Bridge Project: Assistant Resident Engineer

Surbana Consultants Pte Ltd – Kingdom Of Saudi Arabia; Cape Town; On-site; ZAR 750,000 - 1,250,000; Full time

Job summary

IQVIA in South Africa seeks a Global Site Contracts Manager to oversee contract negotiations for clinical trials across sites in South Africa and globally. You will manage budgets, timelines, and key stakeholder relationships to ensure compliant, timely agreements.

The role requires a science or healthcare background, 3–5 years experience, and strong negotiation and communication skills to coordinate with sponsors, investigators, and internal teams.

Qualifications

• Minimum 3–5 years of relevant contracts experience.
• Bachelor's Degree in a scientific discipline or healthcare.
• Strong negotiation and communication abilities.

Responsibilities

• Prepare, review, negotiate and manage clinical trial agreements with sites and sponsors.
• Serve as primary contact for investigative sites and sponsors.
• Ensure tracking of all contractual documents and establish project timelines.
• Develop contracting strategies and templates to support proposal development.
• Coordinate budgets and grant activities as applicable and proposal text.
• Develop contracting systems, tools, processes, and training materials.

Skills

Negotiation

Communication

Independent work

Education

Bachelor's Degree in Science/Healthcare

Job description

Global Site Contracts Manager - South Africa

Centurion, South Africa
Bloemfontein, South Africa
Bellville, South Africa
Full time
R

Responsible for overseeing clinical trial budgets and leading negotiation activities on a global scale

Essential Functions

• Preparation, review, negotiation and management of clinical trial agreements with sites and sponsors
• Serves as the primary point of contact for investigative sites and/or sponsors;
• Ensures tracking completion of all contractual documents for sites
• Establishes project timelines.
• Establishes and/or executes goals and objectives for team(s) as well as tracking and delivering on operational/financial performance.
• Responsible for the development of complex contracting strategies, coordination of investigator grants, as applicable and proposal text to support the proposal development process.
• Develop contract and budget templates and contracting systems, tools, processes, and training materials

Qualifications

• Bachelor's Degree in Scientific discipline or Healthcare
• 3 to 5 years prior relevant experience
• Good negotiating and communication skills with ability to challenge.
• Thorough understanding of regulated clinical trial environment and knowledge of drug development process
• Goal oriented, self-starter with proven ability to work independently.

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 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.
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