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drug safety in San Francisco Bay Area

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  1. Product Transfer Scientist at Fluidigm

    We make biotech tools that enable our customers and ourselves to seek truth in applied life sciences. A minimum of 2-3 years (with PhD) or 5-6 years (with MS)...

  2. Senior Software Engineer, Java (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...

  3. Medical Director at Ascend Clinical

    Through our comprehensive test menu and our competitive technical-only program, we provide our customers and patients with accurate results, patient safety,...

  4. Field Service Coordinator at Technical Safety Services

    Knowledge of the biotech industry. Growth has hastened Technical Safety Services (TSS) need for field service coordinators....

  5. Big Data Engineer/ Senior Data Engineer at Ancestry

    Experience with R and/or MatLab. Big Data team is looking for an experienced Data Engineer who has a passion to build data products and data systems....

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    1. Manufacturing Engineer

       Purpose:  A member of the Process Engineering Team engaged in supporting efficiency improvement of all manufacturing processes and providing technical support to the Manufacturing Team.  The candidate who fills this position will be instrumental in the characterization, optimization deployment, and troubleshooting of the manufacturing processes for a components of pulmonary drug products. ...

    1. Research Associate I at Comparative Biosciences, Inc

      0-5 years’ experience working in a pharmaceutical, biotech or Contract Research Organization (CRO), preferably in pre-clinical development....

    1. 100002 - Country Studies Manager

      Minimum REQUIREMENTS:  Education and Experience: Bachelor degree in a medical/science-related field with 5 years proven experience in Clinical Research/Development or related industrySkills:·        Demonstrated ability to interact with different professional levels of the research community·        Strong leadership skills developed through leading multi-functional matrix study teams through ...

    1. Senior Writer and Content Strategist 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...

    1. EH&S Engineer

      This position will have primary responsibilities for environmental, health and safety compliance programs at L-3 Communications, Electron Devices Division located in San Carlos, CA. Responsibilities include the implementation and administration of environmental, health and safety programs ensuring compliance with Federal, State and local EH&S regulations. The focus of this position will be ...

    1. Director/ Practice Head - Information Security Services Consulting at Trianz

      Seeing our talent d evelop into leaders- is what’s fundamental for everyone at Trianz. Ou r c lients are transforming their businesses, competitive strategies,...

    1. Medical Director - Medical Affairs - Rheumatic Disease - San Jose, CA

      Seeking innovative Medical Affairs leader with proven success leading Medical Affairs activities for therapeutics treating Rheumatic diseases or similar autoimmune disorders causing painful skin, joint, and connective tissue inflammation. *** Develop and execute plans to inform and educate KOLs, healthcare professionals, physicians, providers, prescribers, payors, and patient ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Principal Data Scientist at AT&T

      Masters of Science or PhD in Computer Science, Math or Scientific Computing; Experience with Linux, Hadoop/Pig/Hive, Python and/or R, data mining and machine...

    1. Medical Director - Rheumatology Drug Clinical Development

      Seeking individual who can manage clinical trials in phases I through III for new new drugs aimed at treating autoimmune disorders: Lupus, Rheumatoid Arthritis, Psoriatic Arthritis, or similar affecting the skin, joints, and connective tissues. Shall: *** Lead all major Clinical Development activities during early Phase I through late Phase III. *** Oversee the design, development, ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Sr. Research Scientist Level - Process Chemistry Req #31445 at Gilead

      Gilead Sciences, Inc. People, a pipeline of late-stage drug candidates, and unmatched patient access. Responsible for developing chemical processes for the...

    1. Director - Clinical Development - Skin & Joint Inflammation

      Seeking MD with Clinical Development and medical leadership experience who can lead clinical trials for new drugs aimed at treating autoimmune disorders causing inflammation of the skin, joints, and connective tissues. Shall: *** Manage all efforts involved in the design and execution of multiple ongoing clinical studies in Phase I through III. *** Write clinical sections of regulatory ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Sr. Research Scientist Level - Process Chemistry Req #31445 at Gilead Sciences

      Gilead Sciences, Inc. People, a pipeline of late-stage drug candidates, and unmatched patient access. Responsible for developing chemical processes for the...

    1. Oncologist - Medical Affairs Director - Immunotherapies

      Seeking experience leading Medical Affairs programs for therapeutics advancing from late-stage clinical development through approval and launch. Must have oncology drug trial or medical affairs expertise and MD, DO, or equivalent. Must demonstrate: *** Experience leading Medical Affairs programs for novel drugs transitioning from clinical trials in Phase III to launch. *** Ability and ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Sr IT R&D Business Analyst- Full time Opportunity- Sunnyvale, CA at Park computer systems

      Strong knowledge of *processes and applications related to Clinical Operations, Medical Affairs, Clinical Data Management, Clinical Science, Biostatistics, and...

    1. Clinical Trial Associate - 99099

      Minimum Requirements:Education and Knowledge:University Degree or Equivalent preferably in a medical/science-related field Prior work experience demonstrating knowledge and understanding of clinical trials Previous experience managing projects is desirableExperience, Skills and Competencies:Experience working as part of a team with a proven ability to make an active contribution to the team's ...

    1. Client Experience Manager at Exhibit/Event Flooring Company

      P R I M A R Y D A Y T O D A Y R E S P O N S I B I L I T I E S*. O R G A N I Z A T I O N S T R U C T U R E*. Client Experience Manager....

    1. Clinical Drug Safety Associate I/II

      inVentiv Health – Transforming Promising Ideas into Commercial RealityJob Title: Safety Associate I/IILocation: Cherry Hill, NJ – OR – San Francisco, CAPrimary Function: The Safety Associate I is responsible for the processing of adverse event reports and product quality complaints information received from sites and reporters.Job Description:· Complete data entry in safety database including ...

    1. Senior State Content Editor, Commercial Transactions (California) at Thomson Reuters

      Consumer regulatory issues (product safety and labeling). We deliver this must-have insight to the financial and risk, legal, tax and accounting, intellectual...

    1. Senior Director, Global Pharmacovigilance

      Summary:This position is responsible to serve as the Head of Pharmacovigilance and provide Pharmacovigilance leadership for all investigational and commercial products. This includes assuring the timely and accurate collection, review, and analysis of Serious Adverse Events (SAE) reports and safety reporting compliance. This person will oversee implementation and maintenance of the Safety ...

    1. Software Development Engineer in Test (Android & IoT) Big Data at AT&T

      BS in Computer Science / Engineering or equivalent experience. R knowledge and general big data experience is a plus....

    1. Sr. Manager/Associate Director Medical Affairs

      DescriptionThe Regulatory Affairs Sr. Manager/Associate Director will be responsible for maintaining collaborative relations and efficient communications with health authorities and for providing regulatory guidance to a cross functional team and managing a group of regulatory professionals during preparation and submission of regulatory documents. This position will report to the Sr. ...

    2. System Verification Specialist II

      This is a 1 Year AssignmentPay Rate: $35.00 Hourly**Candidates must complete background and drug screenings prior to start.Participates in system verification testing for complex medical diagnostic products and systems. The systems generally include a combination of hardware, reagents and software components and can be part of an upgrade or option to an existing system.Applies acquired job ...

    3. Sr. Biostatistician

      Essential Duties and Job Functions : Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting.Provides statistical consultation on trial design and study ...

    4. Mechanical Inspector

      This is a 1 Year Contract AssignmentPay Rate: $20.00 HourlySan Jose, CACandidates must complete background and drug screenings prior to start.A minimum of a High School Diploma/GED2 - 3 years visual and mechanical inspection experience.Experience in the use of & programming inspection measuring tools including Zeiss CMM.A minimum of 6 months working in a regulated manufacturing environment ...

    5. Research Associate

      Duties: A temp position in the In Vivo Studies Group in Safety Assessment. The candidate will be working as a part of a team that is responsible for the planning and execution of pre-clinical drug development studies (including pharmacokinetic and toxicology) supporting a large customer base. Responsibilities will include the following in order to support Scientific Researchers in the conduct ...

    6. Sr. Biostatistician

      Essential Duties and Job Functions : Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting.Provides statistical consultation on trial design and study ...

    7. System Verification Specialist II

      This is a 1 Year AssignmentPay Rate:  $35.00 Hourly**Candidates must complete background and drug screenings prior to start.Participates in system verification testing for complex medical diagnostic products and systems. The systems generally include a combination of hardware, reagents and software components and can be part of an upgrade or option to an existing system.Applies acquired job ...

    8. Senior Manager, Drug Safety and Pharmacovigilance

      Senior Manager, Drug Safety and PharmacovigilanceFull-time Description:A world-class global pharmaceutical company that focuses on developing and manufacturing innovative medicines is currently seeking a Senior Manager of Drug Safety and Pharmacovigilance as their company is rapidly expanding!  Now is a pivotal time to get in with this group as the Senior Manager of Drug Safety and ...

    9. Pharmaceutical Clinical Study Scientist (Contract) 1459

      Description: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 compounds from lead development in Discovery to Phase I-II clinical trials.Integrates scientific drug development knowledge to ensure translation of clinical research plans into efficiently delivered ...

    10. Sr Global Medical Affairs Director - Cancer Immunotherapies

      Seeking individual with background in cancer immunotherapies who can create and manage global medical affairs strategies for multiple high-profile drug programs. Key Activities: *** Develop and execute Medical Affairs strategies that build a bridge between the company, healthcare professionals, Key Opinion Leaders (KOLs), and patient representatives. *** Act as the key medical and ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

      1. Licensed Clinical Social Worker (Psych Emergency Dept) at Marin General Hospital

        D. Documents all collateral contracts. D. Maintains positive working relationships with community agencies. D. Participates in Quality Improvement activities...

      2. Licensed Clinical Social Worker or Clinical Social Worker (MSW) (Sign On Bonus) at Marin General Hospital

        D. Documents all collateral contracts. D. Maintains positive working relationships with community agencies. D. Participates in Quality Improvement activities...

      3. Market Planning Manager – Pharma/Biotech W2 ONLY at Consultant Specialists, Inc. (CSI)

        BS/BA with business, finance or science concentration preferred. 4597268 Market Planning Manager – Pharma/Biotech W2 ONLY 8 Month Contract....

      4. Medical Director at Alkahest, Inc.

        Relevant clinical and regulatory history of other drugs with the same or similar indications; Expertise in the areas of drug development, strategic planning,...

      5. Bio/Pharma Freelance Writer at Bulletproof Documentation, Inc.

        SOPs, Biotech, Pharmaceutical, Documentation:. Duties/Responsibilities:....