Global Site Contracts Lead - Clinical Trials & Budgets

IQVIA; Bellville (TX); On-site; USD 90,000 - 130,000; Full time

Job summary

IQVIA is seeking an experienced professional to oversee clinical trial budgets and lead global negotiation activities. The role focuses on contract management, site sponsorship interactions, and timely delivery of compliant documents.

You will craft contracting strategies, coordinate investigator grants, and drive performance against financial and operational goals. This position requires strong negotiation, communication, and independent work skills in a regulated clinical trial environment.

Qualifications

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

Responsibilities

• Prepare, review, negotiate and manage clinical trial agreements with sites and sponsors.
• Serve as primary contact for investigative sites and sponsors.
• Tracks completion of all contractual documents for sites.
• Establish project timelines.
• Develop contracting strategies and coordinate investigator grants as applicable.
• Develop contract and budget templates, systems, tools, processes, and training materials.

Skills

Negotiation skills

Communication skills

Independent work capability

Drug development knowledge

Education

Bachelor's Degree in Scientific discipline or Healthcare

Job description

IQVIA is seeking an experienced professional to oversee clinical trial budgets and lead global negotiation activities. The role focuses on contract management, site sponsorship interactions, and timely delivery of compliant documents.

You will craft contracting strategies, coordinate investigator grants, and drive performance against financial and operational goals. This position requires strong negotiation, communication, and independent work skills in a regulated clinical trial environment.