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Clinical Research Assistant (Must Live in Los Angeles and Speak Spanish)

Clinical Research Assistant (Must Live in Los Angeles and Speak Spanish)

Angel City VALos Angeles, CA, US
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Title :

  • Part time Clinical Research assistant Job Summary : The Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.

Essential Responsibilities and Duties :

  • Creating and maintaining patient charts for all assigned studies.
  • Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
  • Filing of lab results, EKG results, and other communication in designated patient charts.
  • Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
  • Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
  • Assisting Coordinators in assessments, blood pressure, urine collection, draw labs
  • Communicating with study participants, caregivers, third party vendors and laboratories as needed.
  • Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
  • Aiding Coordinators in the facilitation of study monitoring visits.
  • Completion of daily responsibilities delegated by CRC as they pertain to the study and / or participants.
  • Assumes other duties and responsibilities as assigned.

    • The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

  • Office / administrative tasks assigned ie :
  • resupplying exam rooms, ordering office supplies, answering phone calls, etc.

    • Education / Experience / Skills :

  • High school graduate or equivalent.
  • Bac
  • Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
  • Skilled in organization and record maintenance.
  • Strong personal initiative and attention to detail.
  • Ability to clearly communicate both orally and verbally.
  • Prior experience in healthcare, research, or clinical settings is a plus.
  • Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus.
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