
10,000+ employees
Founded 2010
đ§Ź Biotechnology
đĽ Healthcare
đ Pharmaceuticals
Biotechnology ⢠Healthcare ⢠Pharmaceuticals
BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.
đĽ 8 minutes ago
đŞđ¸ Spain â Remote
đľ âŹ57.6k - âŹ72k / year
â° Full Time
đ Senior
⨠Associate
đť Ghost score 1%
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10,000+ employees
Founded 2010
đ§Ź Biotechnology
đĽ Healthcare
đ Pharmaceuticals
Biotechnology ⢠Healthcare ⢠Pharmaceuticals
BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.
⢠Draft, negotiate, and finalize complex clinical site contracts throughout the clinical trial lifecycle ⢠Prepare, negotiate, and finalize clinical trial agreements, ancillary agreements, amendments, and other contract documents ⢠Execute contracts against planned timelines and targets ⢠Manage contract budget grids and ensure cost calculations align with protocol and site agreements ⢠Perform quality checks of approved contract and budget documents and initiate signature processes ⢠Ensure contracts meet timelines, Fair Market Value, legal, and regulatory requirements ⢠Serve as primary contact among Clinical Business Operations, Global Clinical Operations, Legal, investigator sites, and external service providers ⢠Collect and maintain country and site intelligence and prepare site-specific contract process flows ⢠Forecast, track, and communicate contract execution dates, changes, and risks ⢠Review and update contract templates and contribute to Legal Playbook guidance ⢠Coordinate with Investigator Payment Management to ensure site contracts and budgets are approved and executed ⢠Ensure investigator contracts receive required legal approval before execution ⢠Maintain communication with site personnel and internal partners throughout the contract lifecycle ⢠Prepare amendments, notes to file, and related documents ⢠Escalate contracting issues and potential delays ⢠Participate in investigator site, project, and department meetings ⢠Maintain CBO trackers, contract document filing and distribution, and Contract Management System records ⢠Provide handoff to the project/payment team
⢠Experienced professional ⢠Highly motivated and collaborative ⢠Ability to draft, negotiate, and finalize complex clinical site contracts ⢠Ability to manage priorities effectively in a fast-paced environment with short deadlines and quick turnaround times ⢠Understanding of records management requirements for contract documents ⢠Knowledge of Fair Market Value and relevant legal and regulatory requirements ⢠Ability to communicate legal and budgetary issues to internal and external parties ⢠Ability to perform legal translation of contract language for sites ⢠Analytical thinking/data analysis ⢠Financial excellence ⢠Clear communication ⢠Demonstrates initiative and continuous learning ⢠Results-oriented and adaptable to change
Apply Nowđ July 13
Senior Site Contract Associate at IQVIA Biotech supporting contracting activities for clinical trials across Europe. Collaborating with sponsors and managing project timelines to ensure compliance and efficiency.