Clinical Contracts Associate

Clinical Contracts Associate at GForce Life Sciences Clinical Contracts Associate at GForce Life Sciences in Hamel, Minnesota Posted in 1 day ago.

Type:

full-time

Job Description:

Clinical Contracts Associate 6-month + Onsite in Maple Grove, MN Responsibilities Creating and negotiating Amendments Preparing study-site specific budget drafts Sending initial contract/budget email to invited sites within specified timelines Periodic follow up with sites Submitting finalized contracts for signatures Scanning of fully executed contracts and revised Investigator agreements Uploading of documents to electronic trial master file system and maintaining status notes Attending calls and providing regular status updates as required Filing of hard copy contracts Preparing NTA agreement templates and sending out to sites Licensing requests Supporting Contracts Manager & Associates as required on assigned tasks Qualifications 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. Required Skills Negotiations/Skills in redlining documents and analytical experience or equivalent. Familiarity with grant and contract requirements, policies, and procedures including, but not limited to: Clinical and AdvaMed Code of Ethics on Interactions with Health Care Professionals. 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).