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clinical research in Los Angeles

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  1. Remote- Associate Director Physician - Oncology

    Title: Associate Director Physician - Oncology (Remote position) Job ID: 640 Industry: Biotech/Pharmaceutical Location: Wilmington, DE - Remote Duration: 3 Months, 20 hr/week, but can expand to 40 hr/week Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details:   Clinical oncologist needed to provide medical sign off and review of materials being prepared for ASCO (American Society of Clinical Oncology) Provides medical advice within clinical research projects. ...

  2. Medical Technologist (Advia 120 hematology; Olympus AU400)

    Title: Medical Technologist Job ID: 23592 Industry: Pharma/Biotech Department: Clinical Pathology Location: Thousand Oaks, CA Duration: 6 Months Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Primary job duties • Operate and maintain the Advia 120 hematology and Olympus AU400 clinical chemistry analyzers and have responsibility for compiling and summarizing experimental data. • Process and analyze research samples and assisting with lab validation. • Track and document ...

  3. Technical Writer/Project Manager

    Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Technical Writer/Project Manager Job ID: 23575 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 17 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: Write and manage functional and cross-functional process ...

  4. Technical Writer/Project Manager

    Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Technical Writer/Project Manager Job ID: 23575 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 17 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: Write and manage functional and cross-functional process ...

  5. Regional CRA

    CRA 5 immedate positions: Los Angeles CA (2), Atlanta GE (2) and Mid West (1) Qualifications include:   Must have a home office in the metropolitan areas (relocation not offered/provided). CRAs  must have:  Oncology (Phase I-III experience will receive preference); 3-5+ years of clinical research monitoring; knowledge of GCP/ICH/FDA/EMEA and clinical trial design. Up to 70% travel Breast cancer experience for 3 of the positions is a must Note: These Regional Monitor/CRA positions are ...

  6. 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, ...

  7. Clinical Data Associate II/Clinical Data Manager

    *RELOCATION to San Francisco Bay Area/Silicon Valley Required (relocation assistance provided)* This role will immediately assume study lead data management responsibilities for 3-5 concurrent clinical trials within Oncology, Respiratory or Liver Disease, utilizing primarily the Medidata RAVE electronic data capture and management system. The selected candidate will manage trials in various stages, from planning, to set-up, conduct, closeout, and archiving, in high volume, while maintaining a high ...

  8. Clinical Research Associate (Oncology)

    Job Responsibilities: Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites for GCP compliance according to inVentiv Health SOPs and/or client guidelines Generate study specific documentation including monitoring trip reports, telephone contact reports, site correspondence and expense reports Recruit investigators for participation in clinical trials Conduct project feasibility assessments Negotiate study budgets with investigators Obtain, review for ...