高级合同专员,临床机构合同
Senior Contract Associate, Clinical Site Contracts
BeOne持续以快速的速度增长,为有经验的专业人士提供具有挑战性和令人兴奋的机会。在考虑候选人时,我们寻找具有高度积极性、协作精神,并且最重要的是,对抗击癌症充满热情的科学和商业专业人士。
职位概述:
高级合同专员负责起草、谈判并最终确定与临床试验相关的复杂临床机构合同,贯穿研究的整个生命周期,并及时准确地将数据录入所有临床业务运营系统,包括但不限于公司合同管理系统(CMS)。合同专员还需确保以高质量完成交付成果,并在项目时间表内完成。由CBO团队支持的合同活动节奏快,截止日期短,因此合同专员必须能够有效管理优先级,主动沟通问题,并在快节奏的环境中工作。
岗位核心职责:
- 通过与机构的直接沟通,准备、谈判并最终确定公司资助研究的临床试验协议、附属协议及修订文件。
- 对合同按计划的时间表和目标进行执行。
- 管理合同中的预算表格,确保成本计算符合方案要求并与机构达成一致。
- 展示对合同文件记录管理要求的理解。
- 完成最终批准的合同和预算文件的质量检查(QC),并启动指定合同的责任签署方的签署流程。
- 确保最终合同按约定时间交付,在公平市场价格范围内,并符合相关法律和监管要求。
- 作为CBO与全球临床运营(GCO)、法务、研究者机构和外部服务提供商之间的主要联系人,根据研究相关活动满足业务需求;
- 收集并维护每个国家和/或机构的国家和机构情报信息,并根据需要准备国家/机构特定的合同流程;
- 预测、设定、跟踪并沟通已完全执行的合同计划日期,尽一切努力实现设定的计划日期,确保CM和研究团队及时了解变更和/或风险。
查看英文原文
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
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, and performs timely and accurate data entry into all Clinical Business Operations operating systems, including but not limited to the company Contract Management System (CMS). The Contract Associate is also responsible for meeting deliverables with high quality and within the project timelines. The contracting activity supported by the CBO team is fast-paced, with short deadlines and quick turnaround times therefore Contract Associate must be capable of managing priorities effectively, proactively communicating issues and working in a fast-paced environment.
Essential Functions of the Job:
- 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
- Demonstrates an understanding of records management requirements for contract documents
- 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
- Serve as the primary point of contact between CBO and Global Clinical Operations (GCO), Legal,
- Investigator Sites and external service providers in accordance with the study related activities to meet business needs;
- Collect and maintain country and site intelligence information for each country and/or site, and prepares country/site specific contract process flows as needed;
- Forecast, set, track and communicate fully executed contract planned dates, and make all efforts to achieve the set planned date, ensuring the CM and study teams are proactively informed of changes and/or risks to the projected dates;
- Liaise with CM and BeOne Medicines legal to review and update contract template(s) as needed, including Master Clinical Trial Agreements/Clinical Trial Agreements/Project Agreements or any other Site agreement template(s);
- Liaise with CM and BeOne Medicines legal to contribute updates to the BeOne Medicines Legal Playbook guidance document as needed;
- Liaise with Clinical Site Budgets and Payment team to ensure site contracts, including investigator site budgets, are approved and executed in accordance with CBO guidelines and BeOne Medicines policies;
- Ensure all investigator contracts are reviewed and approved by legal and/or delegate prior to execution, and in accordance with CBO and BeOne Medicines legal guidelines;
- Communicate legal and budgetary issues to internal and external parties per department guidelines, as needed;
- Perform legal translation of contract language for Sites, as needed;
- Maintain active and regular communication with site personnel and internal BeOne Medicines partners, with regular progress tracking and updates provided throughout the contract lifecycle;
- Prepare subsequent contract amendments, note to files and other related contract documents, as needed;
- Escalates contracting issues and/or potential delays to internal and external stakeholders, as necessary;
- Attend and actively participate in Investigator Site, project related, CBO, and other meetings, as necessary;
- Update and maintain CBO trackers with real-time updates on a regular basis, complete CBO related filing and distribution of contract documents, and maintain Contract Management System (CMS) records, in accordance with CBO and BeOne Medicines policies;
- Provides a handoff to the project/payment team upon execution of a site’s final contractual documents
Supervisory Responsibilities: none
Computer Skills:
· Microsoft Office apps, CTMS, Contract Lifecycle Management System, Veeva, Jira, Sharepoint etc.
Other Qualifications:
- Good knowledge of ICH-GCP, pharmaceutical related regulations and laws;
- Good understanding of clinical trial contracting process, and relevant clinical operation • practices;
- Awareness and understanding of compliance and regulatory matters in clinical research
- Proven negotiation, interpersonal and business skills
- Strong planning and organizational skills and the ability to work independently and effectively in a dynamic environment with competing priorities
- Sense of urgency and strong goal orientation; track-record of meeting deadlines and goals
- Strong written and verbal communication including written and verbal fluency in English and local language (if not English) and interpersonal skills, including conflict resolution and problem solving.
- Proactive and positive team player. Able to maintain high performance during times of ambiguity and change in the work environment.
- Experience in financial, budget, cost management/analysis, accounting, and/or financial planning skills are desirable
- Has knowledge of Intellectual Property issues, Publication issues, Indemnification issues and other standard issues of site contracts within the clinical research area.
- Must be willing to work in a fast-paced environment with time-sensitive material.
- Demonstrated ability to work effectively at all levels of an organization.
Travel: Yes, 10%
Salary Range Spain: 57,600.00 EUR - 72,000.00 EUR
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
- Fosters Teamwork
- Provides and Solicits Honest and Actionable Feedback
- Self-Awareness
- Acts Inclusively
- Demonstrates Initiative
- Entrepreneurial Mindset
- Continuous Learning
- Embraces Change
- Results-Oriented
- Analytical Thinking/Data Analysis
- Financial Excellence
- Communicates with Clarity
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.
Originally posted on Himalayas