Directly negotiate clinical study agreements and ancillary documents with investigative sites in support of global clinical trials with minimal oversight.
Help plan contract execution strategy for assigned studies.
ROLE RESPONSIBILITIES
Effectively negotiate legal terms and budgets with clinical trial sites in North America, to protect the Client’s interests while balancing the sites’ requirements
May review the rest of world’s budget escalations
Provides input into and supports global clinical site contracting and budgeting process and negotiation.
Collaborates and supports Client Study Teams
Apply and understand benchmark cost data, relationships, and trends to real-world situations.
Partner with Legal and other divisions to manage escalations in the site contracting space
Collaborates with invoicing specialists and/or invoice service providers to ensure alignment with Investigative
Site contracting and compensation requirements.
Applies acquired job skills and procedures to complete substantive assignments, projects, and tasks of moderate scope and complexity in applicable discipline.
BASIC QUALIFICATIONS
Bachelor’s degree is required with 5+ years of experience, or a Master’s degree with 3+ years of experience is required.
Experience with clinical trials, investigator budgets, and negotiation principles, practices, processes, and activities.
Balance of general business, compliance, finance, legal, and drug development experience is essential Strong and precise communications and presentation skills essential for success.
Demonstrated ability to lead by influence rather than positional power to accomplish critical deliverables.
PREFERRED QUALIFICATIONS
Advanced degree (JD, MBA or another graduate degree), professional qualification