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Site Contracts Associate II at Parexel
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient.
We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities : SCA Tasks Draft, review and negotiate all site agreements including but not limited to clinical study agreements, service agreements, team member agreements and other types of related documents like letters, notices, etc.
Provide context to comments received from sites in light of local legal and business framework, common practices, and past negotiation experience for the purpose of further review up the decisioning chain Apply and scrutinize site contract and related documents and their revisions against negotiation and budget parameters (as applicable) Ensure final documents comply with applicable laws, regulations, and guidelines, including ICH – GCP Ensure the best interest of both clients and Parexel are met Serves as key communication liaison between site contracts staff and internal and external customers.
Provides functional guidance and keeps internal and external teams aware of all contract statuses or pending issues. Prepares correspondence as necessary.
Manage the contract execution process, including obtaining required signatures and ensuring timely execution of the document by all parties Follow record maintenance and archival guidelines to ensure they are met Develop and maintain positive relationships with clinical trial sites Develop and maintain a thorough understanding of the clinical trial protocol, budget, and timelines to ensure that contract terms align with the overall trial goals and objectives Identify potential issues or concerns with contract terms and collaborate with internal stakeholders and clinical trial sites to find mutually acceptable solutions Stay up to date with relevant regulatory
Requirements
, law, economics, business, social sciences), equivalent training or industry experience ATS provider: Workday.