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Clinical Research Associate – Monitoring & Site Visits

Job in Alameda, Alameda County, California, 94501, USA
Listing for: Payfuture Technologies
Full Time position
Listed on 2026-05-28
Job specializations:
  • Research/Development
    Clinical Research, Research Scientist
Job Description & How to Apply Below
Position: Clinical Research Associate – Monitoring & Site Visits (Travel)

Clinical Research Associate job at LS Solutions. Alameda, CA.

Title:

Clinical Research Associate
Duration: 06 Months with possible extension

Location:

Alameda, CA, 94502

Description:

Note:

Travel Requirements-20-35% anywhere in USA, whenever needed. Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions.

Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary. 3-5 Years Experience Level.

Must have "Clinical Research Monitoring" experience.
Will be performing study site visits ~ qualification visit, Introduction visit, interim monitoring visits and Close out visits.
Will be generating Monitor reports and tracking to get resolutions to any items that need attention.
Will Monitor compliance to ICH guidelines, study protocol GCP (good clinical practice), Federal regulations, and any other regulations.
Will monitor study documents including Trail Master Files.
Will perform review of clinical data study listing.
Will report to management and escalate any items needed.
Will account for devices during study.
Prefer medical device background but will accept Pharma

~ Top

Skills:

1) Monitoring exp.
2) great attention to detail and good organizational skills
3) a PLUS is have exp. with EDC (electronic data capture) or Electronic Master Files

Employment Type:

Contractor
Salary: $  Per Hour

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Position Requirements
10+ Years work experience
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