Site Contract Specialist II

Triwill Group; India; On-site; INR 1,000,000 - 1,800,000; Full time

Job summary

Triwill Group, acting for a partner company, seeks a Site Contract Specialist II based in India. The role supports management and execution of clinical trial site contracts across multi-country studies, coordinating contracts, budgets, amendments, documentation, and approvals to meet timelines and quality standards.

Working closely with clinical operations, legal, finance, vendors, investigators, and sponsors, you will help resolve contractual and budgetary issues efficiently and contribute to

Qualifications

• Experience in contract negotiation and review within clinical or regulated environments.
• Ability to manage budgets, amendments, and contract documentation.
• Strong written and verbal communication with cross-functional teams.

Responsibilities

• Coordinate site contracts, budgets, amendments, documentation, and approvals.
• Support timelines and quality standards across studies.
• Collaborate with clinical operations, legal, finance, vendors, investigators, and sponsors to resolve issues.
• Engage in contract management, negotiation, project coordination, and stakeholder communications.
• Contribute to process improvements, QA, training, and mentorship for junior staff.

Skills

Contract negotiations

Budget management

Documentation

Stakeholder communication

Attention to detail

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Site Contract Specialist II based in India.

This role supports the successful management and execution of clinical trial site contracts across complex, often multi-country studies.
You will coordinate contracts, budgets, amendments, documentation, and approvals while ensuring timelines and quality standards are consistently met.
Working closely with clinical operations, legal, finance, vendors, investigators, and sponsors, you will help resolve contractual and budgetary issues efficiently.
The position combines contract management, negotiation, project coordination, and stakeholder communication in a fast-paced clinical research environment.
You will also contribute to process improvements, quality assurance, training, and the development of less experienced team members.
Strong attention to detail and an understanding of clinical development and contracting requirements will be essential to keeping studies moving forward.
This is an opportunity to contribute to global clinical programs that help bring important therapies to patients more efficiently.