Tech Stack
Google Cloud Platform
About the role
- Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies
- Assists Clinical Monitoring staff with site management activities
- Communicating with sites to ensure compliance with protocol requirements
- Creates and assists with maintenance of project files
- Participates in file audits
- Prepares and maintains site manuals, reference tools and other documents
- Tracks incoming and outgoing clinical and regulatory documents
- Manages shared mailbox, processes site requests
- Coordinates the ordering, packaging, shipping and tracking of site supplies and materials
- Assists with coordination of team meetings, attends meetings and prepares accurate meeting minutes and action items
- Anticipates, identifies and resolves potential issues
- Completes all necessary and assigned training
Requirements
- Associates degree preferred or equivalent
- Experience in clinical research/pharma/biotech or related field considered
- Good knowledge of medical terminology, clinical data, and ICH/GCP preferred
- Ability to successfully prioritize and work on multiple tasks
- Strong attention to detail, accuracy and organizational skills
- Excellent communication, presentation, and interpersonal skills
- Ability to embrace new technologies
- health insurance
- retirement plans
- paid time off
- flexible work arrangements
- professional development
- total rewards program
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical researchmedical terminologyclinical dataICHGCP
Soft skills
attention to detailorganizational skillscommunication skillspresentation skillsinterpersonal skillsproblem-solvingprioritizationmultitasking
Certifications
Associates degree