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clinical research in San Diego

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  1. Clinical Laboratory Scientist  (CLS)

    HRC 05-23Clinical Laboratory Scientist - CLS - San Diego  Exciting and growing diagnostics company focused on mass spectrometry based biomarker discovery. The ideal candidate will be flexible and enthusiastic and inspired by innovation.The successful candidate will be involved in very hands-on bench work, responsible for performing assay validation, CLIA testing and reporting test results.   Essential Duties will include:• Responsible for performing technical and scientific processes and procedures ...

  2. Vice President, Regulatory Affairs

    Vice President, Regulatory Affairs Summary: The Vice President, Regulatory Affairs leads the development, implementation, and direction of effective regulatory strategies with oversight for all of quality and compliance for the company's oncology pharmaceuticals. The position has responsibility for tracking and evaluating governmental and international regulations and their impact relative to drug regulation. The incumbent builds and maintains excellent relationships with the FDA, other health ...

  3. Vice President, Regulatory Affairs

    HRC 17-21Vice President, Regulatory AffairsSummary: The Vice President, Regulatory Affairs leads the development, implementation, and direction of effective regulatory strategies with oversight for all of quality and compliance for the company’s oncology pharmaceuticals. The position has responsibility for tracking and evaluating governmental and international regulations and their impact relative to drug regulation. The incumbent builds and maintains excellent relationships with the FDA, other ...

  4. Sr. Specialist/Educator Neuro/Stroke PCU in San Diego, CA

    This Sr. Specialist/Educator position will oversee staff development in the Neuro/Stroke Progressive Care Unit. Under the new Clinical Practice Model, this role will function primarily as a staff developer. The National Nursing Staff Development Model has been adopted as the theoretical foundation for this role. The Sr. Specialist will focus on the following: orientation, competency program, in-service education, continuing education, career development/role transition, research and scholarship, and ...

  5. ASSOCIATE SALES REP - STRYKER MEDICAL DEVICE

    **PLEASE DO NOT APPLY ON YOUR OWN! IF YOU DO WE CANNOT REPRESENT YOU!**   ** THIS IS AN ON-CALL POSITION!!!! READ CAREFULLY BEFORE APPLYING!!!** THANKS!    Company:  Stryker   Division: CMF- Through close collaboration with leading surgeons worldwide, Stryker Craniomaxillofacial has gained a well-earned reputation as a market leader for its innovative developments in Craniomaxillofacial and Neurosurgery. In order to maintain this spirit of innovation and leadership, we continuously focus our ...

  6. Clinical Trial Specialist (Contract)

    Clinical Trial Specialist (Contract)   Responsibilities: Conduct and facilitate specific start-up activities such as feasibility, site identification, pre-qualification, Site Regulatory Package (SRP) review and approval, Clinical Site Agreements (CSA) and Informed Consent (ICF) customization and negotiation (where required). IRB/IEC application preparation and submission, in accordance with relevant regulations, SOPs and study specific procedures.   Qualifications: Min 1 year of experience with ...

  7. Clinical Laboratory Scientist  (CLS)

    Clinical Laboratory Scientist - CLS - San DiegoExciting and growing diagnostics company focused on mass spectrometry based biomarker discovery. The ideal candidate will be flexible and enthusiastic and inspired by innovation.The successful candidate will be involved in very hands-on bench work, responsible for performing assay validation, CLIA testing and reporting test results. Essential Duties will include:• Responsible for performing technical and scientific processes and procedures in a moderate ...

  8. Contract Clinical Research Associate- Must have Endocrinology exp.

    ~~Contract Regional Clinical Research Associate – San Diego, CA area (6 month contract) Must have Endocrinology experience Description: The Clinical Research Associate manages all aspects of site monitoring responsibilities for clinical trials according to Good Clinical Practices (GCPs), company SOPs, ICH guidelines and study protocols, including pre-study, initiation, interim and closeout visits. Responsibilities:  Assists with study start-up activities.  Prepares study manuals, informed ...

  9. Clinical Trial Specialist Study Start Up

    Clinical Trial Specialist (Contract)   Responsibilities: Conduct and facilitate specific start-up activities such as feasibility, site identification, pre-qualification, Site Regulatory Package (SRP) review and approval, Clinical Site Agreements (CSA) and Informed Consent (ICF) customization and negotiation (where required). IRB/IEC application preparation and submission, in accordance with relevant regulations, SOPs and study specific procedures.   Qualifications: Min 1 year of experience with ...

  10. $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 / ...

  11. RN II - Medicine - 7p-7a-pd relo to Houston, TX-bzs1847

    RN II - Night - Medicine (Jones 10) - Full-Time Job Ref: 5053 Talent Area: RN - Medicine Area/Department: Nursing Unit-Jones 10 Employment Type: Full-Time Job Type: Regular Work Week: M - F Job Summary DUTIES AND RESPONSIBILITIES       1. LEADERSHIP a. Provides care to increasingly complex patients and coordinates the interdisciplinary team. (Quality/Safety)  b. Identifies and presents areas for improvement in patient care or unit operations and offers solutions by participating in unit projects ...

  12. Senior Medical Writer (home based)

      Regulatory Medical Writer Must have written all of the following: NDA submissions, Protocols, Narratives, Case Report Studies, and Inform Consent forms   Write clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical ...

  13. 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, ...

  14. RN II - Medicine - 7p-7a-pd relo to Houston, TX-bzs1847

    RN II - Night - Medicine (Jones 10) - Full-Time Job Ref: 5053 Talent Area: RN - Medicine Area/Department: Nursing Unit-Jones 10 Employment Type: Full-Time Job Type: Regular Work Week: M - F Job Summary DUTIES AND RESPONSIBILITIES       1. LEADERSHIP a. Provides care to increasingly complex patients and coordinates the interdisciplinary team. (Quality/Safety)  b. Identifies and presents areas for improvement in patient care or unit operations and offers solutions by participating in unit projects ...

  15. Applications Manager-paid relo to Houston, TX-bzs6223

    Job Title: Applications Manager  Location: Houston, TX     Summary:   The Applications Manager’s role is to supervise and maintain the organization’s repository of software applications through best practices and the appropriate staffing and management of a technical team. The Applications Manager is also responsible for planning and coordinating the processes required for the provision of user applications and systems necessary for business operations. This individual will apply proven communication ...

  16. IT Training Specialist-paid relo to Hillsboro, OR-bza1396

    Location: Oregon - Portland - Hillsboro (Portland Metro)  SUMMARY OF DUTIES Works with the Clinical Information Systems (CIS) to identify training needs, developing curriculum and job aids that will help staff be more efficient and productive while standardize procedures.  Works or leads project teams in developing instructional materials in all areas of information technology systems.  Participates in the design and delivery of training/orientation programs for respective solution(s) and upgraded ...

  17. Formulation Senior Associate / Formulation Development Scientist

    Formulation Senior Associate/Scientist Successful candidates will have a Bachelors or Masters degree in chemical engineering, biochemistry, pharmaceutics or related field, with a minimum of 5-7 years relevant experience. Familiarity with the pharmaceutical process and GMP operations is preferred. We are seeking self-motivated and ingenious individuals, capable of operating independently in the lab and able to create formulations and perform characterization assays to understand the physicochemical ...

  18. Senior Regional Clinical Research Associates

    Job Description: Senior Regional Clinical Research Associate-Western Region We are partnering with a top performing CRO company on a confidential search for Senior Regional Clinical Research Associates to join their expanding field monitoring team.  This role is responsible for the clinical monitoring of designated projects in accordance with applicable SOPs, ICH and GCP guidelines. Responsibilities include performing clinical on-site monitoring activities, collecting regulatory documentation, ...

  19. Medical Biller II/Project Specialist

    Our company has room to bring a Medical Biller II/Project Specialist to add to our growing team. Our company provides outsourced billing & collections services for the emergency medical transportation industry. We support our clients to improve their overall financial health of their programs. Our Mission is to provide a consistent, customer centric service for patient care through clinical research, quality improvement, and cost effectiveness. The position we are looking to add on requires a person ...

  20. Grant Writer - Medical Outpatient Clinic

    Req #:  2386 Dept:    Administration Hours:  PT (Monday through Friday, 8:00 a.m. to 12:00 p.m.) Job Summary: Responsible for successful researching, conceptualizing, developing and writing preventive, clinical, research and health promotion programs.  Responsible for working cooperatively with community and clinic staff to identify programmatic needs and models.  Strive toward collaborative efforts with multiple public and private organizations to design well being programs which will benefit the ...

  21. IT Training Specialist-paid relo to Hillsboro, OR-bzs1396SD

    Location: Oregon - Portland - Hillsboro (Portland Metro)  SUMMARY OF DUTIES Works with the Clinical Information Systems (CIS) to identify training needs, developing curriculum and job aids that will help staff be more efficient and productive while standardize procedures.  Works or leads project teams in developing instructional materials in all areas of information technology systems.  Participates in the design and delivery of training/orientation programs for respective solution(s) and upgraded ...

  22. Manager,Development - C#, .Net-paid relo to Edison, NJ-bzs7698SD

    Our company is on the cusp of explosive growth and change.  The organization is ready and hungry for talented individuals who can help us on our quest to become the best place to work in life sciences.  This takes a high energy, courageous and engaging individual that is ready to challenge and to be challenged by exceptionally bright leaders. The Center of Excellence Development Manager is responsible for hands-on tracking and managing of the delivery of specific defect solutions while working in ...

  23. Sr. Software Engineer I-paid relo to New York, NY-bzs7507SD

      The Senior Software Engineer I is responsible for hands-on development of our company's software applications. Responsibility Overview • Develop software applications and associated artifacts such as unit tests, installation programs and test automation code. • Apply good technical practices such as re-factoring, continuous integration, test automation, source code control and review. • Provide diagnostic support and bug fixing for software applications. • Provide technical guidance, ...

  24. Manager, Development  C#, .Net - paid relo to Edison, NJ - bzs7698SD

     Our company is on the cusp of explosive growth and change.  The organization is ready and hungry for talented individuals who can help us on our quest to become the best place to work in life sciences.  This takes a high energy, courageous and engaging individual that is ready to challenge and to be challenged by exceptionally bright leaders. The Center of Excellence Development Manager is responsible for hands-on tracking and managing of the delivery of specific defect solutions while working in ...