Medical Assistant - Clinical Trials

CenExel

Garden Grove, CAFull-time

Behavioral Health Market Context

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Benefits

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full-time employees after 30 days of employment, including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401kHourly Range: $22.00 - $23.00/hr (Depending on education, experience, and skillset)Schedule: Full-Time - Monday - Friday 40 Hours a week - 8:00 am - 4:30 pm

Qualifications

  • Medical Assistant Certification (Required)
  • Phlebotomy and ECG experience (Required)
  • Interest in and knowledge of specific study indications
  • Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.)
  • Skilled in organization and record maintenance
  • Skilled in developing and maintaining effective working relationships with supervisors and co-workers
  • Strong personal initiative and attention to detail
  • Ability to react calmly and effectively in emergencies
  • Ability to interpret, adapt, and apply guidelines and procedures
  • Ability to clearly communicate both orally and verbally
  • 7 more items(s)

Responsibilities

  • 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
  • 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, including but not limited to, blood pressure, urine collection
  • 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
  • Essential physical requirements include sitting, typing, standing, and walking
  • Lightly active position, occasional lifting of up to 20 pounds
  • Reporting to work, as scheduled, is essential
  • 12 more items(s)


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