Adecco Job - 39190537 | CareerArc
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Company: Adecco
Location: San Diego, CA
Career Level: Associate
Industries: Recruitment Agency, Staffing, Job Board


Adecco is currently assisting a local client in recruiting for Sr Staff Clinical Research Associates in the San Diego, CA areas.  These Sr Staff Clinical Research Associate positions are long term, contract opportunities. These positions would be GREAT opportunities to add to your resume.  Please contact us for more information!


Shift: Reg Shift M-F 8:00AM - 5:00PM

Sr Staff Clinical Research Associate positions require candidates to provide clinical support for diagnostic product development to achieve clearances and approvals in the US and internationally. Provides clinical trial site management and assures successful conduct of clinical studies consistent with applicable regulations, guidelines, and procedures. Reviews, assesses, and interprets data from ongoing and completed studies. Conducts clinical compliance activities. May be responsible for multiple clinical studies.

Responsibilities for these Sr Staff Clinical Research Associate positions include but are not limited to:

  • Responsible for the day to day management of clinical trial sites across multiple clinical projects.
  • Identifies and builds relationships with external clinical sites.
  • Manages multiple clinical trials in parallel including investigator selection, analysis of potential enrollment, preparation of trial related documentation (protocols, case report forms, consent documents, letters of agreement, confidentiality agreements, etc.) and organize investigator's start-up meetings.
  • Works with business development to contract external sites, as required.
  • Submits protocols and other documents to Institutional Review Boards / Ethics
  • Committees with follow through to ensure successful outcome.
  • Monitors the assigned clinical trials following company SOPs and in accordance with GCP and all FDA and applicable international regulations concerning clinical trial activities.
  • Assists in preparation of study-specific binders, logs and forms.
  • Plans the requirements for clinical trial material, orders clinical trial material, sets up and monitors the systems whereby the clinical project coordinator can ship clinical trial material to the investigator, maintains procedures to account for the clinical trial material, checks the expiration of clinical trial material and requests extensions if necessary.
  • Manages enrollment strategies to meet study requirements (e.g., investigator and study coordinator meetings, newsletters, advertising, etc.).
  • Coordinates shipment of clinical samples and the resulting data when central laboratory facilities are used.
  • Completed CRFs and sets up systems whereby completed CRFs are rapidly entered into the database.
  • Ensures that queries generated during data cleaning are responded to in a timely fashion.
  • Evaluates clinical data/information and prepares reports as required.
  • Participates in conference calls and meetings to review progress of ongoing clinical trials.
  • Reviews all UADEs, ensures appropriate approvals are obtained, that sites are notified and that all company procedures are complied with.
  • Project files including: ethics committee approvals; curricula vitae of investigators and study personnel; package insert and user guides; protocols; case report forms instructions; consent documents; clinical trial material shipping orders; start-up meeting attendance documentation; letters of agreement; lab reference ranges; all investigator and site correspondence; and schedules of payment.
  • Participates in the conduct of internal and external audits and inspections of clinical studies.
  • Participates in departmental planning sessions, and SOP development
  • Mentors junior CRAs to promote departmental skill base.
  • Candidates must meet the following requirements to be considered for these Sr Staff Clinical Research Associate positions:

  • Industry experience within in-vitro diagnostics highly preferred; pharmaceutical, biologics or medical device experience can substitute in part for IVD experience.
  • Thorough knowledge of GCP, ICH guidelines and other US and international clinical regulatory requirements.
  • Demonstrated ability to work independently with new, complex technologies and produce professional work products.
  • Strong written and verbal communication skills; demonstrated ability to organize and present scientific information (e.g., clinical study results) to internal and external audiences.
  • Familiarity and ability to work with office automation programs and corporate database tools.
  • Strong work ethic and demonstrated ability to deliver assignments on time.
  • What's in this for you? 

  • Weekly Pay – you receive a paycheck every week
  • Comprehensive benefits – medical, dental, vision, options available
  • Click on “Apply Now” to be considered for these REMOTE Sr Staff Clinical Research Associate positions in the San Diego, CA Area!

    Equal Opportunity Employer/Veterans/Disabled

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    The Company will consider qualified applicants with arrest and conviction records

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