Site Research Assistant Kansas City, MO

IQVIA

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profile Job Location:

Parsippany, NJ - USA

profile Hourly Salary: $ 25 - 39
Posted on: 4 hours ago
Vacancies: 1 Vacancy

Job Summary

Job Title: Research Assistant

Work Set-Up: On-site
Scheduled Weekly Hours: 20 Hours

Job Profile Summary:

We are seeking a detail-oriented Research Assistant to support clinical trial activities in compliance with all applicable regulations. This role requires strong organizational skills logical thinking adaptability and excellent interpersonal and team-building abilities.

Key Responsibilities:

  • EDC entry and query resolution
  • Maintain regulatory binder and ensure compliance with documentation standards
  • Schedule and coordinate subject visits and procedures
  • Develop strong working relationships and maintain effective communication with study team members
  • Build trust and respect with investigators and office staff
  • Assist with screening recruiting and enrolling research subjects
  • Perform patient/research participant scheduling and collect history
  • Coordinate follow-up care and laboratory procedures
  • Adhere to IRB-approved protocols and assist in informed consent processes
  • Support the safety of research subjects
  • Comply with company and Sponsor policies SOPs and guidelines

Qualifications:

  • Minimum of an associates degree or equivalent education and experience
  • At least 1 year of experience in a clinical research setting preferred
  • Working knowledge of clinical trials and Good Clinical Practices (GCP)
  • Familiarity with protocol-specific procedures consent forms and study schedules
  • Proficiency in EDC entry and query resolution
  • Experience in visit scheduling and regulatory binder upkeep
  • Strong attention to detail and ability to prioritize tasks
  • Excellent communication and relationship-building skills
  • Applicable certifications and licenses as required by company state or regulatory bodies

Please note: This position is not eligible for sponsorship.

#LI-CES #LI-DNP #LI-HCP #ONSITE

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and/or schedule (full or part-time). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and welfare and/or other benefits.


Required Experience:

Junior IC

Job Title: Research AssistantWork Set-Up: On-siteScheduled Weekly Hours: 20 HoursJob Profile Summary:We are seeking a detail-oriented Research Assistant to support clinical trial activities in compliance with all applicable regulations. This role requires strong organizational skills logical thinkin...
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Key Skills

  • Laboratory Experience
  • Spss
  • Data Collection
  • DNA Isolation
  • Stata
  • Biochemistry
  • Qualitative Research Interviewing
  • Research Experience
  • Statistical Software
  • Molecular Biology
  • Research Laboratory Experience
  • Western Blot

About Company

Company Logo

IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more

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