The Senior Contract Associate is responsible for drafting, negotiating, and finalizing complex Clinical Site Contracts related to clinical trials throughout the lifecycle of the study, with focus on the United Kingdom market.
- Prepare, negotiate, and finalize clinical trial agreements, ancillary agreements and amendments of company sponsored studies through direct communication with sites.
- Responsible for execution of contracts against planned timelines and targets.
- Manage budget grid in the contract. Ensure the cost calculation are consistent with protocol and agreed with site
- Complete quality check (QC) of final approved contract and budget documents, and initiates signature process of assigned contracts to the responsible signing parties.
- Ensure final contracts are delivered to agreed timelines, within Fair Market Value & in compliance with relevant legal and regulatory requirements
- Bachelor's degree
- Nice to have: Legal or administrative management education background
- Nice to have: Experience in pharmaceutical company
- Nice to have: Experience in biotechnology, pharmaceutical, and/or CRO industry
- Nice to have: Strong negotiation skills
