Contract Administrator III

This is not a temp to hire position.
Possible extension-

This legal department position will support clinical studies across a global organization through preparation, review and negotiation of a high volume of clinical study agreements and related agreements/documents by working with global internal business partners and external vendors to facilitate the contracting process.

• Using Client approved templates, prepare global clinical study agreements and related agreements and documents (e.g., informed consent forms, hospital use agreements, device purchase agreements) for ***-sponsored studies performed at clinical sites located around the globe.
• Independently review revisions proposed by clinical sites and revise based upon client's practices and procedures.
• Raise contract issues as appropriate and liaise between Legal, Risk Management, clinical teams and other internal stakeholders to resolve such issues.
• Ability to manage and prioritize a high-volume workload in a fast-paced working environment.
• Interface with *** Clinical, Contract Research Organizations and Global Clinical Operations contract support teams.
• Ensure agreements and other related documents are executed properly and uploaded to the contract management system.
• Organize and maintain contract management system and Microsoft Teams folders.

• 5+ years of professional experience with bachelors degree; OR High School Diploma or GED or associate degree with 7+ years in a related role, preferably within the legal department of a medical device or pharmaceutical company.
• Thorough understanding of clinical contracting terms and conditions.
• Global Clinical contracting experience required (non-negotiable).
• Able to read and understand contract terms, redline agreements, and make decisions with a practical, business-minded approach to contract negotiation.
• Strong computer skills (including Microsoft Office and Adobe software) with advanced skills with Word, Excel, and PowerPoint.
• Good communication skills.

• Med device experience a plus.
• Capable of coordinating and prioritizing multiple tasks/projects while maintaining accuracy and meeting deadlines.
• Capacity to interact professionally with internal stakeholders across the globe.