Study Contract Manager, Europe

Rho Inc is seeking a Study Contract Manager, Europe to join our growing team dedicated to excellence in clinical research contract management. In this senior role, you will lead contract negotiations and management activities for clinical study agreements in the European Union, ensuring compliance with regional regulations and alignment with our company’s strategic goals. As a Study Contract Manager, you will collaborate closely with cross-functional teams including legal, business development, finance, and study operations to develop, negotiate, and finalize contracts that protect company interests and facilitate successful study execution. You will serve as a key point of contact for clients and vendors, demonstrating expertise in clinical research contracting across the European market. We offer a dynamic environment that promotes professional development and values your expertise in contract management within the clinical research industry. Responsibilities Lead negotiation, drafting, and execution of clinical study contracts, budgets and related agreements within the EU region. Collaborate with internal stakeholders such as legal, finance, business development, and study teams to ensure contract terms meet company objectives and compliance requirements. Manage contract workflows to meet study timelines and client expectations. Provide strategic guidance on contractual risks and opportunities related to regional compliance and regulatory environments. Maintain strong relationships with clients and vendors, serving as a trusted advisor on contract matters. Support process improvements and standardization initiatives within the contract management function. Keep up to date with industry trends, regulations, and best practices in clinical study contracting in the EU. Bachelor’s degree in Business, Law, Life Sciences, or related field; advanced degree or certifications in contract management preferred. Minimum of 5 years of experience in clinical research contract management, with strong focus on EU-based study agreements. Budget negotiation experience is preferred. In-depth knowledge of clinical trial regulations, local laws, and compliance requirements within the EU. Proven ability to negotiate complex contracts and manage multiple stakeholders effectively. Excellent communication and interpersonal skills, capable of interacting with diverse internal and external teams. Strong organizational skills and attention to detail, with ability to manage competing priorities in a fast-paced environment. Proficiency with contract management systems and Microsoft Office suite. Fluency in English required; additional European languages considered a strong asset. Flexibility: We encourage a work-life balance that allows employees to bring their best selves to work while being passionate about their lives outside work.