Experienced Clinical Research Associate - Multi Sponsored
Core
Perform site monitoring and management to ensure clinical studies are conducted per protocol and regulations, managing data integrity and site operations.
Role type
Clinical Research Associate (monitoring)
Builds
Clinical trial data and site compliance
Domain
Life sciences / Clinical research
Required skills
GCP and ICH guidelines knowledge, site monitoring execution, subject recruitment management, protocol administration, regulatory submission tracking, TMF/ISF management, documentation generation, financial management, therapeutic knowledge
Preferred skills
Bachelor's degree in scientific discipline or healthcare, on-site monitoring experience, computer proficiency (Word, Excel, PowerPoint, mobile devices), Arabic fluency, English command (via careerplan.io/jobs/R1564999-experienced-clinical-research-associate-multi-sponsored-at-iqvia)
Technologies
Microsoft Word, Excel, PowerPoint, laptop, iPhone, iPad
Responsibilities
Conduct site monitoring visits (selection, initiation, monitoring, close-out), drive subject recruitment plans, administer protocol training, evaluate site quality and adherence, track regulatory submissions and data completion, maintain Trial Master File and Investigator's Site File, generate visit reports and action plans, manage site financials and invoices
Seniority
Entry-level to Mid-level, hands-on IC