Contract Associate Clinical Trial
As a Clinical Contracts Associate, you will be responsible for:
Adapting budget templates to local and site-specific requirements.
Drafting, reviewing, and negotiating contracts, amendments, and work orders.
Analyzing documents for corporate risk and proposing appropriate solutions.
Negotiating with research sites in line with internal policies and applicable regulations.
Coordinating with Legal and other internal stakeholders regarding contract terms such as confidentiality, liability, intellectual property, etc.
Reviewing and approving translations in informed consent documents related to injury, privacy, and compensation.