Sr Clin Trials Asst (R1084956) in Amsterdam, NL at IQVIA™

Date Posted: 8/13/2019

Job Snapshot

  • Employee Type:
  • Location:
    Amsterdam, NL
  • Experience:
    Not Specified
  • Date Posted:
  • Job ID:

Job Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

Provide administrative support to clinical projects with minimal supervision from line manager, Clinical Team Leads and/or
other designated clinical team members. May assist with general administrative functions as required.
• Assist Clinical Team Lead (CTL) and Clinical Research Associates (CRAs) with accurately updating and maintaining
clinical systems that track site compliance and performance within project timelines.
• Collaborate with CTL on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports
according to the scope of work and standard operating procedures. Assist with periodic review of study files for accuracy
and completeness.
• Collaborate with CTL on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking
• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated
• Assist in training and orienting new staff. May act as a mentor for less experienced CTAs.
• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with
required approval.
• May perform assigned administrative tasks to support team members with clinical trial execution.
All responsibilities are essential job functions unless noted as nonessential (N).
• Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and
International Conference on Harmonisation (ICH) guidelines
• Knowledge of applicable protocol requirements as provided in company training
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
• Strong written and verbal communication skills including good command of English language
• Effective time management and organizational skills
• Attention to detail and accuracy in work
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
• School diploma/certificate or educational equivalent; or equivalent combination of education, training and experience
• Extensive use of telephone and face-to-face interactions, which require accurate perception of speech
• Extensive keyboarding involving repetitive motions with fingers
• Regular sitting for extended periods of time
• Packaging and lifting supplies for storage and shipping
• Occasional travel 

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job ID: R1084956