Join a transformative and collaborative environment where your expertise will play a crucial role in shaping high-quality, cost-effective contracts for clinical studies. Our client is looking for a professional who can drive excellence in study site contract management.
As the ideal candidate, you will be a proficient
Site Contracts Manager
with a strong legal or paralegal background. You thrive in fast-paced settings and demonstrate exceptional attention to detail, ensuring that all contracts align with industry standards.
* You lead negotiations of clinical study documents including site agreements, budgets, and informed consents.
* You partner with study teams to identify protocol-specific and country-specific considerations for contracts.
* You customize contract templates in collaboration with legal and related departments.
* You develop realistic budget ranges for investigator services.
* You manage contract negotiations, amendments, and scope changes effectively.
* You ensure compliance with applicable regulations and guidelines.
* You collaborate daily with colleagues and stakeholders to enhance contract management processes.
What are we looking for?
* You have a strong background with at least
3-5 years of experience
in the pharmaceutical, biotechnology, or CRO industry.
* You possess a
Bachelor's degree in science, finance, legal, or business
, with a Master's degree preferred.
* You have strong negotiation and conflict management capabilities.
* You exhibit excellent teamwork skills in a multicultural environment.
* You demonstrate a proactive, adaptable, and results-driven mindset.
* You have proficiency in
Microsoft Office
.
* You are fluent in
English
; additional languages are an advantage.