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。该职位可从波兰、斯洛伐克、西班牙、塞尔维亚、罗马尼亚或匈牙利远程办公。
职位简介：
审查、起草、谈判并跟踪各种法律协议，包括保密协议、主保密协议、临床研究协议和修改协议。与临床运营研究团队紧密合作，并在确保交付成果符合定义的研究时间表方面发挥关键作用。
岗位主要职责包括但不限于：
- 审查、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/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程序，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。
- 其他指派的任务。
任职要求：
最低要求：
- 本科或研究生学历，四年制大学学位
- 在 CRO/医疗保健领域有工作经验
- 有起草、审查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，但至少需要 5 年经验。
- 有与研究团队和申办方进行互动的经验
优先考虑：
- 法律、科学、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，能够在快节奏的环境中多任务处理并优先排序。
- 能够处理时效性强的事务，同时保持准确性和细致入微的关注。
- 展现出高度的自我驱动力，是
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.
Reasonable estimate of the current range for Poland: 190,200 - 237,800 PLN
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at .
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Originally posted on Himalayas