Parexel Work Values

Daily Duties at Parexel:

• Responsible for site management including tracking regulatory submissions and approvals, recruitment and enrollment, data query resolution, and supply management. • Served as Co-Clinical Lead performing such duties as addressed protocol questions,team communication point of contact, and provide site and CRAs issue escalation • Conducted qualification, initiation, monitoring, and termination study visits. • Reviewed informed consent documents and study protocols to ensure accuracy, compliance, and proper implementation. • Prioritize multiple tasks/projects and provided direction and team leadership on projects. • Assisted with quality assurance audits and resolution of Sponsor audits. • Provided monitoring assessments for entry level CRAs and served as a mentor. • Conducted protocol and specific study training to clinical investigators and site personnel

What they like about Parexel:

You highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

Tags

Sr. Clinical Research Associate , Project Manager , Clinical Trial Manager

Skills

Presentation, Ecommerce Strategy and digital marketing channels optimization - SEO, SEM, email, affiliates - for high-profile accounts., Technology Solutions, Sales Support, Leadership

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