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regulatory affairs in San Diego

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  1. Clinical Operations Manager/Line Manager at SynteractHCR, Inc.

    SynteractHCR is a midsize CRO offering customized Phase I through IV multi-therapeutic services to Pharma, Biotech and Medical Device companies....

  2. Financial Reporting Manager at Transition Staffing Group, Inc

    Experience and familiarity with technology and biotech companies and/or diagnostic product companies. We are working with a pre-IPO bio tech company seeking to...

  3. Computational Biologist at Ignyta

    Experience with statistical software, such as R, is a plus MINIMUM EDUCATION AND EXPERIENCE. Degree in Biological Sciences or related scientific discipline with...

  4. Biologist at Eli Lilly

    Bachelors degree in Biological Sciences. The successful candidate will work in a multidisciplinary team, interacting with colleagues at AME and within BioTDR to...

  5. Director - Full Service Data management at Theorem Clinical Research

    Maintains current professional knowledge in fields of information management, computer science, quality assurance, regulatory affairs, and applicable areas of...

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    1. Training / Clinical Development Manager - REMOTE- 97894

      Title of Position: Training and Development ManagerWork From Home /  RemoteJob Description:The Training and Development Mgr will be responsible for designing, developing, managing, and implementing high quality training curricula and programs for the GRAAS and CRDC organizations. The position will focus on training in the pharmacovigilance, R&D compliance, regulatory affairs, and drug safety ...

    1. Bioinformatic Research Analyst at The Samuel Roberts Noble Foundation

      Degree in computer science, electronic engineering or related bioinformatics and computational biology science field with 2 year of experience in bioinformatics...

    1. Device Project Manager

      The Device Project Manager is responsible for assisting the Vice President of Scientific Affairs in the generation of development and commercialization plans for Zensun’s medical device business.  Additional responsibilities include generating project plans and timelines, identifying and monitoring critical path items, tracking budgeted expenses, managing meetings (eg, agendas, minutes, ...

    1. Clinical Trials Assistant at Neurocrine Biosciences

      Establish collaborative relationships with colleagues in Clinical Development, Regulatory Affairs and throughout the Company....

    1. Senior Regulatory Affairs Specialist

      Simply Biotech specializes in recruiting exclusively for the biotech community. We are currently seeking a Senior Regulatory Affairs Specialist for a leading and growing biotech firm.The Senior Regulatory Affairs Specialist will work with interdepartment teams to lead and author regulatory submission initiatives and ensure that regulatory submission projects are completed on time and that ...

    1. Field Service Engineer - Ottawa at Radiometer

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

    1. Companion Diagnostic Development Director - San Diego, CA

      Newly founded biotech company seeking individual with proven success leading efforts for companion diagnostic or clinical trials in collaboration with oncology therapeutic trials. Functions: *** Create clinical trial protocols, case report forms, study reports and clinical data listing for trials. *** Oversee development and approval of biomarkers for drug efficacy and patient selection ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Data Scientist at Virtual Instruments

      MS or PhD in data mining, machine learning, statistical analysis, applied mathematics, quantitative sciences, signal/image processing or equivalent....

    1. Regulatory Lead (430488)

      **ONLY LOCAL, SOUTHERN CALIFORNIA APPLICANTS PLEASE** Job Description Create and maintain regulatory timelines and track deliverables to timelines to ensure regulatory submission timelines are met. Participate in the development of regulatory strategy and provide strategic input and regulatory advice to the project teams on development program. Proactively identify project issues and ...

    1. Research Associate II (Social Science Analyst) at JBS International, Inc.

      Knowledge of SPSS, R, Mplus, or STATA (multiple statistical software packages preferred). MA or MS degree and a minimum of 7 years of experience in social...

    1. Research Scientist at Makro Scientific

      Previous experience in pharma and/or biotech environment is preferred. B.S....

    1. Research Scientist at Scientific

      _Previous experience in pharma and/or biotech environment is preferred. Job Title Description:....

    1. Immune Assay Scientist, Vaccine Immunotherapeutics at Pfizer Inc.

      Bachelor of Science in life sciences, preferably including coursework in immunology. Subject to further legal review and statutory or regulatory clarification,...

    1. Scientist III at Dart NeuroScience LLC

      PhD in Neurobiology, Molecular Pharmacology, Cellular Biology, Electrophysiology, Enzymology or Biochemistry with proven experience of in vitro/ex vivo...

    1. Sr. Safety Lab Data Manager at Theorem Clinical Research

      Is a leading midsized provider of comprehensive clinical research and development services with offices in more than 30 countries and a customer base comprised...

      1. Temp Facilities & Material Handling Tech. Biotech/Pharma experience at Agena Bioscience

        At least 1 years working in biotech or pharma space. The Temporary Facilities and Materials Handling Technician position will provide multifunctional support...

      2. Sr Director, Global Intellectual Property at Illumina, Inc.

        Experience in a biotech or life sciences company strongly preferred; Undergraduate or advanced degree in chemistry or life sciences is required....

      3. Technical Data Visualization Programmer (Remote in US or Canada) at Theorem Clinical Research

        Computer Science background preferred. Additional background helpful – e.g. computer science degree, data management, EDC programming....

      4. Principal SAS Programmer- Full-Time Salaried (Remote in US/Canada) at Theorem Clinical Research

        Hands-on experience with CDISC/SDTM/ADaM programming, TLG, define documentation along with understanding of regulatory requirements....

      5. Micro-Cleaner for Cleanroom Environments at Controlled Contamination Services

        We are looking for strong and experienced Micro-Cleaners to hire and work on crews in Sorrento Valley and the surrounding area. This individual must have a