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clinical research in San Diego

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  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. $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 / ...

  5. 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 ...

  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. 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 ...

  8. 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, ...

  9. Director or Vice President of Scientific Affairs

    Position, Location The Director or Vice President of Scientific Affairs will lead the company’s strategic efforts in developing novel therapeutics in both cardiovascular and cancer fields through internal development and external scientific collaborations. The position is located at Zensun USA, Inc. in San Diego and needs actively working with the teams in the Company Headquarters in Shanghai, China. Specific Responsibilities  Design and execute a comprehensive plan of scientific / clinical ...