Clinical Trial Contracts Specialist

Iqvia; England; Sur place; GBP 40 000 - 56 000; Plein temps

Résumé du poste

IQVIA is seeking a Contract Negotiator within Clinical FSP to accelerate study start-up by negotiating site agreements and ensuring regulatory compliance. You will partner with sponsors, investigative sites, legal teams and cross-functional stakeholders to deliver contracts on time and within budget.

In this role you will leverage your negotiation expertise to resolve issues, mitigate risks and support study start-up timelines.

Qualifications

• Bachelor's degree or equivalent.
• 3-5 years of experience in clinical research contract management or a similar role.
• Familiarity with clinical trial processes regulatory requirements and contract lifecycle management.
• Strong analytical organizational and communication skills.

Responsabilités

• Negotiate clinical trial contracts with research sites, ensuring agreements are completed on time and meet quality and compliance requirements.
• Manage contract changes and additional agreements while balancing business needs and regulatory requirements.
• Support contract planning and study start-up activities for assigned sponsors, studies, and programs.
• Help develop investigator grants, site budgets, contracting plans, and proposal documents.
• Prepare and negotiate contract terms, payment schedules, and budget templates based on project and sponsor needs.
• Work closely with sponsors, stakeholders, and regional study start-up teams to achieve project goals and timelines.
• Provide contract-related guidance and support to study teams on operational and financial matters.
• Gather and share contract and market information to support study planning and decision-making.
• Monitor contract activities to ensure timelines, milestones, and financial goals are met.

Connaissances

Analytical skills

Organizational skills

Communication skills

Formation

Bachelor's degree or equivalent

Description du poste

IQVIA is seeking a Contract Negotiator within Clinical FSP to accelerate study start-up by negotiating site agreements and ensuring regulatory compliance. You will partner with sponsors, investigative sites, legal teams and cross-functional stakeholders to deliver contracts on time and within budget.

In this role you will leverage your negotiation expertise to resolve issues, mitigate risks and support study start-up timelines.