Site Management Coordinator

By its name, IQVIA Company is prominently recognized as a multinational company serving the combined industries of health information technology and clinical research.

A Site Management Coordinator creates all digital campaign strategy, buying, reporting, analysis, optimization, and boosts client engagement.

To understand more perspectives concerning Site Management Coordinator, including the requirements and duties, you must digest the following information below.

Job Details

• Job Category: Managing Editor
• Name of company: IQVIA Company
• Location: Frankfurt, Germany
• Salary: €77861 per year
• Schedule: Full-Time.

Company Description

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.

Under general supervision, perform tasks at a country level associated with site activation activities by applicable local and international.

They believe in pushing the boundaries of human and data science to make the most significant impact possible – to help our customers create a healthier world.

Regulations, standard operating procedures (SOPs), project requirements, and contractual/budgetary guidelines; may also include maintenance activities.

Essential Functions

• Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs, and work instructions.
• Site Activation Manager (SAM), Project Management team, and other departments as necessary.
• Review documents for completeness, consistency, and accuracy under the guidance of senior staff.
• Prepare site regulatory documents, reviewing for completeness and accuracy.
• Inform team members of completing regulatory and contractual documents for individual sites.
• Distribute completed documents to sites and internal project team members.
• Support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information.
• Review, track and follow up on the progress, approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release papers.

Qualifications

• Three years of experience in an administrative environment or equivalent combination of education, training, and experience.
• German language skills are a Must.

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