...

    1. Director Project Management at Fresenius Medical Care

      Proven experience in R & D environment. 7 years minimum project management experience in a matrixed organization, preferably in the medical device industry....

    1. Medical Writer- 2015-1254

      Description:Responsible for writing, editing, and/or reviewing clinical/regulatory documents.Creates documents that effectively and clearly convey scientific data, ensuring that such documents comply with regulatory guidelines in terms of content, structure, and style.Prepare protocols, clinical study reports, integrated summaries, Investigator's Brochures, briefing packages, end of phase 2 ...

    1. Manufacturing Associate II-Purification at Real Staffing

      Small-medium sized biotech working on one-of-kind product and technology. We are looking for an entry level professional who has at least three years of...

    1. Managed Care Medical Communication Specialist

      Kelly Scientific Resources is the world's most recognized brand in Scientific Staffing with more than 100 locations in the North America, Europe and the Pacific Rim. Our scientists contribute to the research and development of products that are used daily in the home, such as medical devices or pharmaceutical products. We employ more than 700 clinical research professionals and 4,500 ...

    1. Customer Care Specialist at InVitae

      Physicians, clinics, medical staff and patients. Catalyze scientific and medical research, and contribute to improved outcomes for everyone....

    1. Medical Writer- Full time (San Francisco Bay area) - 2015-1254

      Description:Responsible for writing, editing, and/or reviewing clinical/regulatory documents.Creates documents that effectively and clearly convey scientific data, ensuring that such documents comply with regulatory guidelines in terms of content, structure, and style.Prepare protocols, clinical study reports, integrated summaries, Investigator's Brochures, briefing packages, end of phase 2 ...

    1. Accountant I at Radiometer

      Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide....

    1. Product Safety Manager / Sr. Manager & Medical Writer (430267)

      OVERVIEW Ensure compliance with regulations for the collection and reporting of adverse events to regulatory agencies.  Review and interpret clinical data, write, edit, compile and QC documents, ensuring accuracy and quality of written deliverables with regulatory standards. Primary Responsibilities: Product Safety: •    Develop and maintain Drug Safety database. •    Provide user training ...

    1. Client Services Specialist at Invitae

      Physicians, clinics, medical staff and patients. The Client Services team is responsible for ensuring high customer satisfaction across our customer base,...

    1. Manufacturing Technician

      The Manufacturing Technician will work in a team environment, following established protocols and processes according to current industry standards. Must have ability to complete activities in accordance with Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), as well as any applicable federal regulations or Industry standards. ...

    1. Project Support Coordinator, BRM Project Support at Planet Pharma

      BS or MS in scientific, medical or healthcare subject. Project Support Coordinator, BRM Project Support....

    1. Drug Safety Associate III (Major Pharmaceuticals)

      A Drug Safety Associate (DSA), known also in the industry as a Pharmacovigilance Officer, is a health science professional responsible for the monitoring, data collection and analysis, and reporting of drug safety information for compliance with drug safety regulations in the U.S. and international markets.   LOCAL CANDIDATE PREFERRED !!!!! Palo Alto, CA Drug Safety Associate III Contract ...

    2. Drug Safety Associate II - Pharmaceuticals

        A Drug Safety Associate (DSA), known also in the industry as a Pharmacovigilance Officer, is a health science professional responsible for the monitoring, data collection and analysis, and reporting of drug safety information for compliance with drug safety regulations in the U.S. and international markets.   LOCAL CANDIDATE PREFERED !!!!!!!!!!!!! Palo Alto, CA Drug Safety Associate II ...

    3. Device Development Engineer

      Duties: **The Engineer will be responsible for change record implementation to support PTD Device Development Laboratory Testing for a 8 week period.**   Change Record Execution for Device Development   Performs dimensional inspection of laboratory test fixtures Creates engineering drawings for laboratory test fixtures, in compliance with recognized ASME standards Revises test methods, ...

    4. Drug Safety Associate III (Contract Position)

        Title :  Drug Safety Associate III Location :  Palo Alto, CA Contract (40 hours) – Contract Position  Rate : Negotiable.   The DSA III is someone who is an HCP (RN, PharmD, or MD) who has significant drug safety operations experience who can triage cases for seriousness and reportability. DESCRIPTION As a member of the Drug Safety and Pharmacovigilance department, the Drug Safety ...

    5. Manufacturing Technician

      The Manufacturing Technician will work in a team environment, following established protocols and processes according to current industry standards. Must have ability to complete activities in accordance with Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), as well as any applicable federal regulations or Industry standards. ...

      1. Principal Engineer Bioanalytical Technologies at BAYER

        Broad understanding of biotech manufacturing processes (mammalian cell culture, protein purification, fill/finish processes, process monitoring/control);...

      2. Bookkeeper/Administrative Assistant at MCLAB

        MCLAB (Molecular Cloning Laboratories), a South San Francisco-based biotech company, is a leader in DNA sequencing services and consumables....

      3. Senior Software Engineer, Java Back End (Vault) at Veeva Systems

        The cloud and life sciences.". We build innovative SaaS solutions that include CRM, content management and customer master data management for life sciences...

      4. Bioinformatics Scientist II at Genomic Health

        In Bioinformatics, Computer Science, Statistics, or a related technical field. As a key member of the R&D team this individual will collaborate with Platform...

      5. Corporate Paralegal at Avalanche Biotech

        At least 5 years of relevant experience in securities or general corporate legal matters preferably in-house in a start-up or biotech company....