Site Research Assistant (Qcare) (Clinic-based in Champaign, IL) - (R1031027) in Champaign, IL at IQVIA™

Date Posted: 6/27/2018

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Champaign, IL
  • Experience:
    At least 2 year(s)
  • Date Posted:
    6/27/2018
  • Job ID:
    R1031027

Job Description

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Description

PURPOSE


Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to
collect data on patients enrolled and/or seeking enrollment in clinical studies.


RESPONSIBILITIES
  • Provide clinical research support to investigators and site staff, including:
    • Verify and/or correct research study information on source documents; research queries and variances; and provide feedback to the site data collector.
    • Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness.
    • Prepare and maintain research study files. Compile, collate and submit study information within established deadlines.
    • Collect and submit regulatory/ethics documentation pertaining to the research study.
    • Maintain the FDA 1572 form for assigned research studies.
    • Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.
    • Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.



All responsibilities are essential job functions unless noted as nonessential (N).

Job Requirements

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
  • Basic knowledge of clinical trials
  • In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
  • Basic knowledge of medical terminology
  • Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
  • Excellent interpersonal skills
  • Ability to pay close attention to detail
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE
  • High school diploma or educational equivalent and 2 years’ relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience
  • Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies

PHYSICAL REQUIREMENTS
  • Use of telephone and face-to-face communication requiring accurate perception of speech
  • Use of keyboard requiring repetitive motion of fingers
  • Frequent mobilization around the facility
  • Occasional lifting and moving objects weighing up to 10 lbs/4.5 kg


EEO Minorities/Females/Protected Veterans/Disabled

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.


Job ID: R1031027