Clinical Research Assistant

Reva Medical LLC
  • San Diego, CA
  • $2–$3 Per Hour
  • Full-time
  • Quick Apply
Today

Job Description

Summary of Essential Duties and ResponsibilitiesThe primary function in this position will be to provide departmental administrative support in the area of Clinical Affairs, including: Perform quality checks, uploads and tracking of required regulatory documents to populate the electronic Trial Master File (TMF) for designated studies. Generate reports of missing documents and upcoming expiration dates. Communicate with sites and/or study team to obtain required documents. Ensure the TMF is audit-ready in support of regulatory filings.Obtain safety-related source documents and images from clinical sites in preparation for Clinical Event Committee and Data Safety Monitoring Board meeting packages. Work with translation vendors as needed.Track device inventory and prepare shipments to sites, ensuring device integrity is maintained (i.e., temperature control and expiration dates). Process returned/expired devices.Assist with the distribution and tracking of clinical study supplies to Contract Research Organizations (CROs) and clinical centers (e.g. study binders, case report form worksheets, study devices and misc. materials)Interface with CROs to obtain study-related documentation and follow up on action itemsAssist with site invoicing and payment trackingAssist with organization and filing of study related materialsAssist in the organization and execution of Investigator meetingsProvide general administrative support as needed Education and/or ExperienceUndergraduate degree2-3 years of relevant clinical trial experience Required Knowledge/SkillsMinimum of 1-2 years of clinical study electronic Trial Master File experienceProficient with basic computer programs such as Microsoft Word, Excel PowerPoint and Adobe AcrobatDetail oriented in document review and error checkingEffective communication skills Desired Knowledge/SkillsMinimum of 1-2 years of Sponsor or CRO experienceWorking knowledge of CDISC TMF Reference Model Physical Demands/Working EnvironmentThe physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.While performing the duties of this job, the employee is frequently required to sit or stand for prolonged periods of time, frequently in front of a computer.  

Numbers & Facts

LocationSan Diego, CA
Job TypeFull-time
Salary$2–$3 Per Hour

Skills

  • Administrative Skillsunmatched
  • Adobe Product Familyunmatched
  • Billingunmatched
  • Board Meetingunmatched
  • Case Report Form (CRF)unmatched
  • Clinical Data Interchange Standards Consortium (CDISC)unmatched
  • Clinical Researchunmatched
  • Clinical Trialunmatched
  • Communication Skillsunmatched
  • Contract Research Organization (CRO)unmatched
  • Document Imagingunmatched
  • Documentationunmatched
  • Documentation Reviewunmatched
  • Medical Productsunmatched
  • Microsoft Excelunmatched
  • Microsoft PowerPointunmatched
  • Microsoft Wordunmatched
  • Physical Demandsunmatched
  • Regulationsunmatched
  • Regulatory Submissionsunmatched
  • Returns Processingunmatched

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