Clinical Trials Assistant (R1122483) in Seoul,SK at IQVIA™

Date Posted: 3/10/2020

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Seoul,SK
  • Experience:
    Not Specified
  • Date Posted:
    3/10/2020
  • Job ID:
    R1122483

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.

PURPOSE

Provide administrative support to clinical projects under direction of line manager, Clinical Team Leads and/or other

designated clinical team members. May assist with general administrative functions as required.

RESPONSIBILITIES

  • • 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.

  • • Assist the clinical team in 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.

  • • Assist CTLs with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • • 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

documentation.

  • • May perform assigned administrative tasks to support team members with clinical trial execution.
  • • All responsibilities are essential job functions unless noted as nonessential.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  • • Awareness of 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

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

  • • School diploma/certificate or educational equivalent; or equivalent combination of education, training and experience

PHYSICAL REQUIREMENTS

  • • 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: R1122483