As a Senior Contract Analyst, you will manage agreements, ensure compliance, and support project teams in contract interpretation and execution.

Act as strategic liaison to investigator sites, build long-term relationships, support multiple studies, escalate operational issues, align site capabilities with study opportunities, monitor performance metrics, and drive site engagement and improvement initiatives.

Support review, drafting and negotiation of site contracts and budgets for clinical trials; track status and timelines, liaise with stakeholders, ensure accurate documentation, and contribute to process improvements under senior guidance.

Lead monitoring activities for APAC studies, ensure compliance, provide oversight, deliver training, and support project communications and issue resolution.

As a Clinical Research Associate, you'll conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with investigators.