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clinical research in San Francisco Bay Area

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  1. CRA I /II – Full Time

    DESCRIPTION: Responsible for implementing and monitoring clinical trials and expands experience in clinical trial and vendor management procedures.  Works closely with study coordinators and investigators to ensure compliance with protocol and overall clinical objectives. Identifies projects/tasks and works with Clinical Trial Manager to complete.  Demonstrates ability to carry out all CRA I functions with minimal supervision.  In collaboration with manager and/or Lead CRA, maintains ...

  2. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...

  3. Physics Manager

      As Manager, Physics Research and Development you will be responsible for managing the physics team within the Research Group, with a focus on the physics-related features of the CyberKnife System. You will direct the physical investigation and development of new devices and methods for improved therapeutic radiation delivery and new Quality Assurance tools and procedures, involving treatment planning, treatment delivery, medical imaging, robotics, and radiation dosimetry. This role requires a high ...

  4. Data Implementation Manager

     ~~Job Overview Zephyr Health is a fast-growing technology company that is breaking new ground in the Life Sciences industry with innovative data visualization and analytics applications. We are looking for a Data Implementation Manager to lead the day-to-day operations of execution and implementation of our customer solutions. The role is ideal for someone who thrives in a fast-paced environment, is highly collaborative, welcomes input from all sides, and perseveres with focus on addressing client ...

  5. $5K Sign On Bonus- CRA  Monitors Needed - Set Yourself Up for Success

    CRAs - Join Covance and receive a $5000 Sign On Bonus! Meet the CRA hiring team at the ACRP conference - email [email removed].   Set yourself up for SUCCESS with Early Clinical Development! Now is the time to join our growing business where you have supportive management and a cohesive team. At Covance, you are not just a number. We value you and your hard work...we want you to succeed.   URGENT Need for Oncology Monitors!  Calling all Experienced Clinical Research Associates / CRAs / ...

  6. Senior Clinical Research Associate – Full Time Position

      Description   Responsible for implementing set-up, execution, oversight and reporting of clinical studies while ensuring that the conduct of the trial is in compliance with the protocol, ICH/GCP, and applicable regulatory requirements.   Key Accountabilities/Core Job Responsibilities: Lead multifunctional team through clinical studies activities that meet ICH/GCP and SOP requirements Develop clinical trial protocol synopsis, protocols, amendments and informed consent documents Develop ...

  7. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...

  8. Clinical Research Manager

    Job summary The Clinical Research Manager (CRM) is responsible for managing and meeting the objectives of a clinical study.  This position should be able to independently handle various clinical study protocols and assignments. The CRM duties will primarily support the daily in-house management of clinical studies; however, there will be a combination of both in-house and field responsibilities. In-house, the Clinical Research Manager will have an instrumental role in the analysis and review of ...

  9. Data Coordinator, Clinical Development

    Harvest Technical is seeking a Data Coordinator, Clinical Development for our Biotech client in the Greater Bay Area. Description: Entry of data into the Clinical Trial Management System (CTMS), including: Create and update organizations, contacts, sites and addresses Generate site numbers Enter and update site budgets Enter and update study and site milestones Coordinate the collection of information from study teams and CROs for entry into CTMS Perform CTMS data ...

  10. Clinical Data Manager

      Job Responsibilities:   Review and understanding of clinical Research documents such as Protocols, Case report forms,  RAVE reports and Statistical Analysis. Devise and Review data management plan (DMP), and update data management plan throughout life cycle of the study and ensure the DMP complies with the regulatory requirements. Design and Development of electronic case report forms by thoroughly understanding the protocol requirements and present it to the cross functional teams for the ...

  11. Director Drug Safety Science (perm)

    Looking for strong Safety Surveillance experience, must have management experience as this position will manage other staff.   Minimum REQUIREMENTS: Pharm.D., Ph.D. or M.D. Minimum of 7-10 years experience with pharmacovigilance or clinical drug safety including risk/benefit analysis and safety assessment Excellent clinical judgment and ability to communicate complex clinical issues in a scientifically sound and understandable way Must have excellent writing and communication skills ...

  12. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...

  13. Home Based Regional CRA

    Our client is currently seeking contract and permanent direct-hire Regional CRAs with a minimum of 2 years of experience in Cardiovascular studies, preferably in Myocardial Infarction and/or device.   Major Roles and Responsibilities: Demonstrates management of all clinical investigative sites according to the Federal Code of Regulations, Good Clinical Practices, ICH Guidelines, local regulations, and Clinipace SOPs and/or Sponsor SOPs. Creates quality written trip reports, tracking, and site ...

  14. Senior Clinical Research Associate

    We are currently looking to hire Permanent Regional CRAs Job Description   The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, ...

  15. Bioinformatics Scientist

    The Position We are seeking an exceptionally talented bioinformatics scientist to join our R&D team. This individual will be responsible for the design and implementation of algorithmic approaches and data management strategies empowering analysis of complex genomics data sets along with communicating results to audiences with a wide variety of technical expertise. Who You Are The successful candidate should be motivated by the opportunity to contribute to the discovery and development of ...

  16. Senior Software Developer

    The Position: As a senior member of the software development team at Veracyte you will develop and support business critical systems and software programs for commercial, lab and clinical database systems at Veracyte. This is an opportunity to use industry standard best practices to plan specifications, design and implement both internal and customer facing information systems.  The successful person in position will design, develop and configure software applications in client/server and web ...

  17. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...

  18. Principal Clinical Supply Project Manager

    Principal Clinical Supply Project Manager in Redwood City, CA. Minimum Education Requirements:   Bachelor’s Degree required, preferably in physical science, math, engineering, or pharmacy.   Minimum Experience Required:   3 - 5+ years total experience in the Pharmaceutical Industry.   Must have experience in one of the following areas:   • Drug discovery (eg, Process Chemistry, Analytical Chemistry) • Drug development (eg, Formulation) • Clinical operations (eg, Clinical Project ...

  19. Global Studies Manager

    Job Title: Global Studies Manager in South San Francisco, CA.   Main Responsibilities and Accountabilities:   - Provides direction and leadership to one or more clinical operations teams Develops operational plans including site monitoring strategies, risk mitigation strategies, trial budgets, site selection, and clinical supplies management. - Builds effective and efficient high performing operations teams and ensures team members are aware of their accountabilities, responsibilities and ...

  20. Associate Director, Clinical Data Management

    Key Responsibilities: Oversees Clinical Data Management processes, ensuring timelines and contracts are adhered to and quality standards are met.  Maintains system validation documentation and other regulatory documentation. Manages, monitors and reports on progress of Data Management projects. Responsible for resources planning and tasks assignment of direct reports.  Supports department infrastructure.  Supports department head by successfully completing ad hoc projects to improve departmental ...

  21. Clinical Research Associate – Full Time Position

      DESCRIPTION: Overview:  Ensure timely conduct of clinical studies according to protocols, Good Clinical Practice, Standard Operating Procedures and all applicable regulations governing the conduct of clinical trials. Position reports to Associate Director, Clinical Operations.   Responsibilities: In conjunction with Associate Director, coordinate activities of clinical trial sites. Attend Site Qualification Visits to assess investigator’s staff and facilities. Contribute to study design ...

  22. Clinical Research Associate - Immune Design - San Francisco

    Clinical Research Associate - San Francisco Office   Immune Design Immune Design is leveraging two powerful, versatile discovery platforms of innovative technologies that work in partnership to develop product candidates that activate, guide, and strengthen patient-specific immune responses to potentially fight cancer and other chronic diseases.  The Company was founded in 2008 with cutting edge molecular tools to shape the immune response by selectively activating and targeting dendritic cells.  ...

  23. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...

  24. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...