站点合同经理
Site Contracts Manager
Precision for Medicine 正在寻找一位站点合同经理加入我们的欧洲团队。该职位可完全远程办公，工作地点为波兰、斯洛伐克、西班牙、塞尔维亚、罗马尼亚或匈牙利。
职位概述：
审核、起草、谈判并跟踪各种法律协议，包括保密协议、主保密协议、临床研究协议和修订协议。与临床运营研究团队紧密合作，发挥关键作用，确保交付物符合定义的研究时间表。
主要职责包括但不限于：
- 审核、起草和谈判各种协议，包括主服务协议、站点合同、咨询协议、供应商协议、保密协议和其他客户合同。
- 与主管及内部/外部关键利益相关者合作，解决或升级合同问题。
- 确保遵守公司政策、流程和合同标准。
- 向相关研究团队成员通报合同谈判和执行的进展情况。
- 建立、跟踪、报告和管理站点合同指标。
- 支持合同文件和数据库的维护，包括合同归档。
- 协助设计和实施政策和流程，以确保合同及时执行。
- 识别流程改进的机会并采取纠正措施。
- 完成其他指派的任务。
任职要求：
最低要求：
- 本科、研究生或四年制大学学位
- 在CRO/医疗保健领域有工作经验
- 具有起草、审核和谈判站点临床试验协议、供应商合同和站点预算谈判的相关经验，且不少于5年经验。
优先考虑：
- 法学、科学领域、工商管理或同等学位的学士学位
- 优秀的组织和沟通能力，注重细节
- 熟悉制定合同计划——CTA和预算谈判指南
- 成功处理与研究团队和/或CRAs/启动专员/(S)BSCA的关系，以满足研究时间表
技能与素质：
- 拥有强大的组织/书面沟通能力，能够在快节奏环境中多任务处理并优先排序。
- 能够在时限内完成任务，同时保持准确性和细致。
- 展现出高度的自我驱动力和主动性。
查看英文原文
Precision for Medicine is looking for a Site Contracts Manager to join our European Team. The position can be covered fully remotely from the Poland, Slovakia, Spain, Serbia, Romania or Hungary.
Position Summary:
Review, draft, negotiate and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements. Work closely with Clinical Operations study team and play a key role to ensure deliverables are in alignment with defined study timelines.
Essential functions of the job include but are not limited to:
- Review, draft and negotiate a variety of agreements including master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements, and other client contracts.
- Work with supervisor and various internal/external key stakeholders to resolve/escalate contractual issues.
- 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.
- 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.
- Other tasks as assigned.
Qualifications:
Minimum Required:
- Graduate, postgraduate, 4-year college degree
- Experience in a CRO/healthcare field
- Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations, but no less than 5 years’ experience.
- Experienced leading interactions with Study Teams and Sponsor
Preferred:
- Bachelors in law, scientific fields, business administration or equivalent degree
- Excellent organizational and communication skills and attention to detail
- Knowledgeable on setting up Contracting Plans - Guides for CTA & Budget negotiations
- Successful handling relationship study team and/or with CRAs/Start-up Associate/(S)BSCA to meet study timelines
Skills and Competencies:
- Possesses strong organizational/written communication skills and the ability to multi-task and prioritize in a fast-paced environment.
- Executes time-sensitive matters while maintaining accuracy and attention to detail.
- Exhibits high self-motivation and is able to work and plan independently as well as in a team environment.
- Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and teammates, including good interpersonal skills.
- Displays sound business judgment and a proactive, independent work style.
- Proficient in MS Office software programs and computer applications
- Handles sensitive issues with discretion.
- Works well independently and cooperatively with others to achieve common goals in a virtual environment.
- Develops, maintains, and strengthens relationships with others inside or outside of the organization who can provide information, assistance, and support.
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