Clinical Research Associate 2, Sponsor Dedicated, Johannesburg based

Posted 2 Days Ago
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Centurion, City of Tshwane Metropolitan Municipality, Gauteng, ZAF
In-Office
Junior
Healthtech
The Role
The Clinical Research Associate II performs monitoring and management for clinical studies, ensuring compliance with protocols and regulations, supporting site recruitment and assessment, and collaborating with study teams.
Summary Generated by Built In
Clinical Research Associate II (CRA II)

Sponsor Dedicated

Johannesburg Based

Job Overview

The CRA II performs site monitoring and management activities to ensure clinical studies are conducted in accordance with study protocols, applicable regulations, and sponsor requirements.

Key Responsibilities

  • Conduct site monitoring visits (selection, initiation, routine monitoring, and close-out) in line with GCP, ICH guidelines, and contracted scope

  • Drive and support subject recruitment strategies at site level to meet enrollment targets

  • Deliver protocol and study-related training and maintain effective communication with investigative sites

  • Assess site performance to ensure quality, data integrity, and regulatory compliance; escalate issues as needed

  • Track study progress including regulatory submissions, enrollment, CRF completion, and query resolution; support study start-up where required

  • Ensure essential documents are complete and filed appropriately in the TMF and maintained in the Investigator Site File (ISF)

  • Prepare monitoring reports, follow-up letters, and maintain accurate site documentation

  • Collaborate with cross-functional study teams to support project delivery

  • Support site-level recruitment planning and, where applicable, site financial management activities

Qualifications & Experience

  • Bachelor’s degree in life sciences or healthcare (or equivalent combination of education and experience)

  • Minimum 2 years of on-site monitoring experience

  • Mandatory Oncology therapeutic area experience

  • Strong knowledge of GCP, ICH guidelines, and clinical research regulations

  • Good therapeutic area and protocol understanding

  • Proficiency in Microsoft Office (Word, Excel, PowerPoint)

  • Strong communication, organizational, and problem-solving skills

  • Ability to manage time, priorities, and stakeholder relationships effectively

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 https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Skills Required

  • Bachelor's degree in life sciences or healthcare
  • Minimum 2 years of on-site monitoring experience
  • Mandatory Oncology therapeutic area experience
  • Strong knowledge of GCP, ICH guidelines, and clinical research regulations
  • Proficiency in Microsoft Office

IQVIA Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about IQVIA and has not been reviewed or approved by IQVIA.

  • Healthcare Strength Healthcare coverage is positioned as comprehensive, spanning medical/dental/vision plus programs like telemedicine, EAP resources, and additional insurance options. Feedback suggests the health offering is a meaningful part of the overall rewards package, though details can vary by location and plan design.
  • Retirement Support Retirement benefits include an employer match structure that supports employee contributions through a defined formula. This adds steady long-term value to total rewards beyond base salary.
  • Leave & Time Off Breadth Time off offerings include vacation/paid time off, holidays, and flexibility themes, with some roles described as having discretionary or unlimited time-off models. This can make the package feel more attractive even when cash compensation is viewed as only mid-range.

IQVIA Insights

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The Company
Bangalore, Karnataka
61,500 Employees
Year Founded: 2016

What We Do

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.

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