Advarra is seeking a TEMP Research Consultant to support the Institutional Review Board (IRB) services, enhancing research effectiveness and study start-up timelines. The role involves familiarity with Advarra’s Clinical Trial Management Software (CTMS) and the CIRBI software tool. Responsibilities include supporting Client Services teams, monitoring customer escalations, documenting issues, and participating in team meetings.
Key Responsibilities:
- Develop familiarity with Advarra’s CTMS, IRB, and CIRBI to support Client Services.
- Manage translation, safety reporting, ongoing reviews, site termination, and IRB submissions.
- Document and address customer issues promptly to ensure study start-up efficiency.
- Collaborate with the reporting manager to meet daily/weekly quality and productivity metrics.
- Utilize internal case management and reporting software for tracking and completing assignments.
- Contribute to team meetings and discussions on customer cases or protocols.
Basic Qualifications:
- Knowledge of clinical research methodology, industry regulations, study start-up activities, and Good Clinical Practice (GCP) guidelines.
- Ability to work independently and in a team environment.
- Strong organizational and administrative skills.
- Proficiency in MS Office and business software.
Preferred Qualifications:
- 0-1 year internship experience in clinical trial coordination, study start-up, regulatory affairs, IRB submissions, clinical data management, or records management.
- Excellent communication skills (written and spoken).
- High energy, proactive attitude, and ability to work in a culturally diverse environment.
- Passion for outstanding customer support with a solutions-oriented approach.
Physical and Mental Requirements:
- Ability to sit or stand for extended periods at a workstation.
- Regularly carry, raise, and lower objects up to 10 lbs.
- Focus on tasks and comprehend instructions.
- Strong verbal communication, listening, and understanding skills.
