Join a leading organization dedicated to enhancing patient outcomes through high-quality clinical studies. This role offers you the opportunity to work in a collaborative and dynamic environment focused on ensuring that site contracts are both cost-effective and aligned with industry standards.
As an ideal candidate, you are an accomplished
Site Contracts Manager
with a strong foundation in legal processes and excellent negotiation skills. If you excel in a fast-paced environment and have a keen eye for detail, this role could be the perfect fit for you.
* You lead negotiations of clinical study documents, including site agreements and budgets.
* You partner with study teams to identify protocol-specific and country-specific considerations for contracts.
* You customize contract templates in collaboration with Legal and IP departments.
* You develop realistic and study-appropriate budget ranges for investigator services.
* You prepare detailed project specifications and manage the site negotiation process.
* You ensure contracts accurately reflect the responsibilities of all parties involved.
* You track contract execution and ensure compliance with regulations and guidelines.
What are we looking for?
* You have at least
3 years of experience
in the pharmaceutical, biotechnology, or CRO industry.
* You possess strong negotiation and conflict-management abilities.
* You are an excellent communicator with strong verbal and written skills in English.
* You are proficient with
Microsoft Office
.
* You have strong organizational and time-management skills.
* You hold a
Bachelor's degree in science, finance, legal, or business
; a Master's degree is preferred.
* You demonstrate a proactive, adaptable, and results-driven mindset.
* You are capable of managing multiple priorities independently.
* You are proficient in
English
; additional languages are an advantage.