ICONMA, LLC Hiring for Clinical Research Assistant – Critical Need at San Diego Full Time

Job Description

• Collect project data through interviews, chart review or other methods.

• May collect, secure and assist with biospecimen management.

• Set up tracking tools, assist in develop forms and document procedures.

• Monitors and tracks study over time and provides follow-up as needed.

• Summarizes data for progress reports.

• Orient and provide training to team members and/or clinical staff on specific project tasks.

• If assigned to clinical trial, may work with monitors at clinical sites.

• Adheres to compliance and privacy/ confidentiality requirements and standards.

• Adheres to GCP and compliance regulations for clinical trials.

• Responsible for reviewing own work to ensure data quality.

• Acquires and maintains knowledge of client systems and databases.

• Identifies study issues and collaborates with team members to develop and implement solutions.

• Serves as a member on department or study-related committees.

• May assist with tracking information for invoices.

  Requirements

• Experience in Clinical Research or clinical trials.

• Must have 1+ years of experience in Clinical Research or clinical trials.

  As an equal opportunity employer, ICONMA prides itself on creating an employment environment that supports and encourages the abilities of all persons regardless of race, color, gender, age, sexual orientation, citizenship, or disability.