Senior Site Contracts Specialist

Key Responsibilities:

• Draft, negotiate, finalize, and execute clinical site agreements, ancillary agreements, and amendments at the country or regional level.
• Track progress of site contracting activities during study startup or maintenance and provide contingency plans for delays.
• Collaborate with Site Contracts Lead, project management, clinical management, and clinical operations to meet project goals.

Qualifications:

• Undergraduate or graduate degree in business, law, or life sciences; or equivalent combination of education and experience.
• Extensive experience (preferably 4+ years) negotiating CSAs and Investigator grants; strong knowledge of applicable regulations and country-specific requirements.
• Excellent attention to detail, communication skills, and ability to manage multiple tasks with sound independent judgment.

Additional Information:

• Work remotely from select US states (Florida, Georgia, South Carolina, etc.) with a team that values quality, integrity, and agility.
• Join a global organization where culture matters as much as capability, with real commitment to work-life balance and career growth.