IQVIA
RWEAssociateSiteManagerwithGermanLanguage
“RWE Associate Site Manager with German Language at IQVIA. Skills: Site management, Study delivery, Remote monitoring, Data management. Ensure sites conduct study and report data. Perform initiation, remote monitoring, and close-out activities”
What You'll Achieve.
Ensure sites are conducting the study and reporting study data as required; Ensure timely mitigation of risks impacting delivery; Ensures timely transmission of clinical data; Works with sites to resolve data queries; Drive data cleaning and readiness for database lock; Site performance; Enrollment; Data quality; Delivery milestones
Industry & Context.
Good problem-solving skills; Apply critical thinking with guidance
GERMAN LANGUAGE IS MANDATORY, May monitor and/or co-monitor on-site when needed, Authorized to request onsite visits and/or audits, May provide guidance to less experienced clinical staff
What They're Looking For.
Must Have
Pre-intermediate knowledge of clinical research processes, Pre-intermediate knowledge of medical terminology, Pre-intermediate knowledge of ICH-GCP guidelines, Pre-intermediate knowledge of applicable regulations, Written and verbal communication skills, Good command of English language, Good organizational skills, Good problem-solving skills, Ability to manage multiple priorities, Ability to meet deadlines, Ability to adhere to project timelines, Ability to work independently on routine tasks, Ability to apply critical thinking with guidance, Ability to build and maintain effective relationships with sites, colleagues, and stakeholders, Computer skills including Microsoft Word and Excel, GERMAN LANGUAGE IS MANDATORY
Nice to Have
Bachelor's Degree (scientific discipline or health care preferred), Minimum of 1 year of relevant clinical experience, Equivalent combination of education, training and experience may be acceptable, Working knowledge of study execution and delivery lifecycle, Understanding of electronic data capture (EDC) systems, Understanding of data review processes, Understanding of different study designs, Understanding of their operational implications
What You'll Do.
Ensure sites conduct study and report data
and close-out activities
Serve as primary contact between business and investigator site
Perform site management and delivery activities
and document site issues
Review quality and integrity of patient data
Drive data cleaning and readiness for database lock
Ensure accurate completion and maintenance of internal systems
Provide input and updates regarding site performance
Escalate risks or delays as needed
How You'll Work.
Team & Collaboration
Works collaboratively with other functional groups; Collaborate with assigned field CRAs; Build and maintain effective relationships with sites, colleagues, and stakeholders
Communication Scope
Written communication skills; Verbal communication skills; Good command of English language
Process & Methodology
Manage multiple priorities across different sites and studies, Adhere to project timelines
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