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clinical research in San Diego

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  1. $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 / Monitors ...

  2. Clinical Research Coordinator: Job: 1174

    Seeking to hire a: Clinical Research Study Site Coordinator Clinical Research Assistant Study Site Coordinator Overview: The Research Coordinator I oversees and administers research study and associated activities. Assists in project planning, and ensures that pre-established work scope, study protocol and regulatory requirements are followed. May recruit and coordinate research subjects, as appropriate, and serves as principle administration liaison for the project. Oversees and coordinates the ...

  3. Phlebotomy and Clinical Lab Tech: Job 1176

    Overview: The Clinical/Phlebotomy Laboratory Technician will provide technical knowledge and expertise in clinical laboratory analysis by assisting with bench top experiments, preparing and assisting with the experiments, collecting and analyzing data, and preparing reports.   This is a contract solicitation Full Time and Part Time positions available Located in San Diego, CA Qualifications:  • MLT degree, if less than 2 years of experience; or 2 or more years of experience in clinical quality ...

  4. Syringe Prepaer: Job 1182

    Overview: Shall provide research services and support compatible with the study operating capacity and equipment and will provide assistance to the Clinical Research Study Site Coordinator, Principal Investigator(s) (PI), and other assigned study personnel to facilitate biomedical human research protocols Qualifications: • Currently licensed Registered Nurse (RN) or Registered Pharmacist in California with a minimum of two years experience; one year of clinical research experience within the past ...

  5. Vaccinator: Job 1181

    This position is Part-Time This is a contract solicitation position For further details regarding the position, you will be redirected to the main career site to apply • Currently licensed Registered Nurse (RN) in California with a minimum of two years clinical experience; one year of clinical research experience within the past three years • Experience with syringe quality control procedures, pulmonary function tests, and • Knowledge of proper administration of metered vaccination doses and ...

  6. Senior Medical Science Liaison - MSL

    MUST LIVE IN CALIFORNIA OR NEVADA   We currently have an opening for Medical Science Liaison in the West Coast(territory: California, Nevada, Utah, Oregon, Washington & Hawaii). The Medical Science Liaison will function as a medical and scientific expert in Dermatology, and interact with healthcare decision makers to communicate and advance the scientific platform in alignment with goals and objectives. Responsible for engaging with Key Opinion Leaders, HCPs, institutions and other organizations ...

  7. Clinical Project Manager

    Clinical Project Manager - Contract Substantial experience in clinical research including relevant experience as a team Leader in Clinical functions or proven experience in coordinating clinical trials. Relevant Work experience in clinical research. Experience in Coordination of Clinical Trials – Preferably relevant working experience as an Associate Clinical Operations Leader or proven experience in a similar role. Individuals should have a strong understanding of the cross functional activities. ...

  8. Director Clinical Operations

    A dynamic and growing CRO is looking for a Director of Clinical Operations for their San Diego Office. This person will: • Manage clinical operations staff. • Provide strategic oversight to assigned project teams. • Support business development. • Conduct resource management and utilization as well as performance management for Clinical Operations. • Develop and implement departmental strategies, goals and objectives. Minimum Job Requirements: • BA/BS in a Life Science; MS preferred. • Minimum ...

  9. Senior Clinical Research Associate

    A dynamic and growing CRO is looking for a regional CRA. Responsibilities include but are not limited to: performing monitoring visits including site qualification, initiation, monitoring and close-out visits; maintaining regular contact with study site to ensure protocol/GCP compliance; participating in Investigator meetings and other study training meetings as required; preparing for and participating in Sponsor and FDA audits. Required qualifications: Proven success in monitoring clinical ...

  10. Senior Clinical Project Manager

    Note: Candidates must possess Ph. 1 and 2 Full Service Oncology PM Experience ~~SUMMARY: The Clinical Operations Senior Project Manager (SPM) is responsible for overall management of all phases of clinical trials, from start-up through completion of activities, utilizing MedSource or sponsor Standard Operating Procedures (as applicable), FDA regulations, and ICH-GCP guidelines. In-depth knowledge and experience of the drug development process is required, including study initiation, clinical ...

  11. Clinical Research Coordinator

    Qualifications: - At least 1 year of experience with exposure to Clinical Research. - Experience with site identification. - Experience with ICF Customization. - Experience with ICH/GCP knowledge preferred. - Strong communication skills and professionalism. - Ability to work independently. Job Description: - 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 ...

  12. Director of Biology

      The Molecular Therapeutics Department (MTD) at Nitto Denko Technical Corporation is seeking a candidate for the position of Director to head biology group in their drug product development. The Director will be responsible for leading biological activities in support of R&D through Phase 1 and Phase 2, and will work closely with internal Research and Development teams as well as with external partners and contract organizations. Requirement: PhD in cell biology, molecular biology, or related ...