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Centralized Monitor, Office Based South Africa

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IQVIA

16d ago

  • Job
    Full-time
    Junior Level
  • Research & Development
    Healthcare
  • Pretoria
    Remote

AI generated summary

  • You need a Bachelor's in life sciences, at least 1 year in clinical research, strong problem-solving skills, attention to detail, tech-savvy, and effective communication across cultures.
  • You will monitor study quality, maintain databases, manage triggers, analyze data trends, participate in meetings, escalate issues, review data accuracy, and interact with sites throughout the project lifecycle.

Requirements

  • Someone who understands dynamics of working with the sites?
  • Results driven and detail-oriented?
  • Good at supporting others on problem solving?
  • Good at planning, time management and prioritization?
  • Skilled at software and computer use, that enjoys technology applied to data analysis?
  • Understands clinical trial conduct, and skill in applying applicable clinical research regulatory requirements and relevant local laws, regulations and guidelines?
  • Able to communicate efficiently and work well across cultures and geographies?
  • You must have a Bachelor's degree in life sciences or related field
  • At least 1 year experience in clinical research field preferred.

Responsibilities

  • Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs respective regulations and guidelines.
  • Ensure accurate completion and maintenance of internal systems, databases, tracking tools/reports for the project specific information.
  • May perform Management of triggers and preparation of i-site pack for respective sites and countries for assigned study(ies).
  • May assist in Developing required basic data analytics scope and performing the trend analytics for their respective study(ies).
  • May participate in (study) team meetings and interaction with cross functional staff to verify information and/or triage new data issues or prior identified action items.
  • Escalate quality issues pertaining to site to respective Centralized Monitoring Lead / Sr. Centralized Monitor.
  • May perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy.
  • Review any other information as necessary to determine overall readiness of the patient information for next level review.
  • Interaction with sites/CRA and follow-up on study required milestones from the project start until close out.

FAQs

What is the role of a Centralized Monitor?

A Centralized Monitor (CM) is a skilled and clinically experienced team member who provides remote project support and assistance across multiple projects, sites, and teams, reviewing structured clinical data while accessing medical charts.

What qualifications are needed to apply for the Centralized Monitor position?

You must have a Bachelor's degree in life sciences or a related field, along with at least 1 year of experience in the clinical research field preferred.

What skills are important for a Centralized Monitor?

Important skills include understanding site dynamics, being results-driven and detail-oriented, supporting problem-solving, effective planning and time management, proficiency with software and technology for data analysis, knowledge of clinical trial conduct and regulations, and strong communication skills across cultures.

What are the key responsibilities of a Centralized Monitor?

Responsibilities include performing centralized monitoring activities, ensuring accurate completion of internal systems, management of triggers, assisting in data analytics, participating in study team meetings, escalating quality issues, performing subject-level data reviews, and interacting with sites/CRA to follow up on study milestones.

Is experience necessary for this position?

Yes, at least 1 year of experience in the clinical research field is preferred for this position.

Does the role of Centralized Monitor require onsite visits to clinical sites?

No, the Centralized Monitor provides remote monitoring and support without requiring onsite visits.

What type of projects will the Centralized Monitor work on?

The Centralized Monitor will work on multiple projects across various sites, ensuring the quality and integrity of studies as per the protocol and respective regulations.

Can I apply for this position if I do not have clinical research experience?

It is preferred to have at least 1 year of experience in the clinical research field; however, if you possess a relevant background and demonstrate the necessary skills, you may still consider applying.

Where can I learn more about IQVIA and their job offerings?

You can learn more about IQVIA and their job offerings by visiting their official careers page at https://jobs.iqvia.com.

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IQVIA

Accelerate innovation for a healthier world.

Science & Healthcare
Industry
10,001+
Employees

Mission & Purpose

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 86,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures.

Benefits

  • Medical, dental and vision coverage

  • Employee Assistance Programs

  • Mental health support

  • Flexible work environment

  • Time off for leisure, personal time and corporate holidays

  • Parental leave for birth or adoption

  • Paid leave for other life matters (i.e., illness, bereavement, jury duty, military service, etc.)

  • Retirement and savings plans

  • Commuter benefits

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