Site Contract Specialist – Clinical Trials

About the role

Join a global team supporting leading pharmaceutical companies and biotech firms by managing site contracts for clinical trials. You will draft, negotiate, and finalize agreements while ensuring compliance and risk mitigation.

Key responsibilities

• Draft, review, negotiate and finalize agreements with study sites according to established processes.
• Coordinate with internal functional departments to align site startup activities with contractual timelines and achieve target activation cycle times.
• Identify, assess and escalate legal, financial and operational risks, providing recommendations for resolution.
• Ensure compliance with budgetary guidance, templates, authority approvals and client expectations.

Required profile

• Bachelor’s degree or equivalent with 2‑5 years of relevant experience.
• Good understanding of contract law principles, including business, IP and local tax regulations.
• Strong analytical, decision‑making and attention‑to‑detail skills.
• Ability to work independently or within a team and manage competing priorities.

Required skills

• Knowledge of contract negotiation and investigator grant budgeting.
• Familiarity with pharmaceutical product development processes and CRO involvement.
• Effective written and verbal communication in English.