Research Assistant I

CenExel

Hollywood, FLFull-timePosted May 1, 2026

Behavioral Health Market Context

Latest national behavioral health workforce report (2026-W24)Florida behavioral health workforce newsBrowse all behavioral health workforce news
Apply Nowvia LinkedIn

Qualifications

  • •High school graduate or equivalent
  • •Must be able to effectively communicate verbally and in writing in English and Spanish
  • •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 emergency situations
  • •Ability to interpret, adapt and apply guidelines and procedures
  • •Ability to clearly communicate both orally and verbally
  • •Essential physical requirements include sitting, typing, standing, and walking
  • •7 more items(s)

Responsibilities

  • •With moderate oversight, 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
  • •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
  • •Conducts 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
  • •Lightly active position, occasional lifting of up to 20 pounds and/or pushing carts up to 50 pounds
  • •Reporting to work, as scheduled, is essential
  • •11 more items(s)
Apply for this Position

More Jobs