Senior Site Contracts Manager - FSP

  Precision for Medicine is looking for a Senior Site Contracts Manager to join our FSP group in Europe. We are looking for someone with extensive site contracts and budgets experience across European region. This position can be covered fully remotely from France. Position Summary:  Review, draft, negotiate and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendments. Works closely with Clinical Operations study teams and plays a key role to ensure deliverables are in alignment with defined study timelines. The Senior Contracts Manager will serve as a subject matter expert within the department and company regarding site contract management..  Essential functions of the job include but are not limited to:   Establish process and procedures for overall site contract management in the organization. Review, draft and negotiate a variety of agreements including site contracts, confidentiality agreements, and other client contracts. .   Escalate and resolve complex issues with clients and internal stakeholders. Negotiate site budget. Provide guidance to business teams regarding operational implications of contract terms. Ensure adherence to company policies, procedures and contracting standards. Update relevant study team members regarding the status of contract negotiations and execution. Establish, track, report and manage site contract metrics. Coordinate execution of agreements and track agreement expirations and other obligations Support the maintenance of contract files and databases, including contract archiving. Assist in designing and implementing policies and procedures to affect the timely execution of contracts. Recognize where processes can be improved and take corrective action. Mentor and/or Ambassador for new SCMs and Precision for Medicine staff Other tasks, as assigned. Qualifications:  Minimum Required:  Graduate, postgraduate, 4-year college degree  Equivalent experience ideally in a scientific or healthcare discipline  Previous CRO experience 5+ years Oncology experience Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements and site Budget negotiations, but no less than 7 years’ experience.  Experienced leading interactions with US/European/APAC or other regions institutions Experienced leading interactions with Study Teams and Sponsor Fluent in French and English  Preferred:  Bachelors in law, scientific fields, business administration or equivalent degree  Excellent organizational and communication skills and attention to detail  Experienced on setting up Contracting Plans - Guides for CTA & Budget negotiations  Experienced dealing with Kick-Off Meetings (KOM) and Bid Defense Meetings (BDM) Successful handling relationship study team and/or with CRAs/Start-up Associate/(S)BSCA to meet study timelines ...