Clinical Research Associate - Negotiations and Compliance

GForce Life Sciences is a leading company in the medical device industry, and we are currently seeking a skilled Clinical Research Associate - Negotiations and Compliance to join our team.
About the Role

This role offers a unique opportunity to work in a dynamic environment, where you will be responsible for negotiating, reviewing, and processing clinical study and research contracts and budgets. As a key member of our team, you will be working under the direction of a manager or senior contract associate, providing technical assistance, and ensuring quality work.

Key Responsibilities:
• Sending initial contract/budget email to invited sites within specified timelines
• Scanning of fully executed contracts and revised Investigator agreements
• Uploading of documents to electronic trial master file system and maintaining status notes
• Supporting Contracts Manager & Associates as required on assigned tasks

Requirements:
• Minimum of 1-3 years related work experience in clinical research
• Associate's or Bachelor's Degree in Business Administration, a related field, or equivalent
• Negotiations/Skills in redlining documents and analytical experience or equivalent
• Familiarity with grant and contract requirements, policies, and procedures including, but not limited to:
• Knowledge and understanding of GCP, ICH, GLP and other federal, state, industry rules and regulations governing technical aspects of clinical grants and contracts
• Ensure all required data from studies and sites to comply with regulatory and government requirements (Sunshine Act, FWA, Human Subject Protection training, Clinical Insurance)

What We Offer:
• Contract through the EOY with potential to extend
• Benefits available (Medical, Dental, Vision, 401k)