Your role:
As the Head of Clinical Agreements, you will lead the team responsible for managing Site and Health Care Professional (HCP) Agreements for Clinical Trials. You will provide strategic direction, coaching, and technical support to foster a collaborative team environment. Your expertise will be crucial in developing negotiation strategies, ensuring compliance with regulatory standards, and driving process improvements to enhance operational efficiency.
As the subject matter expert, you will oversee complex negotiations, including budget discussions, ensuring timely and effective resolutions. You will be accountable for the execution, performance, and quality metrics of Clinical Agreements at the portfolio level, identifying trends and gaps that may affect key deliverables.
Additionally, you will coordinate revisions of Master Clinical Site Agreement templates, Legal Manuals, and negotiation guidance documents in collaboration with both internal and external partners. This position presents an exciting opportunity to contribute to the advancement of clinical research and improve lives through innovative solutions.
Who you are:
You have a minimum of 10 years of experience in clinical research, focusing on clinical trial contract and budget negotiation/management.
You hold a Master’s degree in a related field, preferably in law or paralegal studies.
You possess in-depth knowledge of clinical trial regulations, contract law, and industry standards (FDA, ICH-GCP, etc.).
You demonstrate strong leadership skills and the ability to drive process improvements.
You have excellent negotiation and communication skills, enabling you to manage complex discussions effectively.
You are skilled in developing and maintaining strong working relationships with internal and external stakeholders.
You are proactive in identifying risks and inefficiencies, with a focus on operational excellence.
You are committed to fostering a culture of inclusion and belonging within your tea...