📌 OPPORTUNITY OVERVIEW

IQVIA is actively recruiting for a Clinical Trial Manager - IQVIA Biotech - Centurion position in Gauteng. This is an excellent opportunity for professionals in the Medical / Healthcare sector looking to advance their careers.


🎯 IDEAL CANDIDATE PROFILE
We are seeking talented individuals with the following profile

• Experience Level: 5 years • Educational Background: Bachelor or equivalent • Industry Focus: Medical / Healthcare • Location Preference: in Gauteng


💼 WHY THIS ROLE MATTERS

Healthcare professionals including Clinical Trial Manager - IQVIA Biotech - Centurion are essential service providers. This role contributes directly to community health and wellbeing.


📈 CAREER DEVELOPMENT INSIGHTS

This role in Medical / Healthcare offers valuable career progression opportunities aligned with your experience level and professional aspirations.


📋 APPLICATION GUIDANCE

When applying for this Clinical Trial Manager - IQVIA Biotech - Centurion position, ensure your CV highlights: • Relevant experience matching the 5 years requirement • Educational qualifications in line with Bachelor • Specific achievements in the Medical / Healthcare field • Any certifications or specialized training


🌍 SOUTH AFRICA JOB MARKET CONTEXT

The Medical / Healthcare sector in South Africa continues to show strong demand for skilled professionals. This position represents a valuable opportunity in the current job market.

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Job Overview

Clinical Trial Managers (CTM) are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. The CTM is a member of the core project team responsible for clinical delivery of full service, large, multi-regional studies to meet contractual requirements and in accordance with (Standard Operating Procedures) SOPs, policies and practices.

Essential Functions

Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans). Accountable for meeting projects’ recruitment targets and ensuring appropriate recruitment strategies are in place. Contribute to the development of the project risk mitigation plan. Manage clinical risks through the project lifecycle. Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues. Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work. Work as the primary CTM alongside other CTMs to deliver large, global trials. Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management. Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements. Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings. Conduct regular team meetings and communicate appropriately to achieve objectives. Support professional development by providing feedback to clinical team line managers on performance relative to project tasks to support professional development. Adopt corporate initiatives and changes and serve as a change advocate when necessary. May contribute to the development of the clinical delivery strategy for business proposals. Participate in bid defense preparations and meetings. Develop and present Clinical Operation plan in partnership with Business Development and Project Leadership. May mentor and coach new peers as they assimilate into this role. May attend site visits as applicable in support of project delivery.


Qualifications

Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required


Experience

Ideally at least 5 years experience in clinical trial management or equivalent combination of education, training and experience. Requires consolidated knowledge of Project management practices and terminology. Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Requires broad protocol knowledge and therapeutic knowledge.; Req Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates. Requires understanding of project finances. Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;

How To Apply
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  • Attach your Application letter, updated Curriculum Vitae (CV) and any supporting documents required.
  • Use a professional subject line such as Application for "Indicate Positions"
  • Send your application before the closing date.

Note: Only shortlisted candidates are contacted.

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Salary

0 - 0 ZAR

Monthly based

Location

Gauteng

Job Overview
Job Posted:
3 weeks ago
Job Expire:
1 month from now
Job Type
Contract
Job Role
Entry level role
Education
Bachelors/Higher National Certificate
Total Vacancies
Variable
Category
Medical / Healthcare

Share This Job:

Location

Gauteng

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