Parexel Int Work Values

Daily Duties at Parexel Int:

Responsibilities included the coordination and conduct of in-house monitoring activities, review and tracking of site regulatory packages, database set-up and maintenance for several studies concurrently. Collect and maintain trial master file documents, Screening logs, EDC set-up, record meeting minutes at team meetings, mentor new hire clinical research assistants and support the clinical team to ensure that the investigators and site staff followed Good Clinical Practices, ICH and FDA Regulations.

What they like about Parexel Int:

You give high priority to hiring firms with prestige. Market reputation and prestige of a firm may be determined through on-line research, and conversations with individuals working in your target industry. Note that firms "in the public eye" receive a great deal more critical publicity and attention than those operating with more anonymity. So as you assess your employment opportunities, be sure to seek out the positive aspects of the firm's reputation in addition to noting negative publicity the company may have received.

Tags

clinical research, medical affairs, Clinical research Associate, Clinical Research Assistant, Clinical Development Associate, Clinical Development Assistant, Regulatory Affairs Associate, Regulatory Affairs Assistant, Drug Safety Associate, Drug Safety Assistant, Clinical Development, Clinical Trials Associate, Clinical Trials Assistant

Skills

P&L responsibilities, Presentation, Ecommerce Strategy and digital marketing channels optimization - SEO, SEM, email, affiliates - for high-profile accounts., Technology Solutions, Sales Support, Software Implementation, Requirements Analysis & Specification, Leadership

These are some of the questions we asked our climbers about their experiences with Parexel Int: